Canadian Journal of Gastroenterology and Hepatology

Canadian Journal of Gastroenterology and Hepatology / 2018 / Article
Special Issue

Hepatocellular Carcinoma: From Molecular Basis to Novel Treatment Approaches

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Review Article | Open Access

Volume 2018 |Article ID 7568742 |

Peyda Korhan, Yeliz Yılmaz, Ezgi Bağırsakçı, Ayşim Güneş, Hande Topel, Brian I. Carr, Neşe Atabey, "Pleiotropic Effects of Heparins: From Clinical Applications to Molecular Mechanisms in Hepatocellular Carcinoma", Canadian Journal of Gastroenterology and Hepatology, vol. 2018, Article ID 7568742, 8 pages, 2018.

Pleiotropic Effects of Heparins: From Clinical Applications to Molecular Mechanisms in Hepatocellular Carcinoma

Academic Editor: Pierluigi Toniutto
Received29 Jul 2018
Revised04 Oct 2018
Accepted09 Oct 2018
Published22 Oct 2018


Hepatocellular carcinoma (HCC) is a major health problem worldwide and most cases are incurable because of late presentation. It is the most common primary neoplasm of the liver and often arises in the context of a chronic liver disease that impairs coagulation. Portal vein thrombosis (PVT) is a common complication of HCC that is associated with a poor prognosis. Heparin derivatives are widely used in the management of venous thromboembolism (VTE). Among them low molecular weight heparin (LMWH) favorably influences the survival in patients with advanced cancer, including HCC. Due to their pleiotropic function, heparins affect tumorigenesis in many ways and may promote or hamper tumorigenic transformation depending on the cancer type and cancer stage along with their structural properties and concentration. Thus, their application as an antithrombotic along with the conventional therapy regime should be carefully planned to develop the best management strategies. In this review, we first will briefly review clinical applications of heparin derivatives in the management of cancer with a particular focus on HCC. We then summarize the state of knowledge whereby heparin can crosstalk with molecules playing a role in hepatocarcinogenesis. Lastly, we highlight new experimental and clinical research conducted with the aim of moving towards personalized therapy in cancer patients at risk of thromboembolism.

1. Introduction

Worldwide, liver cancer is the sixth most common cancer and is the second leading global cause of cancer-related deaths [1, 2]. Among all primary liver cancers, HCC is the most prevalent malignancy, accounting for approximately 90% of cases [13]. The prognosis for HCC is very poor, with an incidence rate almost equaling the mortality rate (overall ratio of mortality to incidence of 0.95) [1]. The incidence of HCC increases progressively worldwide with advancing age in all populations, reaching a peak at 70 years [1]. The highest incidence and mortality rates of HCC are found in the less developed regions of the world, such as Southeast Asian countries [1], as compared to those in more developed regions in Europe and North America [13]. This global variation in incidence rates of HCC is closely related to the risk factors for HCC. HCC is common in patients with advanced hepatic fibrosis and cirrhosis, particularly with chronic damage caused by HBV or HCV infection, alcohol abuse, metabolic disease, and nonalcoholic fatty liver disease/obesity [4]. Tobacco smoke inhalation and dietary ingestion of fungal aflatoxins have been also recognized as major risk factors for HCC [4]. HCC originates as a result of an accumulation of genetic and epigenetic alterations, leading to an aberrant production of driver molecules. These altered expression profiles result in a multistep progression of precursor lesions to invasive/advanced HCC [4]. Importantly, Cancer Research, UK, has announced that 49% of liver cancer cases in the UK are preventable [5]. HBV vaccination, the establishment of treatments for HBV or HCV infections and widespread screening for hepatitis B or C viral infection, and interrupting the transmission of hepatitis virus infection via blood transfusion and blood products have all been shown to prevent liver cancer in high-incidence countries such as Japan [1, 5, 6].

Advances in science and technology have resulted in substantial opportunities for the management of HCC; however, prognosis of this disease is still poor due to the advanced stage at disease presentation, often due to absence of pathognomonic symptoms [710]. Larger tumor size, vascular invasion, poor liver functional status, and nodal metastasis are all associated with a poor prognosis [710]. Additionally, extraordinary inter- and intratumor heterogeneity of HCC contribute to drug resistance and recurrence, which pose a substantial bar to survival [11].

This complexity of HCC has led to the development of staging systems which combine both tumor and liver factors and a set of management guidelines, such as the Barcelona Clinic Liver Cancer (BCLC) guidelines recommended by the American Association for the Study of Liver Diseases (AASLD) and the European Association for the Study of the Liver (EASL) [810]. Surgical resection, transplantation, and ablation are potentially curative treatment options for HCC [810]. Unfortunately, less than 30% of patients globally who are diagnosed with early stage disease (Stage 0 or A) are eligible for these procedures [810]. For patients with intermediate stage disease (stage B), where patients are not eligible to be operated on, transarterial chemoembolisation (TACE) or transarterial radioembolisation (TARE) are recommended to establish local control and palliation [810]. TACE could potentially also be an adjuvant therapy for resectable HCC patients after hepatectomy, which could prevent recurrence and improve long-term survival [810]. Patients with advanced HCC which is considered as incurable have limited treatment options and chemotherapy provides minimal clinical benefit. Currently, Sorafenib, Lenvatinib, Regorafenib, or Opdivo, which are multitargeted kinase inhibitors or immune checkpoint inhibitors (Opdivo), are the only systemic agents demonstrated to extend overall survival (OS) compared with placebo in patients with advanced HCC by approximately three months [1214].

Although TACE is relatively safe, it may cause liver damage complications, especially in presence of PVT [15]. In addition, like many cancers, HCC is also associated with hemostatic activation, with a reported incidence of PVT ranging from 20%-65% [16]. The presence of PVT in patients with HCC is associated with systemic VTE, worse hepatic function, intraarterial tumor invasion, portal hypertension, and poorer tolerance to undergoing treatment which are collectively lead to reduced survival [16, 17]. Not surprisingly, PVT is frequent in patients with liver cirrhosis which can be life-threatening [18]. Hemostatic alterations are well documented in liver disease: hemostasis is often impaired by thrombocytopenia and the reduced synthesis of coagulation factors that normally takes places in the liver [19]. These alterations can be worsened following surgery and chemotherapy even causing hemorrhagic complications [20, 21]. Thus, pharmacological prophylaxis of VTE is often needed in HCC patients. Despite the clinical relevance of the matter, there are no guidelines available on the administration of anti-thromboembolic prophylaxis in HCC patients. Currently, LMWH is strongly recommended for intervention in the prevention and management of thromboembolism complications [2123]. Strikingly, several clinical and experimental studies have suggested that heparin derivatives affect cancer progression independent of their anticoagulant effects. Considering the fact that heparin derivatives are involved in a wide variety of biological activities, their application as an antithrombotic along with conventional therapy regime should be carefully planned to develop the best management strategies.

In this review, we firstly briefly review clinical applications of heparin derivatives in the management of cancer with a particular focus on HCC. Then we summarize the state of knowledge whereby heparin can cross-talk with molecules playing a role in hepatocarcinogenesis. Lastly, we highlight new experimental and clinical research conducted with the aim of moving towards personalized therapy in cancer patient at risk of thromboembolism.

2. Heparin Derivatives in the Management of Cancer

As mentioned above, patients with cancer are frequently treated with anti-coagulants, such as heparins, to treat or prevent thrombosis. Heparins are not absorbed orally, thus, they must be administrated parentally by intravenous infusion or subcutaneous injections [24]. UFH and other LMWHs, such as fondaparinux and danaparoid, do not possess intrinsic anticoagulant activity but potentiate antithrombin III that inhibits activated coagulation agents [25]. For many years unfractionated heparin (UFH) has been the standard treatment for initial anticoagulation [26]. However, recent randomized trials have demonstrated that LMWH is possibly superior to UFH in the initial treatment of VTE in people with cancer [26]. Moreover, LMWH provide other advantages versus UFH, including lower cost and simple dosing, and is associated with a lower risk for heparin-induced thrombocytopenia (HIT) [27]. Thus, LMWH is strongly recommended for intervention in the prevention and management of thromboembolism complications in cancer [2123]. However, long-term use has been associated with bruising at injection sites, recurrent thromboembolism, thrombocytopenia, and bleeding which then causes interruption of essential cancer therapies [22, 26].

Importantly, randomized trials comparing LMWH to UFH for the treatment of thrombosis have also indicated that heparins may improve outcomes of patients with cancer, particularly in those with early stage disease cancer including HCC and in patients with small cell lung [28, 29]. The PROTECHT study (Prophylaxis of Thromboembolism during Chemotherapy; Identifier: NCT00951574) has been designed to evaluate if prophylaxis with nadroparin (LMWH) conferred any additional benefit in terms survival, depending on whether chemotherapy disease control was achieved [30]. Notably, a statistically significant interaction between nadroparin treatment and response to chemotherapy was found, thus supporting the hypothesis difference in survival depends on the response to chemotherapy and nadroparin [30]. LMWHs lend themselves to such studies because of their pleiotropic effects and the relative ease of administration compared to UFH. A completed clinical trial, the results of which have not yet been released, investigated whether addition of LMWHs to TACE would improve HCC patient compared with TACE alone ( Identifier: NCT00827554). In addition, a current trial, which is not recruiting yet, aims to examine antithrombotic therapy with TACE in HCC to minimize mortality and to improve survival rate without provoking excessive bleeding ( Identifier: NCT02715492).

3. Heparin Derivatives

Heparin is a glycosaminoglycan that is synthesized by mast cells and basophils. Glycosaminoglycans are linear carbohydrate polymers that are composed of alternating uronate and hexosamine saccharides linked by glyosidic linkages [31]. Heparin undergoes extensive sulfation and rarely phosphorylation or carboxylation during synthesis and hence is a highly negatively charged biological molecule [32]. UHF is a naturally occurring mixture of glycosaminoglycan chains from porcine or bovine origin, each consisting of 200-300 saccharides units with molecular weights in the range of 12-14 kDa [33, 34]. LMWH consists of smaller fragments of UFH (nearly 18 saccharide units long, molecular weight approximately 5 kDa) produced by controlled enzymatic or chemical depolymerisation [33, 34]. Due to their structural differences, LMWH have relatively little antithrombotic activity compared to UFH [32].

4. Brief Review for Mechanisms of Heparin Affects Cancer Pathways

There are multiple experimental studies supporting the hypothesis that cancer progression can be influenced by heparins. Several in vitro and in vivo cancer models supported the idea that cancer cells exploit the coagulation system to facilitate cell growth, angiogenesis, immune evasion, and metastasis formation, by distinct mechanisms. In addition, numerous studies have demonstrated that heparins do not affect cancer only by their interaction with the coagulation cascade but also by various other ways, including by inhibition of cell-cell interaction by blocking cell-adhesion molecules (selectins), the inhibition of extracellular matrix proteinase heparanase, and the inhibition of angiogenesis.

Heparins are located primarily in the cell membrane and the extracellular matrix (ECM). They bind transiently with ECM-associated molecules, like the growth factors, cytokines, and enzymes, and alter their organization and functions [35]. One such example is heparin involvement in vascular epithelial growth factor- (VEGF-) fibronectin binding, where transient interaction of heparin with fibronectin promotes an open-conformation of fibronectin, which enhances binding to VEGF [36]. Consequently, VEGF binding to fibronectin is sufficient to mediate VEGF induced Erk1/2 activation, endothelial cell proliferation, and migration which are key steps in angiogenesis [37]. Moreover, blockage of the interaction between heparin and fibroblast growth factor (FGF), a well-known stimulator of angiogenesis, inhibits angiogenesis, tumor growth, and metastasis [38]. Duckworth et al. have shown that chemically modified heparin inhibits galectin-3-ligand binding and thereby prevents cancer-cell-endothelial adhesion and angiogenesis [39]. Also, heparin enhances ECM remodeling through the activation of metalloproteinase-2 and acts as a heparanase inhibitor that results in in vitro tubular morphogenesis of microvessels that is necessary for angiogenesis [33, 40]. Similarly, chemically modified nonanticoagulant species of heparin that specifically inhibit selectin-mediated heparanase enzymatic activity attenuate metastasis of melanoma cells [41]. It has been reported that heparin binds to platelets via P-selectin and prevents tumor invasion in lung cancer cells [42] Borsig et al. reported that heparin blocks P-selectin based platelet interactions through cell surface proteins such as mucins and thereby attenuates metastasis [42]. Furthermore, heparin binds L- and P-selectins to inhibit acute inflammation and thereby suppresses inflammatory processes in tumor microenvironment which is important for immune evasion. Moreover, heparin can also inhibit fibrin deposition around tumor cells for protecting cells from the immune system [43].

Another heparin interacting protein is factor 4 (CXCL4-PF4) which is released from activated platelets during platelet aggregation and promotes blood coagulation [44]. In addition, CXCL4-PF4 induces immune cells activation, differentiation, and migration but also inhibits endothelial cell migration, proliferation, and angiogenesis [44]. Relevant for this review are the effects of CXCL4-PF4 on the hemostatic system [44]. CXCL4-PF4 and heparin binding neutralise heparin on the endothelial surface of blood vessels, thereby inhibiting local antithrombin III activity and promoting coagulation [44]. In some patients exposed to heparin, CXCL4-PF4/heparin complex triggers an immunogenic response eventually leading to production of anti-CXCL4-PF4/heparin antibodies [44]. This may lead to a severe clinical condition characterized by platelet activation and aggregation, thrombocytopenia, and thrombocytopenia, which is commonly called heparin-induced thrombocytopenia (HIT). HIT typically develops 5-14 days after exposure to prophylactic or therapeutic doses of heparin [45]. In some cases, patients who previously had been exposed to heparin trigger HIT quicker [45].

In contrast to the anticarcinogenic effect above, heparin may also be involved in the activation of the metastatic cascade by forming a complex with midkine (MK). MK is highly expressed in HCC and in cancers of the stomach, colon, esophagus, pancreas lung, neuroblastoma, glioma, and urinary bladder [4648]. MK is activated when it forms homodimers that are stabilised by heparin. Activated MK/heparin complex leads to metastasis and drug resistance [49]. Notably, Jia et al. demonstrated that LMWH significantly blocked coadhesion between connective tissue growth factor/CCN family 2 (CCN2) and low-density lipoprotein receptor-related protein 6 (LRP6) and enhanced chemotherapeutic effect of oxaliplatin on HCC [50]. CCN2 functions to orchestrate LRP6 which is coreceptor in Wnt signalling. Wnt signalling is key signaling related to stem-ness, and chemoresistance [50]. Combination treatment with oxaliplatin and LMWH showed improved response rates to chemotherapy [50] Likewise, Pfankuchen et al. reported that a therapeutic dosage of LMWH (tinzaparin) reversed cisplatin resistance in a clone of ovarian cancer cell line to the level of sensitive cells [51, 52]. According to the follow up study, cisplatin resistant cells showed 3-fold higher Wnt signaling activity compared to wild type cells and Wnt pathway blockade increased cisplatin sensitivity. LMWH treatment reduced Wnt pathway activity and TCF-4 expression and enhanced cisplatin sensitivity in cisplatin resistant clones [51].

LMWH is also used as a nanocarrier to deliver drugs in cancer therapies. Modification of heparin molecules to generate nanocarriers become useful for applications like imaging, disease, and cancer treatments. Yan et al. prepared gambogic acid grafted low molecular weight heparin micelles to combine anti-tumor effect of gambogic acid with anti-angiogenic and anti-metastatic effect of heparin [53]. This in vivo study suggested that drugs grafted to LMWHs can be delivered to the liver and enhance their therapeutic effects by combining antitumor effects of heparin [53]. Furthermore, Du et al. modified LMWH to carry doxorubicin to overcome doxorubicin resistance in HCC [54].

5. Factors Influencing the Pleiotropic Role of Heparins

Due to their heterogeneity and natural location, heparins are able to interact with a wide variety molecules and mediate diverse biological processes (Figure 1). Therefore, it is not surprising that the role of heparins in tumor genesis is context dependent.

To clarify the various potential mechanisms of heparin anticancer activity, Niers et al. evaluated the data from preclinical studies (published between 1960 and 2005) in which heparins have been tested as anticancer therapy [32]. They suggested that heparin may affect the formation of metastasis rather than the growth of primary tumors. They also documented that chemically modified heparins with no or limited anticoagulant activity also showed antimetastatic properties [32]. They concluded with possible mechanisms to explain the effects on the process of metastasis include inhibition of blood coagulation, inhibition of cancer cell-platelet, and cancer cell-endothelial interactions by inhibition of cell invasion and angiogenesis [32]. They also documented interesting results highlighting the importance of types, duration, timing, and dose of heparin used, animal tumor model tested, and route of heparin administration in the course of disease [32]. Similarly, LMWH treatment was shown to inhibit FGF-induced mitogenesis of tumor derived endothelial cells in a time and concentration dependent manner [55]. Likewise, in Jha et al.’s study, to understand the effects of molecular weight and concentration of heparin on transforming growth factor (TGF)-β1 signaling, they used heparin-containing hyaluronic acid based hydrogels to analyze growth factor affinity and retention [56]. At equal concentrations, high molecular weight heparin has the highest amount of TGF-β1 retention from hydrogel compared to low molecular weight or unfractionated heparin. This response is critical for stem cell differentiation and lineage specification [56]. LaRochelle et al. determined that low concentrations of heparin enhance the binding of keratinocyte growth factor (KGF) to its receptor in CHO cells lacking HS proteoglycans but this effect is not observed in wild type CHO cells. In contrast higher heparin concentrations inhibit KGF signaling [57]. Furthermore, while heparins with short chain lengths are not able to activate anaplastic lymphoma kinase (ALK), heparins with longer chain lengths can induce dimerization and activation ALK in neuroblastoma cells [58]. Interestingly, in our previous studies, we showed that heparin can activate the c-Met signaling pathway by activating dimerization of c-Met receptor, which can then induce HCC cell invasion [59] However, when Hepatocyte Growth Factor (HGF), ligand of c-Met, is in the environment, heparin suppressed HGF/c-Met signaling mediated adhesion, motility, and invasion [59]. When we performed a microarray analysis to identify the molecular mechanisms behind heparin mediated biological responses, we observed that heparin modulates transcription of several genes involved in glucose metabolism, tumor angiogenesis, and EMT [60]. In our further analysis, we demonstrated that heparin controlled thioredoxin-interacting protein (TXNIP) gene expression through two mechanisms: (1) it can either directly bind to a unique carbohydrate response element located on the promoter of this gene or (2) it can trigger epigenetic modifications [60]. In either case, increased expression of TXNIP, which is a regulator glucose metabolism, accelerates migration and invasion abilities of HCC cells [60]. These data imply that, in addition to its regulatory role on receptor dimerization and ligand binding to its receptor, heparin also has a transcription regulatory role in HCC.

Overall, these studies emphasised that both intrinsic (such as tumor type) and extrinsic (such as heparin type) determinants play roles in the actions of heparin on tumors. For instance, while heparin administration increases tumor growth and metastasis in colon cancer, it reduces metastases in fibrosarcomas, lung, prostate, and mammary carcinomas [6163]. These pleotropic effects of heparin might be related to expression or activation levels of growth factors and/or their receptors, as well as by heparin type and concentration. As summarized in Figure 2, heparin can directly bind to growth factor receptors or growth factors to stimulate signaling pathways, whereas it could block growth factor-receptor interaction as a context dependent manner.

6. Conclusions

The management of HCC along with other advanced-stage cancers remains a challenge. Venous thrombosis is a common complication in patients with cancer and indicates a poor prognosis. LMWH is widely used in the clinic as an anticoagulant as part of a treatment regimen in cancer patients to treat or control thrombosis. Many studies highlight the benefit of heparin derivatives in increasing patient survival, mostly through their antithrombotic effect. There is also a growing amount of evidence for the anticancer effects of heparin, which are mostly via its inhibition of metastasis rather than on primary tumor growth. However, there is also evidence revealing that heparin can act as a metastasis promoting agent. Clearly, due to its pleiotropic actions, heparin affects tumorigenesis in many ways and may promote or hamper cell transformation, depending on the cancer type and stage along with its structural properties and concentration. This phenomenon stresses the fact that heparin use in the clinic should be assessed carefully. In addition, the use of a same therapy approach for all patients might result in variable and unpredictable responses, because of heterogeneity among tumors and genotypic differences between patients. Hence, personalized medicine (PM) offers an attractive approach for cancer management and care. PM implements “-omic" sciences (genomics, epigenomics, transcriptomics, proteomics, etc.) to integrate various data sets with the aim of dissecting molecular signatures and functional pathways that help to classify tumor subtypes and determine their natural course, prognosis, and responsiveness to therapies [64]. Thus, stratification of the subset of patients who might respond to particular combinations of therapies is crucial in the management of cancer. For instance, mutations of the KDM6A, CUL9, FDG6, AKAp3, and RFN139 genes are associated with the development of PVT in advanced HBV-related HCC [65]. Since effective management of PVT may improve treatment results for HCC, these genes can be used for the identification or prediction of high-risk patients who will benefit most from antithrombotic therapy. Moreover, anti-CXCL4-PF4/heparin antibodies can be used as a predictive factor to identify patients who should avoid heparin treatment. Further studies are needed for better understanding of heparin and tumor biology and the determination of biomarkers for the planning of best evidence-based approaches that meet the needs of patients for disease treatment, reduction of symptoms, and improvement in quality of life.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this review.

Authors’ Contributions

Peyda Korhan and Yeliz Yılmaz have equal contributions.


  1. “GLOBOCAN 2012, Cancer Incidence and Mortality Worldwide: IARC, vol. 11, International Agency for Research on Cancer, Lyon, France, 2018”. View at: Google Scholar
  2. “Globocan 2012 Liver Cancer Act Sheet, IARC: International Agency Research on Cancer, Lyon, 2012”. View at: Google Scholar
  3. G. Klöppel and World Health Organization Classification of Tumours, Pathology and Genetics of Tumours of the Digestive System: Ductal Adenocarcinoma of the Pancreas, International Agency for Research on Cancer Press, 2000.
  4. J. M. Llovet, J. Zucman-Rossi, E. Pikarsky et al., “Hepatocellular carcinoma,” Nature Reviews Disease Primers, vol. 2, p. 16018, 2016. View at: Publisher Site | Google Scholar
  5. “Cancer Research UK Liver cancer risk factors,” 2014, View at: Google Scholar
  6. M. Ikeda, S. Mitsunaga, S. Shimizu, I. Ohno, H. Takahashi et al., “Current status of hepatocellular carcinoma in Japan,” Chinese Clinical Oncology, vol. 2, no. 4, p. 40, 2013. View at: Google Scholar
  7. European Association for the Study of The Liver, “EASL-EORTC Clinical Practice Guidelines: management of hepatocellular carcinoma,” European Journal of Cancer, vol. 48, no. 5, pp. 599–641, 2012. View at: Publisher Site | Google Scholar
  8. P. R. Galle, A. Forner, J. M. Llovet et al., “EASL Clinical Practice Guidelines: Management of hepatocellular carcinoma,” Journal of Hepatology, vol. 69, no. 1, pp. 182–236, 2018. View at: Publisher Site | Google Scholar
  9. J. W. Park, M. Chen, M. Colombo et al., “Global patterns of hepatocellular carcinoma management from diagnosis to death: the BRIDGE Study,” Liver International, vol. 35, no. 9, pp. 2155–2166, 2015. View at: Publisher Site | Google Scholar
  10. J. Bruix, M. Reig, and M. Sherman, “Evidence-based diagnosis, staging, and treatment of patients with hepatocellular carcinoma,” Gastroenterology, vol. 150, no. 4, pp. 835–853, 2016. View at: Publisher Site | Google Scholar
  11. L. Li and H. Wang, “Heterogeneity of liver cancer and personalized therapy,” Cancer Letters, vol. 379, no. 2, pp. 191–197, 2016. View at: Publisher Site | Google Scholar
  12. C. J. Wilhelm, R. A. Johnson, P. G. Lysko, A. J. Eshleman, and A. Janowsky, “Effects of methamphetamine and lobeline on vesicular monoamine and dopamine transporter-mediated dopamine release in a cotransfected model system,” The Journal of Pharmacology and Experimental Therapeutics, vol. 310, no. 3, pp. 1142–1151, 2004. View at: Publisher Site | Google Scholar
  13. J. M. Llovet, S. Ricci, V. Mazzaferro et al., “Sorafenib in advanced hepatocellular carcinoma,” The New England Journal of Medicine, vol. 359, no. 4, pp. 378–390, 2008. View at: Publisher Site | Google Scholar
  14. J. Bruix, S. Qin, P. Merle et al., “Regorafenib for patients with hepatocellular carcinoma who progressed on sorafenib treatment (RESORCE): a randomised, double-blind, placebo-controlled, phase 3 trial,” The Lancet, vol. 389, no. 10064, pp. 56–66, 2017. View at: Publisher Site | Google Scholar
  15. J. P. Silva, N. G. Berger, S. Tsai et al., “Transarterial chemoembolization in hepatocellular carcinoma with portal vein tumor thrombosis: a systematic review and meta-analysis,” HPB, vol. 19, no. 8, pp. 659–666, 2017. View at: Publisher Site | Google Scholar
  16. G. C. Connolly, R. Chen, O. Hyrien et al., “Incidence, risk factors and consequences of portal vein and systemic thromboses in hepatocellular carcinoma,” Thrombosis Research, vol. 122, no. 3, pp. 299–306, 2008. View at: Publisher Site | Google Scholar
  17. S. L. Chan, C. C. N. Chong, A. W. H. Chan, D. M. C. Poon, and K. S. H. Chok, “Management of hepatocellular carcinoma with portal vein tumor thrombosis: Review and update at 2016,” World Journal of Gastroenterology, vol. 22, no. 32, pp. 7289–7300, 2016. View at: Publisher Site | Google Scholar
  18. L. von Köckritz, A. De Gottardi, J. Trebicka, and M. Praktiknjo, “Portal vein thrombosis in patients with cirrhosis,” Gastroenterology Report, vol. 5, no. 2, pp. 148–156, 2017. View at: Publisher Site | Google Scholar
  19. T. Lisman and F. W. G. Leebeek, “Hemostatic alterations in liver disease: A review on pathophysiology, clinical consequences, and treatment,” Digestive Surgery, vol. 24, no. 4, pp. 250–258, 2007. View at: Publisher Site | Google Scholar
  20. M. Vivarelli, M. Zanello, C. Zanfi et al., “Prophylaxis for venous thromboembolism after resection of hepatocellular carcinoma on cirrhosis: Is it necessary?” World Journal of Gastroenterology, vol. 16, no. 17, pp. 2146–2150, 2010. View at: Publisher Site | Google Scholar
  21. O. Negm, S. Abou Saif, M. El Gharib, M. Yousef, and S. Abd-Elsalam, “Role of low-molecular-weight heparins in prevention of thromboembolic complication after transarterial chemoembolization in hepatocellular carcinoma,” European Journal of Gastroenterology & Hepatology, vol. 29, no. 3, pp. 317–321, 2017. View at: Publisher Site | Google Scholar
  22. S. Noble, A. Nelson, and S. Seaman, “Cancer-associated thrombosis, low-molecular-weight heparin, and the patient experience: a qualitative study,” Patient Preference and Adherence, vol. 8, pp. 453–461, 2014. View at: Google Scholar
  23. M. B. Hakoum, L. A. Kahale, I. G. Tsolakian et al., “Anticoagulation for the initial treatment of venous thromboembolism in people with cancer,” Cochrane Database of Systematic Reviews, 2018. View at: Google Scholar
  24. J. Hirsh, “Low molecular weight heparin,” Thrombosis and Haemostasis, vol. 70, no. 1, pp. 204–207, 1993. View at: Publisher Site | Google Scholar
  25. J. Hirsh, K. A. Bauer, and M. B. Donati, “Parenteral anticoagulants: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines (8th Edition),” CHEST, vol. 133, supplement 6, pp. 141S–159S, 2008. View at: Publisher Site | Google Scholar
  26. E. Donnellan and A. A. Khorana, “Cancer and venous thromboembolic disease: a review,” The Oncologist, vol. 22, no. 2, pp. 199–207, 2017. View at: Publisher Site | Google Scholar
  27. N. Martel, J. Lee, and P. S. Wells, “Risk for heparin-induced thrombocytopenia with unfractionated and low-molecular-weight heparin thromboprophylaxis: a meta-analysis,” Blood, vol. 106, no. 8, pp. 2710–2715, 2005. View at: Publisher Site | Google Scholar
  28. D. Sanford, A. Naidu, N. Alizadeh, and A. Lazo-Langner, “The effect of low molecular weight heparin on survival in cancer patients: An updated systematic review and meta-analysis of randomized trials,” Journal of Thrombosis and Haemostasis, vol. 12, no. 7, pp. 1076–1085, 2014. View at: Publisher Site | Google Scholar
  29. N. Zhang, W. Lou, F. Ji, L. Qiu, B. K. Tsang, and W. Di, “Low molecular weight heparin and cancer survival: clinical trials and experimental mechanisms,” Journal of Cancer Research and Clinical Oncology, vol. 142, no. 8, pp. 1807–1816, 2016. View at: Publisher Site | Google Scholar
  30. S. Barni, E. Bonizzoni, M. Verso et al., “To the editor: The effect of low-molecular-weight heparin in cancer patients: The mirror image of survival?” Blood, vol. 124, no. 1, pp. 155-156, 2014. View at: Publisher Site | Google Scholar
  31. S. Mohamed and D. Coombe, “Heparin Mimetics: Their Therapeutic Potential,” Pharmaceuticals, vol. 10, no. 4, p. 78, 2017. View at: Publisher Site | Google Scholar
  32. T. M. H. Niers, C. P. W. Klerk, M. DiNisio et al., “Mechanisms of heparin induced anti-cancer activity in experimental cancer models,” Critical Review in Oncology/Hematology, vol. 61, no. 3, pp. 195–207, 2007. View at: Publisher Site | Google Scholar
  33. S. M. Smorenburg and C. J. F. Van Noorden, “The complex effects of heparins on cancer progression and metastasis in experimental studies,” Pharmacological Reviews, vol. 53, no. 1, pp. 93–105, 2001. View at: Google Scholar
  34. S. A. Mousa, R. Linhardt, J. L. Francis, and A. Amirkhosravi, “Anti-metastatic effect of a non-anticoagulant low-molecular-weight heparin versus the standard low-molecular-weight heparin, enoxaparin,” Thrombosis and Haemostasis, vol. 96, no. 6, pp. 816–821, 2006. View at: Publisher Site | Google Scholar
  35. F. Peysselon and S. Ricard-Blum, “Heparin-protein interactions: From affinity and kinetics to biological roles. Application to an interaction network regulating angiogenesis,” Matrix Biology, vol. 35, pp. 73–81, 2014. View at: Publisher Site | Google Scholar
  36. M. Mitsi, K. Forsten-Williams, M. Gopalakrishnan, and M. A. Nugent, “A catalytic role of heparin within the extracellular matrix,” The Journal of Biological Chemistry, vol. 283, no. 50, pp. 34796–34807, 2008. View at: Publisher Site | Google Scholar
  37. E. S. Wijelath, S. Rahman, M. Namekata et al., “Heparin-II domain of fibronectin is a vascular endothelial growth factor-binding domain: Enhancement of VEGF biological activity by a singular growth factor/matrix protein synergism,” Circulation Research, vol. 99, no. 8, pp. 853–860, 2006. View at: Publisher Site | Google Scholar
  38. S. M. Plum, J. W. Holaday, A. Ruiz, J. W. Madsen, W. E. Fogler, and A. H. Fortier, “Administration of a liposomal FGF-2 peptide vaccine leads to abrogation of FGF-2-mediated angiogenesis and tumor development,” Vaccine, vol. 19, no. 9-10, pp. 1294–1303, 2000. View at: Publisher Site | Google Scholar
  39. C. A. Duckworth, S. E. Guimond, P. Sindrewicz et al., “Chemically modified, non-anticoagulant heparin derivatives are potent galectin-3 binding inhibitors and inhibit circulating galectin-3-promoted metastasis,” Oncotarget , vol. 6, no. 27, pp. 23671–23687, 2015. View at: Google Scholar
  40. L. Ling, S. K. Tan, T. H. Goh et al., “Targeting the heparin-binding domain of fibroblast growth factor receptor 1 as a potential cancer therapy,” Molecular Cancer, vol. 14, no. 1, article no. 136, 2015. View at: Publisher Site | Google Scholar
  41. N. Hostettler, A. Naggi, G. Torri et al., “P-selectin- and heparanase-dependent antimetastatic activity of non-anticoagulant heparins,” The FASEB Journal, vol. 21, no. 13, pp. 3562–3572, 2007. View at: Publisher Site | Google Scholar
  42. L. Borsig, R. Wong, J. Feramisco, D. R. Nadeau, N. M. Varki, and A. Varki, “Heparin and cancer revisited: mechanistic connections involving platelets, P-selectin, carcinoma mucins, and tumor metastasis,” Proceedings of the National Acadamy of Sciences of the United States of America, vol. 98, no. 6, pp. 3352–3357, 2001. View at: Publisher Site | Google Scholar
  43. H. Engelberg, “Actions of heparin that may affect the malignant process,” Cancer, vol. 85, no. 2, pp. 257–272, 1999. View at: Google Scholar
  44. P. M. Sandset, “CXCL4-platelet factor 4, heparin-induced thrombocytopenia and cancer,” Thrombosis Research, vol. 129, pp. S97–S100, 2012. View at: Publisher Site | Google Scholar
  45. N. Lubenow, R. Kempf, A. Eichner, P. Eichler, L. E. Carlsson, and A. Greinacher, “Heparin-induced thrombocytopenia: Temporal pattern of thrombocytopenia in relation to initial use or reexposure to heparin,” CHEST, vol. 122, no. 1, pp. 37–42, 2002. View at: Publisher Site | Google Scholar
  46. J. Yao, W.-Y. Li, and S.-G. Gao, “The advances of Midkine with peripheral invasion in pancreatic cancer,” American Journal of Cancer Research, vol. 5, no. 9, pp. 2912–2917, 2015. View at: Google Scholar
  47. Y. Xu, X. Qu, X. Zhang et al., “Midkine positively regulates the proliferation of human gastric cancer cells,” Cancer Letters, vol. 279, no. 2, pp. 137–144, 2009. View at: Publisher Site | Google Scholar
  48. B. Sun, C. Hu, Z. Yang et al., “Midkine promotes hepatocellular carcinoma metastasis by elevating anoikis resistance of circulating tumor cells,” Oncotarget , vol. 8, no. 20, pp. 32523–32535, 2017. View at: Google Scholar
  49. K. Kadomatsu, S. Kishida, and S. Tsubota, “The heparin-binding growth factor midkine: the biological activities and candidate receptors,” The Journal of Biochemistry, vol. 153, no. 6, pp. 511–521, 2013. View at: Publisher Site | Google Scholar
  50. Q. Jia, Y. Bu, Z. Wang et al., “Maintenance of stemness is associated with the interation of LRP6 and heparin-binding protein CCN2 autocrined by hepatocellular carcinoma,” Journal of Experimental & Clinical Cancer Research, vol. 36, no. 1, article 117, 2017. View at: Publisher Site | Google Scholar
  51. D. B. Pfankuchen, F. Baltes, T. Batool, J. Li, M. Schlesinger, and G. Bendas, “Heparin antagonizes cisplatin resistance of A2780 ovarian cancer cells by affecting the Wnt signaling pathway,” Oncotarget, vol. 8, no. 40, pp. 67553–67566, 2017. View at: Google Scholar
  52. D. B. Pfankuchen, D. P. Stölting, M. Schlesinger, H.-D. Royer, and G. Bendas, “Low molecular weight heparin tinzaparin antagonizes cisplatin resistance of ovarian cancer cells,” Biochemical Pharmacology, vol. 97, no. 2, pp. 147–157, 2015. View at: Publisher Site | Google Scholar
  53. X. Yan, Y. Yang, L. He, D. Peng, and D. Yin, “Gambogic acid grafted low molecular weight heparin micelles for targeted treatment in a hepatocellular carcinoma model with an enhanced anti-angiogenesis effect,” International Journal of Pharmaceutics, vol. 522, no. 1-2, pp. 110–118, 2017. View at: Publisher Site | Google Scholar
  54. H. Du, M. Liu, A. Yu, J. Ji, and G. Zhai, “Insight into the role of dual-ligand modification in low molecular weight heparin based nanocarrier for targeted delivery of doxorubicin,” International Journal of Pharmaceutics, vol. 523, no. 1, pp. 427–438, 2017. View at: Publisher Site | Google Scholar
  55. S. L. Smiley, D. O. Henry, and M. K. Wong, “The mechanism of low molecular weight heparin (LMWH) inhibition of tumor growth,” Journal of Clinical Oncology, vol. 24, supplement 18, pp. 13093–13093, 2006. View at: Google Scholar
  56. A. K. Jha, A. Mathur, F. L. Svedlund, J. Ye, Y. Yeghiazarians, and K. E. Healy, “Molecular weight and concentration of heparin in hyaluronic acid-based matrices modulates growth factor retention kinetics and stem cell fate,” Journal of Controlled Release, vol. 209, pp. 308–316, 2015. View at: Publisher Site | Google Scholar
  57. W. J. LaRochelle, K. Sakaguchi, N. Atabey et al., “Heparan sulfate proteoglycan modulates keratinocyte growth factor signaling through interaction with both ligand and receptor,” Biochemistry, vol. 38, no. 6, pp. 1765–1771, 1999. View at: Publisher Site | Google Scholar
  58. P. B. Murray, I. Lax, A. Reshetnyak et al., “Heparin is an activating ligand of the orphan receptor tyrosine kinase ALK,” Science Signaling, vol. 8, no. 360, pp. ra6–ra6, 2015. View at: Publisher Site | Google Scholar
  59. E. Ozen, A. Gozukizil, E. Erdal, A. Uren, D. P. Bottaro, and N. Atabey, “Heparin inhibits Hepatocyte growth factor induced motility and invasion of hepatocellular carcinoma cells through early growth response protein 1,” PLoS ONE, vol. 7, no. 8, article e42717, 2012. View at: Publisher Site | Google Scholar
  60. A. Gunes, E. Iscan, H. Topel et al., “Heparin treatment increases thioredoxin interacting protein expression in hepatocellular carcinoma cells,” The International Journal of Biochemistry & Cell Biology, vol. 65, pp. 169–181, 2015. View at: Publisher Site | Google Scholar
  61. C. Lim, H. Multhaupt, and J. R. Couchman, “Cell surface heparan sulfate proteoglycans control adhesion and invasion of breast carcinoma cells,” Molecular Cancer, vol. 14, no. 1, article no. 15, 2015. View at: Publisher Site | Google Scholar
  62. G.-X. Zhong, Y. Gong, C.-J. Yu et al., “Significantly inhibitory effects of low molecular weight heparin (Fraxiparine) on the motility of lung cancer cells and its related mechanism,” Tumor Biology, vol. 36, no. 6, pp. 4689–4697, 2015. View at: Publisher Site | Google Scholar
  63. A. Takeuchi, Y. Yamamoto, S. Munesue et al., “Low molecular weight heparin suppresses receptor for advanced glycation end products-mediated expression of malignant phenotype in human fibrosarcoma cells,” Cancer Science, vol. 104, no. 6, pp. 740–749, 2013. View at: Publisher Site | Google Scholar
  64. P. Korhan, R. Verkerk, and W. R Critchley, “Scientific rationale for integrative and personalised strategies for pancreatic ductal adenocarcinoma management,” Integrative Molecular Medicine, vol. 4, no. 5, pp. 1–32, 2017. View at: Publisher Site | Google Scholar
  65. J. Huang, Q. Deng, Q. Wang et al., “Exome sequencing of hepatitis B virus-associated hepatocellular carcinoma,” Nature Genetics, vol. 44, no. 10, pp. 1117–1121, 2012. View at: Publisher Site | Google Scholar

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