Abstract
Serum interleukin-8 (IL-8) and interferon-alpha (IFN-α) levels have been estimated from a total of 88 individuals of which 19 were disease-free healthy individuals, and 69 were patients with thyroid diseases: goitre (), autoimmune diseases (), and carcinomas (). Both IL-8 and IFN-α were significantly higher in all the patients as compared to healthy individuals. Serum IL-8 levels showed significant positive correlation with disease stage in thyroid cancer patients. Higher serum IL-8 levels were associated with advanced disease stage while no significant correlation was observed between serum IFN-α levels and any of the clinicopathological parameters. IL-8 and IFN-α significantly correlated with each other in anaplastic carcinoma patients. Finally concluding, monitoring the serum IL-8 and IFN-α levels can help differentiate patients with thyroid diseases from healthy individuals, and IL-8 seems to have a role in the pathogenesis of thyroid diseases and may represent a target for innovative diagnostic and therapeutic strategies.
1. Introduction
Although thyroid problems are among the most common medical conditions, because their symptoms often appear gradually, they are commonly misdiagnosed. The three most common thyroid problems are the underactive thyroid, the overactive thyroid, and thyroid nodules [1]. Based on these problems, the disorders of the thyroid gland include: goitre, autoimmune thyroid diseases, as well as thyroid carcinoma.
Thyroid cancer is the fastest growing and most common cancer of the total endocrine malignancies, accounting for 94.5% of the total new endocrine cancers and 65.9% of the deaths due to endocrine cancers. It is the endocrine tumor that bears the highest incidence with 33 550 new cases per year in the US [2]. The vast majority of patients with thyroid diseases are curable using present treatment modalities. However, accumulating evidences indicate that follicular cell-derived thyroid cancer constitutes a biological continuum progressing from the highly curable well-differentiated thyroid cancer to the universally fatal anaplastic thyroid cancer [3, 4]. An association between thyroid cancer and a history of several benign diseases has been observed in most studies [5, 6]. However, the molecular mechanisms underlying thyroid cancer progression remain ill-defined. So it is important to decipher these mechanisms, since poorly differentiated and anaplastic carcinomas account for the majority of thyroid cancer-related deaths.
Moreover, accumulated epidemiologic studies support that chronic inflammatory diseases are frequently associated with increased risk of cancers [7–9]. It is estimated that underlying infections and inflammatory responses are linked to 15–20% of all deaths from cancer worldwide [7]. There are many triggers of chronic inflammation that increase the risk of developing cancer. Such triggers include microbial infections, autoimmune diseases, and inflammatory conditions of unknown origin. The hallmarks of cancer-related inflammation include the presence of inflammatory cells and inflammatory mediators (e.g., chemokines, cytokines, and prostaglandins) in tumor tissues, tissue remodeling and angiogenesis similar to that seen in chronic inflammatory responses, and tissue repair. Indeed, inflammatory cells and mediators are present in the microenvironment of most, if not all, tumors, irrespective of the trigger for development [10]. Cytokine shedding by tumor cells into the local microenvironment is an important modulator of tumorigenesis [11]. Thus, the relationship between the immune system and cancer is complex, and cytokines, chemokines, and growth factors in the tumor environment play a key role in this interaction [12].
Cytokines are a category of signaling proteins and glycoproteins that, like hormones and neurotransmitters, are used extensively in cellular communication, which mediate and regulate immunity, inflammation, and hematopoiesis. Thus, cytokines are a group of polypeptides produced mainly by inflammatory cells, but also by nonimmune cells, and have a key role in triggering and coordinating inflammatory and immune reactions [13].
However, the relationships between cytokines and cancer are multiple and bidirectional. On one hand, cytokines may directly influence carcinogenesis and metastasis by modifying the tumor phenotype while, on the other hand during tumor progression, modifications of the cytokine expression in the tumor environment may be induced by the tumor cells [14]. Thus, a better understanding of the basis of molecular talk between tumor cells and the immune system would be helpful in developing immunotherapeutic approaches.
Interleukin-8 (IL-8) is one of the best-characterized members of C-X-C subfamily of the chemotactic cytokines [15, 16]. It is a proinflammatory cytokine produced by macrophages and other cell types such as epithelial cells. As it serves as a chemical signal that attracts neutrophils at the site of inflammation, it is also called “neutrophil chemotactic factor”. Interleukin (IL)-8 is produced by a wide variety of normal cells as well as tumor cell and its principal role is in the initiation and amplification of acute inflammatory reactions. IL-8 has also been implicated in chronic inflammatory processes and diseases with a chronic inflammatory component such as cancer. IL-8 has been shown to contribute to human cancer progression through its potential functions as a mitogenic, angiogenic, and mitogenic factor [17, 18]. Recent studies have demonstrated that IL-8 regulates tumor cell growth and metastasis in melanoma [19], carcinoma of breast [20], stomach [21], pancreas [22], and liver [22, 23]. Elevated serum level of IL-8 was found to be a prognostic marker in soft tissue sarcoma [24], B-cell chronic lymphocytic leukemia [25], primary gastrointestinal non-Hodgkin’s lymphoma [26], and malignant melanoma [27].
So, understanding the mechanisms of IL-8 expression can be helpful in designing potential therapeutic strategies of targeting IL-8 to control tumor growth and metastasis. On the other hand, according to current data, endocrine system is closely related to immune system, and interferons play an important role in this relationship. Interferons can inhibit cell proliferation or control apoptosis [28].
Interferon-alpha (IFN-α) is a small protein released by macrophages, lymphocytes, and tissue cells infected with a virus, it has pleiotropic properties and exerts a wide range of immunomodulatory activities [29]. It is predominantly characterized as an antiviral and antiproliferative agent which stimulates both macrophages and natural killer cells to elicit an antiviral response, and it is also active against tumors. Besides, a very important property of IFN-α is its ability to arrest the cell in the G1-G0 phase, which is what determines static effect of IFN-α on growth of many tumors [28]. Moreover, IFN-α is a potent activator of monocytic functions. But, since human monocytes are major producers of neutrophil chemotactic cytokine: IL-8, we have been tempted to study levels of both these cytokines (IL-8 and IFN-α) in sera of patients with thyroid disorders by ELISA. Moreover, it is much more convenient to quantitate serum levels of these cytokines than to evaluate their expression in tissue specimens as the former approach is noninvasive and reproducible. Furthermore, it does not require tumor tissue specimens.
So, the aim of this study was to explore the occurrence of interleukin-8 and interferon-alpha in sera of patients with various thyroid diseases (goiter, autoimmune disorders, and thyroid carcinoma) and to correlate the results with clinicopathological parameters in thyroid cancer patients.
2. Materials and Methods
Our study included a group of 88 individuals, out of which 69 were patients with thyroid disorders (goiter: , autoimmune thyroid diseases: , and thyroid carcinoma: ) and 19 were age-matched disease-free healthy individuals (Table 1). The mean age of healthy individuals included in the study was 30.57 years (range: 18–56 years). Goiter occurred in patients at an earlier age (mean age: 34.23 years, range: 18–58 years) while the occurrence of autoimmune thyroid disease (mean age: 42.81 years, range: 26–61 years; ) and thyroid carcinoma (mean age: 43.96 years, range: 18–78 years; ) was found in more elderly people. But as in the American Joint Committee on Cancer (AJCC) TNM staging system, the patients are staged on the basis of their age (<45/≥45 years), we have also grouped our patients into a younger (<45 years) and an older group (≥45 years) (Table 1).
Fasting blood samples were collected in the morning from disease-free healthy individuals and patients with thyroid diseases in vacuettes with gel for serum separation. All patients with thyroid disorders were never previously treated with chemotherapy, surgery, or radiotherapy at the time of blood collection. Moreover, none of these patients were ever before diagnosed with any other autoimmune disease, no one of them was taking immunosuppressive or immunomodulant drugs. Prior to pretherapeutic blood collection, written consent of the patients was taken. Serums were separated from all blood samples after centrifugation and were stored at −80°C until analysis. IL-8 and IFN-α were determined from the serum samples using commercially available enzyme immunoassay (EIA) kits from Immunotech (A Beckman Coulter Company, France) following the manufacturer’s instructions. The detailed clinical and histopathological characteristics of all patients were noted from the case files maintained at Gujarat Cancer and Research Institute (Table 2).
2.1. Statistical Analysis
The results were presented as mean ± standard error of mean (M ± S.E.). Mann-Whitney U test was performed to assess the differences in serum IL-8 and IFN-α levels between healthy individuals and patients with thyroid diseases. Receiver’s operating characteristic (ROC) curves were also constructed to determine the discriminating efficacy of IL-8 and IFN-α between healthy individuals and patients with thyroid diseases. P values <.05 were considered statistically significant. Also, in thyroid cancer patients, the association between IL-8 and IFN-α levels and clinicopathological parameters was analyzed by Mann-Whitney U test, and the spearman’s correlation was used to describe independent relationship between serum IL-8 and IFN-α levels.
3. Results and Discussion
Serum IL-8 and IFN-α levels were significantly elevated in all patients with thyroid disorders (goitre, autoimmune thyroid disorders, and thyroid carcinoma) as compared to healthy individuals. IL-8 and IFN-α levels in thyroid carcinoma patients with different histopathological subgroups and stages have also been compared to that of healthy individuals. Statistically significant higher levels of both these cytokines were found in patients with papillary and follicular carcinoma while, in medullary carcinoma patients, IFN-α and, in anaplastic carcinoma patients, IL-8 levels were found to be significantly increased as compared to healthy individuals. Early-stage thyroid carcinoma patients exhibited significant higher levels of IFN-α, but not of IL-8, while IL-8 and not IFN-α levels were found significantly elevated in advanced-stage thyroid carcinoma patients in comparison to healthy individuals (Tables 3 and 4).
ROC curve (Figure 1(a)) indicates that both IL-8 and IFN-α exhibited a good discriminatory efficacy between healthy individuals and total patients with thyroid diseases (IL-8: AUC-0.756; IFN-α: AUC-0.795). Moreover, the ROC curves for both the cytokines between healthy individuals and individual groups of patients, that is, goiter, autoimmune disease, and thyroid cancer, revealed that both IL-8 as well as IFN-α showed good sensitivity and specificity to discriminate between healthy individuals and patients having different thyroid diseases (goiter- IL-8: AUC-0.774, IFN-α: AUC-0.797; autoimmune thyroid disease- IL-8: AUC-0.711, IFN-α: AUC-0.755, and thyroid cancer- IL-8: AUC-0.767, IFN-α: AUC-0.813) (Figures 1(b)–1(d)). Only IL-8 could significantly discriminate between early- and advanced-stage thyroid cancer patients (Figure 1(e)).
(a) Healthy individuals and total patients with thyroid disease
(b) Healthy individuals and patients with goiter
(c) Healthy individuals and patients with autoimmune thyroid disease
(d) Healthy individuals and thyroid cancer patients
(e) Early stage and advanced stage thyroid carcinoma
Similar to the present study, Limkov et al. have demonstrated statistically significant differences in IL-8 levels thyroid disease patients and reference normal group [30]. Bossowski and Urban and Siddiqi et al. have also observed significantly elevated levels of IL-8 in patients with Graves’ disease and nodular goiter as compared to the respective healthy control groups [31, 32]. In contrast to these of studies, Krassas and colleagues found that IL-8 levels were not elevated in Graves’ disease, toxic nodular goiter and Hashimoto’s thyroiditis [33]. A study by Lee et al. has shown increased levels of cytokines including IL-8 and IL-10 in patients who frequently developed euthyroid sick syndromes followed by allogeneic bone marrow transplantation [34]. Antonelli et al. observed increased CXCL10 levels in autoimmune thyroiditis [35]. Also, they have demonstrated elevated circulating levels of CXCL10 and IFN-gamma in patients with Graves’ disease, particularly in those with Graves’ ophthalmopathy [36]. Increased IL-8 levels have also been observed in patients with other malignancies. In their study, Yi. Ren et al. also found that the level of serum IL-8 was markedly elevated in most patients with HCC as compared with healthy subjects [37]. In fact, elevated serum level of IL-8 was found to be a prognostic marker in soft tissue sarcoma [38], B-cell chronic lymphocytic leukemia [39], primary gastrointestinal non-Hodgkin’s lymphoma [40], and malignant melanoma [41]. So, high serum levels of both the cytokines in thyroid carcinoma patients may be caused by an excessive production in tumor cells and subsequent release into the circulation.
The incidence of patients with thyroid diseases having higher levels of IL-8 and IFN-α than those of healthy individuals has been shown in Figures 2(a)–2(c). The levels of IL-8 > 7.00 ng/ml (maximum level of IL-8 in healthy individuals) were found in 57.10% of patients with goitre, 56.30% patients having autoimmune diseases and in 62.50% thyroid carcinoma patients. While levels of IFN-α > 4.00 ng/ml (maximum level in healthy individuals) were observed in only 14.30% patients with goitre, 6.30% patients with autoimmune diseases and in 18.80% thyroid carcinoma patients.
(a)
(b)
(c)
The incidence of thyroid carcinoma patients having higher levels of IL-8 as compared to that of healthy individuals increased with the increase in disease stage. That is, 40% of early-stage thyroid carcinoma patients as compared to 82.40% advanced-stage thyroid carcinoma patients had higher IL-8 levels than the maximum range found in healthy individuals.
Association of the serum IL-8 and IFN-α levels with different clinicopathological parameters have been studied by Mann-Whitney U test. It revealed that elevated serum IL-8 levels were significantly associated with advanced-disease stage (Figure 3). In fact, serum IL-8 levels were significantly increased in patients with advanced stage compared to those with early-stage disease (445.12 ± 214.30 versus 101.56 ± 53.89; ).
Moreover, Spearman rank’s correlation analysis revealed significant positive relationships between IL-8 levels and disease stage (, ). IFN-α levels were not significantly associated nor did they exhibit any significant relationship with any of the clinicopathological parameters. Yi Ren et al. demonstrated that high serum IL-8 level correlated with large tumor volume and advanced tumor stage in patients with hepatocellular carcinoma [37]. Increased IL-8 expression has been found in various tumors and in some studies IL-8 serum and/or tissue levels correlate with tumor progression and metastasis [42–45]. So, this finding additionally supports the role of IL-8 in the progression of thyroid carcinoma.
The relative risk study indicated that 14/17 advanced-stage thyroid carcinoma patients and 6/15 early-stage thyroid carcinoma patients had elevated IL-8 levels (>7.00 pg/ml) (Figure 4), which indicates IL-8 as a risk factor in development of advanced-stage thyroid cancer.
4. Conclusion
Finally concluding, as both serum IL-8 and IFN-α levels were significantly higher, not only in thyroid cancer patients, but also in patients having goitre and autoimmune diseases, they can be used for differentiating such patients, having any disease of thyroid gland, from that of healthy individuals. Since such conditions often constitute prevalent pre-existing disease states in the pathogenesis of thyroid cancer, these results strongly suggest an association between IL-8 and IFN-α upregulation and development of thyroid carcinoma.
Moreover, IL-8 could efficiently discriminate between early- and advanced-stage disease. Also, the major findings demonstrate that IL-8 levels, were significantly positively related to the disease stage and the elevated IL-8 levels were predominantly associated with the advanced stage of the disease whereas IFN-α levels did not show any significant correlation or association with any of the histopathological parameters of thyroid carcinoma patients. Thus, IL-8 seems to have a role in thyroid cancer pathogenesis, and measurement of preoperative serum IL-8 levels might be more useful and feasible in the clinical setting to predict tumor stage where it may represent a putative target for innovative diagnostic and therapeutic strategies. However, further studies including more number of patients and evaluating the postoperative changes in serum IL-8 levels may provide additional predictive value on tumor recurrence and prognosis.
Acknowledgments
This paper was financially supported by the Directorate of Medical Education and Researches (DMER-Gujarat state) and Gujarat Cancer Society (GCS), and it was approved by the GCRI/GCS ethics committee.