Mediators of Inflammation

Mediators of Inflammation / 2019 / Article

Review Article | Open Access

Volume 2019 |Article ID 7894017 | 10 pages | https://doi.org/10.1155/2019/7894017

Search for Novel Diagnostic Biomarkers of Prostate Inflammation-Related Disorders: Role of Transglutaminase Isoforms as Potential Candidates

Academic Editor: Oleh Andrukhov
Received31 Jan 2019
Accepted13 Jun 2019
Published09 Jul 2019

Abstract

Investigations on prostate inflammation-related disorders, including acute and chronic prostatitis, chronic pelvic pain syndrome, benign prostate hyperplasia (BPH), and prostate cancer (PCa), are still ongoing to find new, accurate, and noninvasive biomarkers for a differential diagnosis of those pathological conditions sharing some common macroscopic features. Moreover, an ideal biomarker should be useful for risk assessment of prostate inflammation progression to more severe disorders, like BPH or PCa, as well as for monitoring of treatment response and prognosis establishment in carcinoma cases. Recent literature evidence highlighted that changes in the expression of transglutaminases, enzymes that catalyze transamidation reactions leading to posttranslational modifications of soluble proteins, occur in prostate inflammation-related disorders. This review focuses on the role specifically played by transglutaminases 4 (TG4) and 2 (TG2) and suggests that both isoenzymes hold a potential to be included in the list of candidates as novel diagnostic biomarkers for the above-cited prostate pathological conditions.

1. Introduction

Prostate is classified as an immune-competent organ, being populated by leukocytes, including stromal and intraepithelial T and B lymphocytes, macrophages, and mast cells; notably, the number of leukocytes increases with aging [1]. In retrospect, it is significant to note that reviews of immunobiological studies of the prostate and patients with diseases thereof (the latest of which is [2]), including observations and suggestion of the existence of a local immunological system, i.e., “prostate lymphoreticular system,” ergo “being classified as an immune-competent organ” [1], were made prior to more contemporary observations. In the last decades, clinical trials and epidemiological observations have shown that prostate inflammation is a common condition in aged men [35].

Prostate inflammation is classified through histological evaluation of the amount of inflammatory cells and their effect on prostate tissue [6]. The prostate inflammatory process may be triggered through different molecular pathways of the immune system, which are dysregulated secondarily to different factors: infectious bacterial agents, viruses, or other sexually transmitted microorganisms, urinary reflux, aging, dietary factors, hormones, autoimmune response, or a combination of these factors [1, 2, 7, 8].

Inflammation is typically distinguished as acute (neutrophilic cell infiltrate) and chronic (mononuclear cell infiltrate) [9]. Prostate inflammation may become a chronic process when the microorganism causing acute prostatitis is not eradicated.

Chronic prostatitis (CP) is a clinical syndrome, affecting 10% of the male elderly population, characterized by lower genitourinary tract and/or genital pain or discomfort and by inflammatory cells in prostatic secretions [10]. It has also been defined as CP/chronic pelvic pain syndrome (CP/CPPS) since it is not always caused by an infection. The presence of mononuclear inflammatory cells in the prostate is not diagnostic for CP/CPPS, and other inflammatory cells, such as T-cells, are commonly detected [4].

Chronic inflammatory processes are accompanied by the release of large amounts of proinflammatory cytokines, as well as oxygen and nitrogen reactive species (ROS and RNS). Oxidative stress plays a key role in the pathogenesis of CP/CPPS [11]. Cell response to both inflammation and oxidative stress involves the activation of transcription factor nuclear factor-kappa B (NF-κB), leading to the upregulation of genes encoding for proinflammatory cytokines, the levels of which are further increased, as well as chemotactic factors and growth factors [12]. Several evidences show the presence of oxidative stress markers in the secretions of the genitourinary tract in patients affected by prostate inflammation [11].

Notably, chronic prostate inflammation is a process that could lead to the development of more severe prostatic disorders, like benign prostatic hyperplasia and prostate cancer, and also of the genitourinary tract [1, 2, 1317].

Benign prostatic hyperplasia (BPH), the most common urological disorder in 70-80-year-old men [18], is a chronic progressive condition due to a nonmalignant propagation of stromal and epithelial cells eventually leading to prostate enlargement, associated with the development of nodules and proliferative inflammatory atrophy [19]. The pathogenesis and progression mechanisms of BPH are still not well characterized, but they likely involve several factors, i.e., changes in epithelial-stromal interactions, alterations of local endocrine and autonomous nerve system, tissue damage, and subsequent chronic tissue healing. Some authors have assimilated BPH to an immune-mediated inflammatory disease [13, 14, 2022], others suggested a relationship between prostatic inflammation and lower urinary tract symptoms (LUTS) [3, 4] and/or other promotional factors common to BPH and PCa [14].

Prostate cancer (PCa) is considered as a chronic disease and the most prevalent cancer in the male population [23]. Epidemiological studies suggest that PCa is hormone-dependent and is associated with inflammation, as suggested by the detection of PCa susceptibility genes involved, such as RNAseL, MSR1, TLR4, MIC1, PON1, BRCA2, CHEK2, and OGG, which have a role in prostate carcinogenesis, and also in the host response to infection, inflammation, and oxidative stress [24, 25]. However, there is not a clear evidence showing that a reduction of PCa incidence and progression may be achieved through inhibition of prostate inflammation [26].

In the last years, great efforts have been undertaken to identify novel biomarkers that, alone or combined with the calculation of risks for the progression of prostate inflammation to BPH or PCa, may reduce the need for unnecessary biopsies, improve the stratification of low-risk patients, and better predict the response to treatments. Moreover, ideal biomarkers should also be able to accurately discriminate between indolent and aggressive cancers and identify men at high risk for developing PCa that require immediate treatment [27].

Several lines of evidence suggest that a key role in inflammatory processes and in the inflammation-induced progression of several types of cancers is played by transglutaminase 2 (TG2) or tissue transglutaminase. TG2 is an ubiquitous member of the transglutaminase (TG) family of enzymes, that catalyze calcium-dependent transamidation reactions through the incorporation of amines to glutamine residues (polyamination) or cross-linking of lysine residues to glutamine residues, resulting in the formation of intra- and intermolecular, covalent ε-(γ-glutamyl)lysine isopeptide bonds [28]. The involvement of TG2, and also transglutaminase 4 (TG4), another member of TGs that is uniquely distributed in the prostate gland, has been reported in BPH and PCa [2934].

This review will summarize available literature data on biomarkers of prostate disorders and discuss the role of TG isoforms as potentially novel diagnostic biomarkers of prostate inflammation-related diseases.

2. Current Biomarkers of Prostate Disorders

The first biomarker of prostatitis condition was the white blood cell (WBC) count in prostatic secretion, but then, it was discarded due to its poor sensitivity [35]. The assessment of serum levels of prostate specific antigen (PSA), a member of the kallikrein gene family, is still carried out for PCa screening, even though the classification of PSA as a PCa biomarker has become increasingly controversial due to the lack of specificity [36]. Suspicious digital rectal examination and/or a , usually considered as criteria to prompt further evaluation for PCa [37], has been the subject of increasingly false positives and overdiagnosis. For instance, the increase of serum PSA levels has also been correlated with the aggressiveness of histological inflammation [38]. The low specificity of this test may be due to the presence of different PSA isoforms, since alternative splicing and alternative polyadenylation lead to the formation of at least 15 PSA transcripts, encoding for at least eight different proteins [39]. An investigation about the changes of these spliced variants in PCa is required for more specific PSA screening tests. Notably, several alternatively spliced isoforms of other kallikreins (KLK2, KLK3, KLK11, and KLK15) have been shown to be upregulated in PCa [40].

Chronic inflammation has been associated with the severity of lower urinary tract symptoms (LUTS), higher International Prostate Symptom Score (IPSS), and higher prostate volume if compared to prostate in normal conditions [41, 42]. Even though less invasive methods are used to assess the risk of developing prostatic chronic inflammation, such as detection of circulating biomarkers or imaging, the unique instrument to make a diagnosis of CP remains the histological exam [6, 43]. In prostate biopsies, the Chronic Prostatitis Symptom Index (CPSI) is utilised to highlight prostatitis-like symptoms, such as pain and burning sensation, dribbling and hesitant urination, urgency, or painful ejaculations. In fact, the total CPSI score is significantly associated with chronic inflammation. Moreover, patients with CP/CPPS are evaluated with UPOINT (urinary, psychosocial, organ-specific, infection, neurogenic, and tenderness) categorization [44].

A further diagnostic feature is the presence of prostatic calcifications, which increase progressively with aging, and the incidence of which has significantly been associated with greater inflammation and protracted symptoms in patients with CPPS [4547].

One of the most reliable prostatic inflammation markers is the level of IL-8 in seminal plasma [48, 49], even in comparison with other cytokines [35, 50]. Another experimental marker of prostatic inflammation is the urinary level of inducible T-cell costimulator (ICOS) protein involved in cell signaling, immune response, and cell proliferation, that has been significantly associated with maximum uroflowmetry and postvoid residual urine volume [41]. Furthermore, the involvement of monocyte chemotactic protein-1 (MCP-1) has been hypothesized in the pathogenesis of CP and BPH, as its increase in prostatic secretions is associated with prostate volume enlargement and the expression of the macrophage marker CD-68 [51, 52].

CP has also been associated with autoimmune responses against prostate antigens, including prostatic acid phosphatase (PAP), prostate steroid-binding protein (PSBP), PSA, and other antigens in prostate homogenates and seminal plasma [5355].

PCa may present with both aggressive and indolent forms. Given that low-grade prostate cancer is clinically insignificant and usually not associated with metastatic dissemination, a common practice for the management of patients with “low risk” or “favorable risk” is active surveillance. This practice is appropriate for men having PSA levels lower than 10 ng/mL and involves the periodic monitoring of patients through serial PSA testing, digital rectal exam, and biopsy sampling [56].

The hardest challenges in the clinical practice are the right selection of patients eligible for biopsy intervention, the differentiation of indolent tumors from those with an unfavorable prognosis, and the early recognition of higher-risk disease in patients initially diagnosed with low-risk disease and monitored by active surveillance. Current diagnostic biomarkers of PCa include blood-based tests, such as ProstateHealth Index® and 4K score®, other than PSA; urine sample-based tests, i.e., prostate cancer antigen 3 (PCA3), SelectMDx®, and ExoDx Prostate IntelliScore®; and tissue-based tests (ConfirmMDx®, Oncotype®, Prolaris®, and Decipher®) following biopsy, transurethral resection, or radical prostatectomy [27].

3. Role of Transglutaminase 4 in Prostate Disorders

Transglutaminase 4 (TG4) was discovered in the early 1990s from a human prostate cDNA library [57]. Its physiological role has firstly been defined in rodents as a regulator of copulatory plug formation [58], which is relevant for the fertilization, as it allows the seminal fluid to be kept in the vagina [59]. Via the incorporation of seminal proteins, such as uteroglobin, semenogelins, or polyamines, into sperm cell surfaces, TG4 suppresses sperm antigenicity in the female genital tract [6062]. The typical TG substrates, polyamines, in particular putrescine, spermidine, and spermine, are secreted by the prostate gland and released in the seminal fluid. In mice and humans, seminal plasma is rich in spermidine and spermine of prostatic origin which may regulate at the urethra level the seminal clot formation during the ejaculatory process [58]. Seminal vesicles, thus even in secretions, have demonstrated intermediate TG activity and low polyamine amount. Notably, the level of protein-bound polyamines in ventral and anterior prostate suggests a higher extracellular activity of prostatic TG and polyamines. Furthermore, Km values of rat prostate TG for all the polyamines confirm the regulatory role of polyamines in the formation of the seminal clot [63]. Interestingly, the presence of autoantibodies against TG4 in association with human male infertility has recently been demonstrated, suggesting that TG4 plays a key role in the fertilization competence of spermatozoa [64, 65].

The role of TG4 in humans is still not well characterized. Human TG4 is a secretory protein having an expression pattern restricted to the prostate, where it has been found in luminal epithelial cells. TG4 is released in the seminal fluid and responds to androgen stimulation [66, 67]. In this regard, evidence has been provided that the retinoic acid receptor gamma (RAR-G) plays a major role in the regulation of TGM4 and that the presence of the androgen receptor (AR), but not its transcriptional transactivation activity, is critical for TGM4 transcription [68].

It has been reported that some human prostate cancer cell lines lack TG4 expression [66], even if a basal transcriptional activity of the promoter was observed [69]. Results from an analysis of TG4 transcripts in metastatic prostate cancer specimens indicate that TG4 expression was reduced in most of them [70]. The downregulation of TG4 expression in prostate cancer was confirmed by histological analyses of its distribution within sections from tumor-containing prostatectomy specimens and needle biopsies. The staining was restricted to luminal epithelial cells and not detected in basal epithelial or stromal cells. Moreover, TG4 staining was detected in high-grade prostatic intraepithelial neoplasia specimens but not in prostate carcinoma cells [67].

Other data have shown that TG4 knockdown is correlated with a lowered invasive ability of prostatic cancer cells [71]. TG4 expression showed a relatively wide profile in different prostate cancer cell lines and was strongly induced in the low invasive CA-HPV-10 prostate cancer cell line [71]. Thus, TG4 can be involved with the invasiveness of prostate cancer cells. A similar result was reported by Jiang and coworkers showing TGM4 overexpression in a human prostate tumor compared to normal tissue and a higher expression in high-Gleason score tumors [31].

In a mouse prostate cancer model generated by deletion of the prostate epithelium-specific tumor suppressor PTEN, TGM4 was rapidly downregulated and the dedifferentiation of the prostatic epithelium was quicker than in organ-confined human prostate cancers [72]. Other studies have revealed that TG4 overexpression in prostatic cells increases the adhesion of tumor cells to endothelial cells and decreases the barrier function of the latter. Moreover, TG4 sensitizes prostate cells to hepatocyte growth factor (HGF) [73].

These contradictory results may be explained taking into account that different studies may have addressed their efforts in the search for the classical TG4 form. However, proteins obtained by an alternative splicing mechanism acquire, in part, different structural and functional features compared to the original proteins [74]. These modifications are likely responsible for the failure of RT-PCR, Western blot, and immunohistochemical techniques aimed at detecting the classical TG4 form. Indeed, Cho and coworkers found four mRNA variants (L, M1, M2, and S) in the prostatic tissue of patients affected by BPH and PCa [32]. TG4-M1 and TG4-M2 have different splicing sites but not nucleotide size. Moreover, TG4-L, TG4-M1, and TG4-M2 have correct open reading frames, whereas TG4-S has a truncated reading frame (Figure 1(a)); however, the role of alternative splicing variants in prostate tissue is not well known.

Notably, TG4-M and TG4-S were detected in all tested BPH and PCa prostate tissues, while TG4-L was found in 56% of BPH and only in 15% of PCa. These findings suggest that changes in alternative splicing correlate with the development of PCa. However, TG4-L expression did not correlate with PSA serum levels, prostate volumes, or PSA densities [32]. Interestingly, although TG4 expressed in HeLa cells has been found as a secreted protein, TG4-L has not been detected in the supernatant of cell cultures [32]. The different cellular localizations suggest a different role for the spliced variants since they likely use different protein substrates, raising the idea that TG4 splicing variants may be exploited as diagnostic and/or therapeutic targets, as seen before for other genes in several cancers [75].

TGM4 expression levels were lower in moderately or poorly differentiated carcinoma compared with normal tissue [76]. Western blot analysis together with immunohistochemical analysis demonstrated TGM4 downregulation in prostate cancer [77]. Then, the comparison of protein markers in prostatic secretions of men having organ-confined tumors or extracapsular tumors showed differential expression of TG4, PSA, ANXA3, and matrix metalloproteinases (MMP7 and 9) between the two groups [78].

TG4 resulted also to be involved in cancer disease progression via promotion of epithelial-mesenchymal transition (EMT). In fact, in prostate epithelia-derived cancer cells, loss of E-cadherin, acquisition of N-cadherin, and cell migration have been highlighted [79].

4. Role of Transglutaminase 2 in Prostate Disorders

TG2 is a multifunction protein, since other than acting as a transamidating enzyme, it also displays GTPase, protein disulfide isomerase, kinase, cell adhesion, and scaffolding activities [80].

The function of TG2 in prostate is not fully understood yet. Unlike the prostate-specific TG4, TG2 is ubiquitous in prostatic tissue and is predominantly present in the intracellular compartment [57, 81]. Likely, TG2 is a pivotal component of cell signaling because it modulates the activation of the alpha1-adrenergic receptor, which mediates prostatic smooth muscle contraction [82].

Numerous inflammatory cytokines and growth factors stimulate TG2 expression, such as IL-1, IL-6, TNF-α, and TGF-β [8385], due to the presence in TGM2 gene promoter of different regulatory sites for inflammatory modulators, NF-κB response element (-1338 bp), IL-6 specific cis-regulatory element (-1190 bp), and TGF-β1 response element (-868 bp). TG2 overexpression, in turn, has been reported to constitutively activate and extend NF-κB activation through IκBα polymerization and degradation (Figure 2), in chronic inflammatory conditions and in cancer cells [8688].

TG2 protein and mRNA expression have been evaluated in experimental models of castration-induced prostatic atrophy with subsequent testosterone-induced prostatic hyperplasia. TG2 protein was strongly expressed and correlated with apoptosis. TG2 mRNA levels were not affected during the process of prostate involution but increased early in association with testosterone-induced proliferation [89]. Interestingly, in men treated with finasteride, a 5 alpha-reductase inhibitor, to reduce prostate size and ameliorate BPH symptoms, prostate involution has been shown to occur through both atrophy and cell death processes, in which TG2 has been demonstrated to play a relevant role [90].

Whey-acidic-protein four-disulfide core (WFDC) proteins play a major role as regulators of innate immunity, antimicrobial function, and inhibition of inflammatory proteases at mucosal surfaces. The prostate stromal 20 (ps20), a protein of the WFDC family, is a potent growth inhibition factor, which is also able to modulate the wound healing process and immune response. It has recently been shown that the posttranslational processing and cleavage of ps20 are required to generate a functional protein species and that TG2 mediates the cross-linking and cathepsin L cleavage to form components of a ps20 regulatory apparatus [91].

Cancer cells have been reported to express elevated levels of TG2; moreover, TG2 expression is further highly enriched in cancer-derived stem cells and promotes their survival [92]. However, conflicting results have been reported about the role of TG2 in PCa.

Despite the fact that TG2 was first suggested as a marker of apoptosis during treatment and progression of PCa [29], likely other mechanisms play a more relevant role in the prostate. Birckbichler and coworkers suggested that if all epithelial cells in prostate benign samples are immunoreactive for TG2, it is possible that the TG2 main function is not the promotion of apoptosis [93]. Interestingly, immunohistochemistry analysis demonstrated that TG2 expression is decreased in malignant glands as compared with benign or hyperplastic glands [93]. This study suggested the potential use of TG2 loss in prostate tissue as a potential biomarker for differentiation of PCa from BPH or other inflammatory conditions. Other than for diagnosis, the determination of TG2 levels could be useful for individual risk assessment and patient monitoring [93].

On the other hand, a strong interaction between protein kinase A anchor protein 13 (AKAP13) and TG2 has been reported in prostate cancer. Since AKAP plays a major role in protein kinase A and Rho protein-mediated signaling, the TG2-AKAP13 interaction has been suggested to play a role in prostate cancer [30].

Advanced prostate cancer is often associated with reduced androgen receptor (AR) expression leading to castration-resistant cancer [94]. In the physiological response to androgens, the AR binds to androgen-response elements (AREs) to modulate gene transcription. The transcription factor Oct1 is a context-dependent negative coregulator of AR. Notably, siRNA knockdown of Oct1 increases the transcription of TGM2, an endogenous AR target gene. Therefore, Oct1 may have regulatory functions in prostate development and cancer progression [95]. Recent studies demonstrated high TG2 basal levels in advanced prostate tumor cells showing a reduced AR expression. Notably, TG2 was shown to negatively regulate the AR level. In particular, TG2-mediated NF-κB activation is able to induce NF-κB binding to DNA elements in the AR gene, which in turn reduces AR gene expression [34].

Recently, an interesting role of TGM2_v2 (according to rationalized nomenclature [96]) or TG2 short form has been highlighted in prostate cell lines or specimens. TGM2_v2 mRNA is obtained from an alternative splicing event with an intron retention mechanism of intron X, and it encodes for a 548 aa (63 kDa) protein. The loss of a portion of the C-terminal domain (Figure 1(b)) decreases affinity for GTP, resulting in the escape from the negative control mediated by GTP on TG activity when there is a transient Ca2+ increase [97]. Interestingly, it has been reported that canonical and alternative TG2 isoforms are all expressed in normal human prostate tissue, even if the relative amount of TGM2 shorter transcript is small compared with a full-length one (TGM2_v2 10% vs. 90% TGM2_v1). Alternative splicing of TGM2 occurs differently in cancer cell lines, and in prostate cancer cells the alternative splicing of TG2 is a more active process. Indeed, the average expression levels of TGM2_v2 were found to be higher than that of the long classic transcript (TGM2_v1) in a small screening of prostate cancer tissues compared with normal tissues [96].

On the other hand, the differentiation treatment with γ-tocopherol of prostate carcinoma PC3 cells induced a decrease in the progression into the S-phase, which was associated with TG2 upregulation and increased activity, significant decrease of DNA synthesis, and protein expression of cyclins D1 and E. TG2 upregulation and activation could be part of a larger pathway that promotes the attenuation of prostate cancer malignancy [98].

5. Conclusions

In the last years, evidence has been provided that human TG4 and TG2 are alternatively spliced in prostate tissues and that alternative splicing processes occur in association with loss of prostate tissue homeostasis and transition towards pathological states, i.e., inflammatory conditions and cancer. This issue needs to be carefully addressed and become object of further investigations aimed at better understanding whether differential alternative splicing may represent a signature of specific prostate disorders. In fact, results from these investigations would open new diagnostic perspectives, particularly if TG4 and TG2, and their alternative variants, could be detected in serum samples from patients.

It is well known that TG4 is released in seminal plasma. Although the presence of TG4 in serum has not been investigated, the detection of autoantibodies against TG4 in the serum of male patients affected by infertility [64] suggests that TG4 could also move from seminal plasma to serum. If this was confirmed, the detection of TG4 and its alternatively spliced forms in the serum of patients with prostate disorders could be helpful in discriminating between prostate benign inflammatory conditions and malignant conditions. However, if the TG4 presence was only restricted to seminal plasma, the assessment of different TG4 variants in seminal plasma could be helpful for diagnostic purposes and represent an alternative to biopsy intervention.

TG2 is known to be exported outside the cells, and this event has been reported in inflammatory as well as malignant conditions [80]. However, its presence in the seminal plasma and serum has not yet been investigated. Given that TG2 autoantibodies are abundantly present in the serum of patients affected by celiac disease [99], it is not unreasonable to hypothesize that also TG2, and likely its alternatively spliced variants, may be present either in serum or in seminal plasma. The combined detection of TG4 and TG2 alternative variants in seminal plasma and serum could be a powerful tool for differential diagnosis of prostate disorders.

Conflicts of Interest

The authors declare that they have no conflict of interest.

References

  1. A. M. De Marzo, E. A. Platz, S. Sutcliffe et al., “Inflammation in prostate carcinogenesis,” Nature Reviews Cancer, vol. 7, no. 4, pp. 256–269, 2007. View at: Publisher Site | Google Scholar
  2. R. J. Ablin and T. C. Whyard, “Immunobiological implications of selected bioactive molecules in the prostate with a known and unknown target,” in The Prostate as an Endocrine Gland, W. E. Farnsworth and R. J. Ablin, Eds., pp. 148–172, CRC Press, 1990. View at: Google Scholar
  3. J. C. Nickel, C. G. Roehrborn, M. P. O’Leary, D. G. Bostwick, M. C. Somerville, and R. S. Rittmaster, “Examination of the relationship between symptoms of prostatitis and histological inflammation: baseline data from the REDUCE chemoprevention trial,” The Journal of Urology, vol. 178, no. 3, pp. 896–901, 2007. View at: Publisher Site | Google Scholar
  4. J. C. Nickel, “Inflammation and benign prostatic hyperplasia,” Urologic Clinics of North America, vol. 35, no. 1, pp. 109–115, 2008. View at: Publisher Site | Google Scholar
  5. C. A. St. Hill and M. N. Lutfiyya, “An epidemiological analysis of potential associations between C-reactive protein, inflammation, and prostate cancer in the male US population using the 2009-2010 National Health and Nutrition Examination Survey (NHANES) data,” Frontiers in Chemistry, vol. 3, p. 55, 2015. View at: Publisher Site | Google Scholar
  6. D. M. Moreira, D. M. de O Freitas, J. C. Nickel, G. L. Andriole, R. Castro-Santamaria, and S. J. Freedland, “The combination of histological prostate atrophy and inflammation is associated with lower risk of prostate cancer in biopsy specimens,” Prostate Cancer and Prostatic Diseases, vol. 20, no. 4, pp. 413–417, 2017. View at: Publisher Site | Google Scholar
  7. G. Penna, B. Fibbi, S. Amuchastegui et al., “Human benign prostatic hyperplasia stromal cells as inducers and targets of chronic immuno-mediated inflammation,” Journal of Immunology, vol. 182, no. 7, pp. 4056–4064, 2009. View at: Publisher Site | Google Scholar
  8. G. Penna, B. Fibbi, M. Maggi, and L. Adorini, “Prostate autoimmunity: from experimental models to clinical counterparts,” Expert Review of Clinical Immunology, vol. 5, no. 5, pp. 577–586, 2009. View at: Publisher Site | Google Scholar
  9. J. Irani, P. Levillain, J. M. Goujon, D. Bon, B. Dore, and J. Aubert, “Inflammation in benign prostatic hyperplasia: correlation with prostate specific antigen value,” The Journal of Urology, vol. 157, no. 4, pp. 1301–1303, 1997. View at: Publisher Site | Google Scholar
  10. J. N. Krieger and K. J. Egan, “Comprehensive evaluation and treatment of 75 men referred to chronic prostatitis clinic,” Urology, vol. 38, no. 1, pp. 11–19, 1991. View at: Publisher Site | Google Scholar
  11. A. U. Ihsan, F. U. Khan, P. Khongorzul et al., “Role of oxidative stress in pathology of chronic prostatitis/chronic pelvic pain syndrome and male infertility and antioxidants function in ameliorating oxidative stress,” Biomedicine & Pharmacotherapy, vol. 106, pp. 714–723, 2018. View at: Publisher Site | Google Scholar
  12. G. Paulis, “Inflammatory mechanisms and oxidative stress in prostatitis: the possible role of antioxidant therapy,” Research and Reports in Urology, vol. 10, pp. 75–87, 2018. View at: Publisher Site | Google Scholar
  13. G. Kramer and M. Marberger, “Could inflammation be a key component in the progression of benign prostatic hyperplasia?” Current Opinion in Urology, vol. 16, no. 1, pp. 25–29, 2006. View at: Google Scholar
  14. R. J. Ablin, “Immunological aspects of benign prostatic hypertrophy,” in Benign Prostatic Hypertrophy, F. Hinman and S. Boyarsky, Eds., pp. 73–98, Springer, New York, NY, USA, 1983. View at: Publisher Site | Google Scholar
  15. V. C. Mishra, D. J. Allen, C. Nicolaou et al., “Does intraprostatic inflammation have a role in the pathogenesis and progression of benign prostatic hyperplasia?” BJU International, vol. 100, no. 2, pp. 327–331, 2007. View at: Publisher Site | Google Scholar
  16. K. C. Torkko, R. S. Wilson, E. E. Smith, J. W. Kusek, A. van Bokhoven, and M. S. Lucia, “Prostate biopsy markers of inflammation are associated with risk of clinical progression of benign prostatic hyperplasia: findings from the MTOPS study,” The Journal of Urology, vol. 194, no. 2, pp. 454–461, 2015. View at: Publisher Site | Google Scholar
  17. M. B. Frungieri, R. S. Calandra, A. Bartke, and M. E. Matzkin, “Ageing and inflammation in the male reproductive tract,” Andrologia, vol. 50, no. 11, article e13034, 2018. View at: Publisher Site | Google Scholar
  18. G. Kramer, D. Mitteregger, and M. Marberger, “Is benign prostatic hyperplasia (BPH) an immune inflammatory disease?” European Urology, vol. 51, no. 5, pp. 1202–1216, 2007. View at: Publisher Site | Google Scholar
  19. W. Bushman, “Etiology, epidemiology, and natural history,” Urologic Clinics of North America, vol. 36, no. 4, pp. 403–415, 2009. View at: Publisher Site | Google Scholar
  20. G. Kramer, G. E. Steiner, A. Handisurya et al., “Increased expression of lymphocyte-derived cytokines in benign hyperplastic prostate tissue, identification of the producing cell types, and effect of differentially expressed cytokines on stromal cell proliferation,” Prostate, vol. 52, no. 1, pp. 43–58, 2002. View at: Publisher Site | Google Scholar
  21. G. E. Steiner, U. Stix, A. Handisurya et al., “Cytokine expression pattern in benign prostatic hyperplasia infiltrating T cells and impact of lymphocytic infiltration on cytokine mRNA profile in prostatic tissue,” Laboratory Investigation, vol. 83, no. 8, pp. 1131–1146, 2003. View at: Publisher Site | Google Scholar
  22. G. E. Steiner, M. E. Newman, D. Paikl et al., “Expression and function of pro-inflammatory interleukin IL-17 and IL-17 receptor in normal, benign hyperplastic, and malignant prostate,” Prostate, vol. 56, no. 3, pp. 171–182, 2003. View at: Publisher Site | Google Scholar
  23. R. L. Siegel, K. D. Miller, and A. Jemal, “Cancer statistics, 2016,” CA: A Cancer Journal for Clinicians, vol. 66, no. 1, pp. 7–30, 2016. View at: Publisher Site | Google Scholar
  24. W. G. Nelson, A. M. De Marzo, and W. B. Isaacs, “Prostate cancer,” The New England Journal of Medicine, vol. 349, no. 4, pp. 366–381, 2003. View at: Publisher Site | Google Scholar
  25. A. Alcaraz, P. Hammerer, A. Tubaro, F. H. Schroder, and R. Castro, “Is there evidence of a relationship between benign prostatic hyperplasia and prostate cancer? Findings of a literature review,” European Urology, vol. 55, no. 4, pp. 864–875, 2009. View at: Publisher Site | Google Scholar
  26. C. De Nunzio, G. Kramer, M. Marberger et al., “The controversial relationship between benign prostatic hyperplasia and prostate cancer: the role of inflammation,” European Urology, vol. 60, no. 1, pp. 106–117, 2011. View at: Publisher Site | Google Scholar
  27. A. Carneiro, P. Priante Kayano, Á. R. Gomes Barbosa et al., “Are localized prostate cancer biomarkers useful in the clinical practice?” Tumor Biology, vol. 40, no. 9, 2018. View at: Publisher Site | Google Scholar
  28. M. Griffin, R. Casadio, and C. M. Bergamini, “Transglutaminases: nature’s biological glues,” Biochemical Journal, vol. 368, no. 2, pp. 377–396, 2002. View at: Publisher Site | Google Scholar
  29. R. S. Rittmaster, L. N. Thomas, A. S. Wright et al., “The utility of tissue transglutaminase as a marker of apoptosis during treatment and progression of prostate cancer,” The Journal of Urology, vol. 162, no. 6, pp. 2165–2169, 1999. View at: Publisher Site | Google Scholar
  30. T. E. Lewis, T. D. Milam, D. W. Klingler et al., “Tissue transglutaminase interacts with protein kinase A anchor protein 13 in prostate cancer,” Urologic Oncology, vol. 23, no. 6, pp. 407–412, 2005. View at: Publisher Site | Google Scholar
  31. W. Jiang, R. Ablin, H. Kynaston, and M. Mason, “Expression of the prostate type transglutaminase (TGase-4) in clinical prostate cancer,” Cancer Research, vol. 67, no. 9, pp. 2659–2659, 2007. View at: Google Scholar
  32. S.-Y. Cho, K. Choi, J. H. Jeon et al., “Differential alternative splicing of human transglutaminase 4 in benign prostate hyperplasia and prostate cancer,” Experimental and Molecular Medicine, vol. 42, no. 4, pp. 310–318, 2010. View at: Publisher Site | Google Scholar
  33. W. G. Jiang and R. J. Ablin, “Prostate transglutaminase: a unique transglutaminase and its role in prostate cancer,” Biomarkers in Medicine, vol. 5, no. 3, pp. 285–291, 2011. View at: Publisher Site | Google Scholar
  34. A. L. Han, S. Kumar, J. Y. Fok, A. K. Tyagi, and K. Mehta, “Tissue transglutaminase expression promotes castration-resistant phenotype and transcriptional repression of androgen receptor,” European Journal of Cancer, vol. 50, no. 9, pp. 1685–1696, 2014. View at: Publisher Site | Google Scholar
  35. L. Liu, Q. Li, P. Han et al., “Evaluation of interleukin-8 in expressed prostatic secretion as a reliable biomarker of inflammation in benign prostatic hyperplasia,” Urology, vol. 74, no. 2, pp. 340–344, 2009. View at: Publisher Site | Google Scholar
  36. M. R. Haythorn and R. J. Ablin, “Prostate-specific antigen testing across the spectrum of prostate cancer,” Biomarkers in Medicine, vol. 5, no. 4, pp. 515–526, 2011. View at: Publisher Site | Google Scholar
  37. W. J. Catalona, D. S. Smith, T. L. Ratliff et al., “Measurement of prostate-specific antigen in serum as a screening test for prostate cancer,” New England Journal of Medicine, vol. 324, no. 17, pp. 1156–1161, 1991. View at: Publisher Site | Google Scholar
  38. L. Song, Y. Zhu, P. Han et al., “A retrospective study: correlation of histologic inflammation in biopsy specimens of Chinese men undergoing surgery for benign prostatic hyperplasia with serum prostate-specific antigen,” Urology, vol. 77, no. 3, pp. 688–692, 2011. View at: Publisher Site | Google Scholar
  39. N. Heuzé-Vourc'h, V. Leblond, and Y. Courty, “Complex alternative splicing of the hKLK3 gene coding for the tumor marker PSA (prostate-specific-antigen),” European Journal of Biochemistry, vol. 270, no. 4, pp. 706–714, 2003. View at: Publisher Site | Google Scholar
  40. M. A. Reynolds, “Molecular alterations in prostate cancer,” Cancer Letters, vol. 271, no. 1, pp. 13–24, 2008. View at: Publisher Site | Google Scholar
  41. G. Robert, F. Smit, D. Hessels et al., “Biomarkers for the diagnosis of prostatic inflammation in benign prostatic hyperplasia,” Prostate, vol. 71, no. 15, pp. 1701–1709, 2011. View at: Publisher Site | Google Scholar
  42. J. C. Nickel, C. G. Roehrborn, M. P. O'Leary, D. G. Bostwick, M. C. Somerville, and R. S. Rittmaster, “The relationship between prostate inflammation and lower urinary tract symptoms: examination of baseline data from the REDUCE trial,” European Urology, vol. 54, no. 6, pp. 1379–1384, 2008. View at: Publisher Site | Google Scholar
  43. R. Bardan, R. Dumache, A. Dema, A. Cumpanas, and V. Bucuras, “The role of prostatic inflammation biomarkers in the diagnosis of prostate diseases,” Clinical Biochemistry, vol. 47, no. 10-11, pp. 909–915, 2014. View at: Publisher Site | Google Scholar
  44. R. C. Doiron, D. A. Tripp, V. Tolls, and J. C. Nickel, “The evolving clinical picture of chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS): a look at 1310 patients over 16 years,” Canadian Urological Association Journal, vol. 12, no. 6, pp. 196–202, 2018. View at: Publisher Site | Google Scholar
  45. E. Bock, V. Calugi, V. Stolfi, P. Rossi, R. D'Ascenzo, and F. M. Solivetti, “Calcifications of the prostate: a transrectal echographic study,” La Radiologia Medica, vol. 77, no. 5, pp. 501–503, 1989. View at: Google Scholar
  46. S. E. Lee, J. A. H. Ku, H. K. Park, C. K. H. Jeong, and S. H. Kim, “Prostatic calculi do not influence the level of serum prostate specific antigen in men without clinically detectable prostate cancer or prostatitis,” The Journal of Urology, vol. 170, no. 3, pp. 745–748, 2003. View at: Publisher Site | Google Scholar
  47. D. A. Shoskes, C.-T. Lee, D. Murphy, J. Kefer, and H. M. Wood, “Incidence and significance of prostatic stones in men with chronic prostatitis/chronic pelvic pain syndrome,” Urology, vol. 70, no. 2, pp. 235–238, 2007. View at: Publisher Site | Google Scholar
  48. P. Castro, C. Xia, L. Gomez, D. J. Lamb, and M. Ittmann, “Interleukin-8 expression is increased in senescent prostatic epithelial cells and promotes the development of benign prostatic hyperplasia,” Prostate, vol. 60, no. 2, pp. 153–159, 2004. View at: Publisher Site | Google Scholar
  49. D. Giri and M. Ittmann, “Interleukin-8 is a paracrine inducer of fibroblast growth factor 2, a stromal and epithelial growth factor in benign prostatic hyperplasia,” The American Journal of Pathology, vol. 159, no. 1, pp. 139–147, 2001. View at: Publisher Site | Google Scholar
  50. G. Penna, N. Mondaini, S. Amuchastegui et al., “Seminal plasma cytokines and chemokines in prostate inflammation: interleukin 8 as a predictive biomarker in chronic prostatitis/chronic pelvic pain syndrome and benign prostatic hyperplasia,” European Urology, vol. 51, no. 2, pp. 524–533, 2007. View at: Publisher Site | Google Scholar
  51. K. Fujita, C. M. Ewing, R. H. Getzenberg, J. K. Parsons, W. B. Isaacs, and C. P. Pavlovich, “Monocyte chemotactic protein-1 (MCP-1/CCL2) is associated with prostatic growth dysregulation and benign prostatic hyperplasia,” The Prostate, vol. 70, no. 5, pp. n/a–481, 2010. View at: Publisher Site | Google Scholar
  52. A. Latil, C. Libon, M. Templier, D. Junquero, F. Lantoine-Adam, and T. Nguyen, “Hexanic lipidosterolic extract of Serenoa repens inhibits the expression of two key inflammatory mediators, MCP-1/CCL2 and VCAM-1, in vitro,” BJU International, vol. 110, no. 6b, pp. E301–E307, 2012. View at: Publisher Site | Google Scholar
  53. D. V. Kouiavskaia, S. Southwood, C. A. Berard, E. N. Klyushnenkova, and R. B. Alexander, “T-cell recognition of prostatic peptides in men with chronic prostatitis/chronic pelvic pain syndrome,” The Journal of Urology, vol. 182, no. 5, pp. 2483–2489, 2009. View at: Publisher Site | Google Scholar
  54. G. Penna, S. Amuchastegui, C. Cossetti et al., “Spontaneous and prostatic steroid binding protein peptide-induced autoimmune prostatitis in the nonobese diabetic mouse,” Journal of Immunology, vol. 179, no. 3, pp. 1559–1567, 2007. View at: Publisher Site | Google Scholar
  55. S. Ponniah, I. Arah, and R. B. Alexander, “PSA is a candidate self-antigen in autoimmune chronic prostatitis/chronic pelvic pain syndrome,” The Prostate, vol. 44, no. 1, pp. 49–54, 2000. View at: Publisher Site | Google Scholar
  56. R. S. Matulewicz, A. B. Weiner, and E. M. Schaeffer, “Active surveillance for prostate cancer,” JAMA, vol. 318, no. 21, p. 2152, 2017. View at: Publisher Site | Google Scholar
  57. F. J. Grant, D. A. Taylor, P. O. Sheppard et al., “Molecular cloning and characterization of a novel transglutaminase cDNA from a human prostate cDNA library,” Biochemical and Biophysical Research Communications, vol. 203, no. 2, pp. 1117–1123, 1994. View at: Publisher Site | Google Scholar
  58. H. G. Williams-Ashman, “Transglutaminases and the clotting of mammalian seminal fluids,” Molecular and Cellular Biochemistry, vol. 58, no. 1-2, pp. 51–61, 1984. View at: Publisher Site | Google Scholar
  59. M. A. Cukierski, J. L. Sina, S. Prahalada, and R. T. Robertson, “Effects of seminal vesicle and coagulating gland ablation on fertility in rats,” Reproductive Toxicology, vol. 5, no. 4, pp. 347–352, 1991. View at: Publisher Site | Google Scholar
  60. D. C. Mukherjee, A. K. Agrawal, R. Manjunath, and A. B. Mukherjee, “Suppression of epididymal sperm antigenicity in the rabbit by uteroglobin and transglutaminase in vitro,” Science, vol. 219, no. 4587, pp. 989–991, 1983. View at: Publisher Site | Google Scholar
  61. G. Paonessa, S. Metafora, G. Tajana et al., “Transglutaminase-mediated modifications of the rat sperm surface in vitro,” Science, vol. 226, no. 4676, pp. 852–855, 1984. View at: Publisher Site | Google Scholar
  62. A. Peter, H. Lilja, Å. Lundwall, and J. Malm, “Semenogelin I and semenogelin II, the major gel-forming proteins in human semen, are substrates for transglutaminase,” European Journal of Biochemistry, vol. 252, no. 2, pp. 216–221, 1998. View at: Publisher Site | Google Scholar
  63. J. C. Romijn, “Polyamines and transglutaminase actions: Polyamine und Transglutaminase-Wirkungen,” Andrologia, vol. 22, Supplement 1, pp. 83–91, 1990. View at: Publisher Site | Google Scholar
  64. N. Landegren, D. Sharon, A. K. Shum et al., “Transglutaminase 4 as a prostate autoantigen in male subfertility,” Science Translational Medicine, vol. 7, no. 292, article 292ra101, 2015. View at: Publisher Site | Google Scholar
  65. S. E. Iismaa, “The prostate-specific protein, transglutaminase 4 (TG4), is an autoantigen associated with male subfertility,” Annals of Translational Medicine, vol. 4, article S35, Supplement 1, 2016. View at: Publisher Site | Google Scholar
  66. H. J. Dubbink, N. S. Verkaik, P. W. Faber, J. Trapman, F. H. Schröder, and J. C. Romijn, “Tissue specific and androgen-regulated expression of human prostate-specific transglutaminase,” Biochemical Journal, vol. 315, no. 3, pp. 901–908, 1996. View at: Publisher Site | Google Scholar
  67. H. J. Dubbink, R. F. Hoedemaeker, T. Van der Kwast, F. Schröder, and J. C. Romijn, “Human prostate-specific transglutaminase: a new prostatic marker with a unique distribution pattern,” Laboratory Investigation, vol. 79, no. 2, pp. 141–150, 1999. View at: Google Scholar
  68. G. C. Rivera-Gonzalez, A. P. Droop, H. J. Rippon et al., “Retinoic acid and androgen receptors combine to achieve tissue specific control of human prostatic transglutaminase expression: a novel regulatory network with broader significance,” Nucleic Acids Research, vol. 40, no. 11, pp. 4825–4840, 2012. View at: Publisher Site | Google Scholar
  69. H. J. Dubbink, L. de Waal, R. van Haperen, N. S. Verkaik, J. Trapman, and J. C. Romijn, “The human prostate-specific transglutaminase gene (TGM4): genomic organization, tissue-specific expression, and promoter characterization,” Genomics, vol. 51, no. 3, pp. 434–444, 1998. View at: Publisher Site | Google Scholar
  70. G. An, C. S. R. Meka, S. P. Bright, and R. W. Veltri, “Human prostate-specific transglutaminase gene: promoter cloning, tissue-specific expression, and down-regulation in metastatic prostate cancer,” Urology, vol. 54, no. 6, pp. 1105–1111, 1999. View at: Publisher Site | Google Scholar
  71. G. Davies, R. J. Ablin, M. D. Mason, and W. G. Jiang, “Expression of the prostate transglutaminase (TGase-4) in prostate cancer cells and its impact on the invasiveness of prostate cancer,” Journal of Experimental Therapeutics & Oncology, vol. 6, no. 3, pp. 257–264, 2007. View at: Google Scholar
  72. J. L. Thielen, K. G. Volzing, L. S. Collier, L. E. Green, D. A. Largaespada, and P. C. Marker, “Markers of prostate region-specific epithelial identity define anatomical locations in the mouse prostate that are molecularly similar to human prostate cancers,” Differentiation, vol. 75, no. 1, pp. 49–61, 2007. View at: Publisher Site | Google Scholar
  73. W. G. Jiang, R. J. Ablin, H. G. Kynaston, and M. D. Mason, “The prostate transglutaminase (TGase-4, TGaseP) regulates the interaction of prostate cancer and vascular endothelial cells, a potential role for the ROCK pathway,” Microvascular Research, vol. 77, no. 2, pp. 150–157, 2009. View at: Publisher Site | Google Scholar
  74. B. J. Blencowe, “Alternative splicing: new insights from global analyses,” Cell, vol. 126, no. 1, pp. 37–47, 2006. View at: Publisher Site | Google Scholar
  75. M. J. Pajares, T. Ezponda, R. Catena, A. Calvo, R. Pio, and L. M. Montuenga, “Alternative splicing: an emerging topic in molecular and clinical oncology,” The Lancet Oncology, vol. 8, no. 4, pp. 349–357, 2007. View at: Publisher Site | Google Scholar
  76. Z. Shaikhibrahim, A. Lindstrot, R. Buettner, and N. Wernert, “Analysis of laser-microdissected prostate cancer tissues reveals potential tumor markers,” International Journal of Molecular Medicine, vol. 28, no. 4, pp. 605–611, 2011. View at: Publisher Site | Google Scholar
  77. S. Principe, Y. Kim, S. Fontana et al., “Identification of prostate-enriched proteins by in-depth proteomic analyses of expressed prostatic secretions in urine,” Journal of Proteome Research, vol. 11, no. 4, pp. 2386–2396, 2012. View at: Publisher Site | Google Scholar
  78. Y. Kim, V. Ignatchenko, C. Q. Yao et al., “Identification of differentially expressed proteins in direct expressed prostatic secretions of men with organ-confined versus extracapsular prostate cancer,” Molecular & Cellular Proteomics, vol. 11, no. 12, pp. 1870–1884, 2012. View at: Publisher Site | Google Scholar
  79. R. J. Ablin, S. Owen, and W. G. Jiang, “Prostate transglutaminase (TGase-4) induces epithelial-to-mesenchymal transition in prostate cancer cells,” Anticancer Research, vol. 37, no. 2, pp. 481–488, 2017. View at: Publisher Site | Google Scholar
  80. S. Kumar and K. Mehta, “Tissue transglutaminase, inflammation, and cancer: how intimate is the relationship?” Amino Acids, vol. 44, no. 1, pp. 81–88, 2013. View at: Publisher Site | Google Scholar
  81. B. Friedrichs, H. Riedmiller, H. W. Goebel, U. Rausch, and G. Aumüller, “Immunological characterization and activity of transglutaminases in human normal and malignant prostate and in prostate cancer cell lines,” Urological Research, vol. 23, no. 5, pp. 301–310, 1995. View at: Publisher Site | Google Scholar
  82. S. Chen, F. Lin, S. Iismaa, K. N. Lee, P. J. Birckbichler, and R. M. Graham, “α1-adrenergic receptor signaling via gh is subtype specific and independent of its transglutaminase activity,” Journal of Biological Chemistry, vol. 271, no. 50, pp. 32385–32391, 1996. View at: Publisher Site | Google Scholar
  83. N. Suto, K. Ikura, and R. Sasaki, “Expression induced by interleukin-6 of tissue-type transglutaminase in human hepatoblastoma HepG2 cells,” Journal of Biological Chemistry, vol. 268, no. 10, pp. 7469–7473, 1993. View at: Google Scholar
  84. G. S. Kuncio, M. Tsyganskaya, J. Zhu et al., “TNF-α modulates expression of the tissue transglutaminase gene in liver cells,” American Journal of Physiology-Gastrointestinal and Liver Physiology, vol. 274, no. 2, pp. G240–G245, 1998. View at: Publisher Site | Google Scholar
  85. G. Quan, J. Y. Choi, D. S. Lee, and S. C. Lee, “TGF-β1 up-regulates transglutaminase two and fibronectin in dermal fibroblasts: a possible mechanism for the stabilization of tissue inflammation,” Archives of Dermatological Research, vol. 297, no. 2, pp. 84–90, 2005. View at: Publisher Site | Google Scholar
  86. A. P. Mann, A. Verma, G. Sethi et al., “Overexpression of tissue transglutaminase leads to constitutive activation of nuclear factor-κB in cancer cells: delineation of a novel pathway,” Cancer Research, vol. 66, no. 17, pp. 8788–8795, 2006. View at: Publisher Site | Google Scholar
  87. S. S. Park, J. M. Kim, D. S. Kim, I. H. Kim, and S. Y. Kim, “Transglutaminase 2 mediates polymer formation of I-κBα through C-terminal glutamine cluster,” Journal of Biological Chemistry, vol. 281, no. 46, pp. 34965–34972, 2006. View at: Publisher Site | Google Scholar
  88. K. S. Park, D. S. Kim, C. Ko, S.-J. Lee, S. H. Oh, and S.-Y. Kim, “TNF-α mediated NF-kappaB activation is constantly extended by transglutaminase 2,” Frontiers in Bioscience, vol. E3, pp. 341–354, 2011. View at: Publisher Site | Google Scholar
  89. M. Cummings, “Apoptosis of epithelial cells in vivo involves tissue transglutaminase upregulation,” The Journal of Pathology, vol. 179, no. 3, pp. 288–293, 1996. View at: Publisher Site | Google Scholar
  90. R. S. Rittmaster, R. W. Norman, L. N. Thomas, and G. Rowden, “Evidence for atrophy and apoptosis in the prostates of men given finasteride,” The Journal of Clinical Endocrinology & Metabolism, vol. 81, no. 2, pp. 814–819, 1996. View at: Publisher Site | Google Scholar
  91. O. J. Hickman, P. Dasgupta, C. Galustian, R. A. Smith, and A. Vyakarnam, “Cathepsin-L and transglutaminase dependent processing of ps20: a novel mechanism for ps20 regulation via ECM cross-linking,” Biochemistry and Biophysics Reports, vol. 7, pp. 328–337, 2016. View at: Publisher Site | Google Scholar
  92. R. L. Eckert, M. L. Fisher, D. Grun, G. Adhikary, W. Xu, and C. Kerr, “Transglutaminase is a tumor cell and cancer stem cell survival factor,” Molecular Carcinogenesis, vol. 54, no. 10, pp. 947–958, 2015. View at: Publisher Site | Google Scholar
  93. P. J. Birckbichler, R. B. Bonner, R. E. Hurst, B. L. Bane, J. V. Pitha, and G. P. Hemstreet, “Loss of tissue transglutaminase as a biomarker for prostate adenocarcinoma,” Cancer, vol. 89, no. 2, pp. 412–423, 2000. View at: Publisher Site | Google Scholar
  94. B. J. Feldman and D. Feldman, “The development of androgen-independent prostate cancer,” Nature Reviews Cancer, vol. 1, no. 1, pp. 34–45, 2001. View at: Publisher Site | Google Scholar
  95. U. Jariwala, J. P. Cogan, L. Jia, B. Frenkel, and G. A. Coetzee, “Inhibition of AR-mediated transcription by binding of Oct1 to a motif enriched in AR-occupied regions,” Prostate, vol. 69, no. 4, pp. 392–400, 2009. View at: Publisher Site | Google Scholar
  96. V. M. Phatak, S. M. Croft, S. G. Rameshaiah Setty et al., “Expression of transglutaminase-2 isoforms in normal human tissues and cancer cell lines: dysregulation of alternative splicing in cancer,” Amino Acids, vol. 44, no. 1, pp. 33–44, 2013. View at: Publisher Site | Google Scholar
  97. T. S. Lai and C. S. Greenberg, “TGM2 and implications for human disease: role of alternative splicing,” Frontiers in Bioscience, vol. 18, no. 2, pp. 504–519, 2013. View at: Publisher Site | Google Scholar
  98. P. Torricelli, M. Caraglia, A. Abbruzzese, and S. Beninati, “γ-Tocopherol inhibits human prostate cancer cell proliferation by up-regulation of transglutaminase 2 and down-regulation of cyclins,” Amino Acids, vol. 44, no. 1, pp. 45–51, 2013. View at: Publisher Site | Google Scholar
  99. S. Martucciello, G. Paolella, C. Esposito, M. Lepretti, and I. Caputo, “Anti-type 2 transglutaminase antibodies as modulators of type 2 transglutaminase functions: a possible pathological role in celiac disease,” Cellular and Molecular Life Sciences, vol. 75, no. 22, pp. 4107–4124, 2018. View at: Publisher Site | Google Scholar

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