The Expression of Transforming Growth Factor Beta-1 and Interleukin-6 on Human Prostate: Prostate Hyperplasia and Prostate Cancer

Authors

  • Afdal Afdal Postgraduate Biomedical Science, Faculty of Medicine, Andalas University, Padang, Indonesia
  • Eryati Darwin Department of Histology, Faculty of Medicine, Andalas University, Padang, Indonesia
  • Yanwirasti Yanwirasti Department of Anatomy, Faculty of Medicine, Andalas University, Padang, Indonesia
  • Rizal Hamid Department of Surgery, Faculty of Medicine, Indonesia University, Jakarta, Indonesia

DOI:

https://doi.org/10.3889/oamjms.2019.548

Keywords:

Prostate Hyperplasia, Prostate Cancer, IL-6, TGFβ-1, Gleason Index

Abstract

BACKGROUND: Prostate hyperplasia and prostate cancer are two of the most common pathological condition of the prostate to be found on male. Both of these diseases share common pathogenesis involving inflammation of prostatic tissues. Chronic inflammation will induce the release of cytokines, followed by cells injury and tissues damage. One of the cytokines that play a role in prostate pathology is IL-6. The inflammation will also induce the releases of anti-inflammatory cytokines such as TGFβ-1.
AIM: This study aims to analyse the expression of IL-6 and TGFβ-1, in prostate hyperplasia and prostate cancer.
MATERIAL AND METHODS: This is an observational study, using paraffin-embedded tissue samples of prostate hyperplasia and prostate cancer. Samples were obtained from the laboratory of Pathological Anatomy, Faculty of Medicine, Andalas University, Padang, Indonesia. Immunohistochemistry was performed to detect the cytokine expression, and a semiqunatitaves measurement according to Immunoreactive score (IRS) was performed for evaluation. For the TGFβ-1, the stromal expression was also analysed by measurement of the stromal stained area. The correlation of cytokine expression to Gleason index score was also analysed in prostate cancer.
RESULTS: The result showed that this study found that TGFβ-1 was detected both in the stromal component as well as epithelial. With the stromal being the dominant site of expression. The stromal TGFβ-1 expression was of significantly higher in prostate hyperplasia compares to prostate cancer (p < 0.05), while the epithelial expression of TGFβ-1 was not found to be significantly different. IL-6 was mostly expressed intracytoplasmic in epithelia. The IL-6 expression was significantly higher in prostate cancer compared to hyperplasia. However, there was no significant correlation to found between IL-6 expression to the Gleason Score among prostate cancers.
CONCLUSION: This study concluded that there were differences in expression of both TGFβ-1 and IL-6 between prostate hyperplasia and prostate cancer tissue by immunohistochemistry.

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References

Abedelmalek S, Wong DP, Chtourou H, Souissi N, Tabka Z. Racial Variation of Interleukin-6 in Soccer Players: The Effect of Short-Term Maximal Exercise. International Journal of Medicine and Pharmaceutical Sciences (IJMPS). 2014; 4(1):37-48. https://doi.org/10.1080/09291016.2014.904574

Elkahwaji JE. The role of inflammatory mediators in the development of prostatic hyperplasia and prostate cancer. Res Rep Urol. 2012; 5:1-10. https://doi.org/10.2147/RRU.S23386 PMid:24400229 PMCid:PMC3826944

De Nunzio C, Kramer G, Marberger M, Montironi R, Nelson W, Schröder F, et al. The controversial relationship between benign prostatic hyperplasia and prostate cancer: The role of inflammation. Eur Urol. 2011; 60(1):106-17. https://doi.org/10.1016/j.eururo.2011.03.055 PMid:21497433

Gandaglia G, Briganti A, Gontero P, Mondaini N, Novara G, Salonia A, Sciarra A, Montorsi F. The role of chronic prostatic inflammation in the pathogenesis and progression of benign prostatic hyperplasia (BPH). BJU international. 2013; 112(4):432-41. https://doi.org/10.1111/bju.12118 PMid:23650937

Bardan R, Dumache R, Dema A, Cumpanas A, Bucuras V. The role of prostatic inflammation biomarkers in the diagnosis of prostate diseases. Clinical biochemistry. 2014; 47(10-11):909-15. https://doi.org/10.1016/j.clinbiochem.2014.02.008 PMid:24560954

Untergasser G, Madersbacher S, Berger P. Benign prostatic hyperplasia: age-related tissue-remodeling. Experimental gerontology. 2005; 40(3):121-8. https://doi.org/10.1016/j.exger.2004.12.008 PMid:15763388

Xu H, Hu MB, Bai PD, Zhu WH, Liu SH, Hou JY, Xiong ZQ, Ding Q, Jiang HW. Proinflammatory cytokines in prostate cancer development and progression promoted by high-fat diet. BioMed research international. 2015; 2015. https://doi.org/10.1155/2015/249741 PMid:25722971 PMCid:PMC4334627

Sciarra A, Mariotti G, Salciccia S, Gomez AA, Monti S, Toscano V, et al. Prostate growth and inflammation. J Steroid Biochem Mol Biol. 2008; 108(3-5):254-60. https://doi.org/10.1016/j.jsbmb.2007.09.013 PMid:17935971

Sfanos KS, De Marzo AM. Prostate cancer and inflammation: the evidence. Histopathology. 2012; 60(1):199-215. https://doi.org/10.1111/j.1365-2559.2011.04033.x PMid:22212087 PMCid:PMC4029103

McLaren ID, Jerde TJ, Bushman W. Role of interleukins, IGF and stem cells in BPH. Differentiation. 2011; 82(4-5):237-43. https://doi.org/10.1016/j.diff.2011.06.001 PMid:21864972 PMCid:PMC3873782

Hamid AR, Umbas R, Mochtar CA. Recent role of inflammation in prostate diseases: chemoprevention development opportunity. Acta Med Indones. 2011; 43(1):59-65.

Bergamini S, Bellei E, Bonetti LR, Monari E, Cuoghi A, Borelli F, Sighinolfi MC, Bianchi G, Ozben T, Tomasi A. Inflammation: an important parameter in the search of prostate cancer biomarkers. Proteome science. 2014; 12(1):32. https://doi.org/10.1186/1477-5956-12-32 PMid:24944525 PMCid:PMC4061775

Thapa D, Ghosh R. Chronic inflammatory mediators enhance prostate cancer development and progression. Biochemical pharmacology. 2015; 94(2):53-62. https://doi.org/10.1016/j.bcp.2014.12.023 PMid:25593038

Chughtai B, Lee R, Te A, Kaplan S. Inflammation and benign prostatic hyperplasia: clinical implications. Current urology reports. 2011; 12(4):274-7. https://doi.org/10.1007/s11934-011-0191-3 PMid:21519898

Tiwari A. Elocalcitol, a vitamin D3 analog for the potential treatment of benign prostatic hyperplasia, overactive bladder and male infertility. IDrugs: the investigational drugs journal. 2009; 12(6):381-93.

Adorini L, Penna G, Fibbi B, Maggi M. Vitamin D receptor agonists target static, dynamic, and inflammatory components of benign prostatic hyperplasia. Annals of the New York Academy of Sciences. 2010; 1193(1):146-52. https://doi.org/10.1111/j.1749-6632.2009.05299.x PMid:20398021

Manchanda PK, Kibler AJ, Zhang M, Ravi J, Bid HK. Vitamin D receptor as a therapeutic target for benign prostatic hyperplasia. Indian J Urol. 2012; 28(4):377-81. https://doi.org/10.4103/0970-1591.105745 PMid:23450267 PMCid:PMC3579114

Porcaro AB, Novella G, Molinari A, Terrin A, Minja A, De Marco V, Martignoni G, Brunelli M, Cerruto MA, Curti P, Cavalleri S. Prostate volume index and chronic inflammation of the prostate type IV with respect to the risk of prostate cancer. Urologia internationalis. 2015; 94(3):270-85. https://doi.org/10.1159/000362176 PMid:25170543

Kashyap M, Pore S, Wang Z, Gingrich J, Yoshimura N, Tyagi P. Inflammasomes are important mediators of prostatic inflammation associated with BPH. Journal of inflammation. 2015; 12(1):37. https://doi.org/10.1186/s12950-015-0082-3 PMid:25991911 PMCid:PMC4436794

Engelhardt PF, Seklehne S, Brustrmann H, et al. Immmuno Histochemical Espression of Interleukin-2 Receptor and Interleukin -6 in Patients with Prostate Cancer and Benigh Prostatic Hiperplasia: Association with asymptomatic Inflamatory Prostatitis NIH Category IV. Scan J Urol. 2014; 49(2):120-126. https://doi.org/10.3109/21681805.2014.971427 PMid:25363611

Basanta D, Strand DW, Lukner RB, et al. The Role of Transforming Growth Factor-β Mediated Tumor-Stroma Interactons in Prostate Cancer Progression: An Integrative Approach. Cancer Res. 2009; 69(17):7111-7120. https://doi.org/10.1158/0008-5472.CAN-08-3957 PMid:19706777 PMCid:PMC2748342

Funahashi Y, O'Malley KJ, Kawamorita N, et al. Upregulation of Androgen-Responsive Gen and Transforming Growth Factor β1 Cascade Genes in a Rat Model of Non-Bacterial Prostatic Inflamation. Prostate. 2014; 74(4):337-345. https://doi.org/10.1002/pros.22668 PMid:24446128 PMCid:PMC3898594

Lucia MS, Lambret JR. Growth Factor in Benign Prostatic Hyperplasia: Basic Science Implications. Curren Prostate Reports. 2007; 5:78-84. https://doi.org/10.1007/s11918-007-0011-x

Cao Z, Kyprianou N. Mechanism Navigating theTGF-β Pathway in Prostat Cancer. Asian Journal of Urology. 2015; 2:11-1. https://doi.org/10.1016/j.ajur.2015.04.011 PMid:29051866 PMCid:PMC5645057

Kattan MW, Shariat SF, Andrews B, et al. The addition of Interleukin 6 Soluble Receptor and Transformng Growth Factor Beta, improves a Preoperative Nomogram for Predicting Biochemical Progression in Patients with Clinically Located Prostate Cancer, Journal of Clinical Oncology. 2003; 21(9):3573-3579. https://doi.org/10.1200/JCO.2003.12.037 PMid:12913106

Smith PC, Hobisch A, Lin DL, et al. Interleukin 6 and Prostate Cancer Progression. Cytokine Growth Factor. Reviews. 2001; 12:33-40. https://doi.org/10.1016/S1359-6101(00)00021-6

Pace G, Di Massimo C, De Amicis D, Vicentini C, Ciancarelli MGT. Inflammation and endothelial activation in benign prostatic hyperplasia and prostate cancer. Int Braz J Urol. 2011; 37(5):617-22. https://doi.org/10.1590/S1677-55382011000500008 PMid:22099274

Cung Z, Steiner H, Bartsch, et al. Interleukin-6 Regulation of Prostate Cancer Cell Growth. Journal of Cellular Biochemistry. 2005; 95;497-505. https://doi.org/10.1002/jcb.20477 PMid:15838876

Bostanci Y, Kazzazi A, Momtahen S, Laze J, Djavan B. Correlation between benign prostatic hyperplasia and inflammation. Current opinion in urology. 2013; 23(1):5-10. https://doi.org/10.1097/MOU.0b013e32835abd4a PMid:23159991

Steiner MS, Zhou ZZ, Tonb DC, et al. Expression of Transforming Growth Factor β1 in Prostat Cancer Endocrinology. 1994; 135(5):2240-2246. https://doi.org/10.1210/endo.135.5.7956947 PMid:7956947

Flavel RA, Sanjabi S, Wrzesinski SH, et al. The Polarization of Immune Cells in the Tumor Environment by TGF-β. Nature Reviews Immunology. 2010; 10:554-567. https://doi.org/10.1038/nri2808 PMid:20616810 PMCid:PMC3885992

Zuhirman. Hubungan Transforming Growth Factor β1, Tumor Necrosis Factor α, Matrix Metallo Proteinase-1 dan Fibroblast Growth Factor 2 dengan Fibrosis Ureter pada penderita batu ureter. Disertasi; Fakultas Kedokteran Universitas Andalas Padang, 2014:133-139.

Duscharla D, Reddy KRK, Dasari C, et al. Interleukin-6 Induced Over expression of valosin-Containing Protein (VCP) / p97 is Associated with Androgen-Independent Prostate Cancer (AIPC) Progession Wiley Cellular Physiology. 2018; 1-17. https://doi.org/10.1002/jcp.26639 PMid:29693262

Illiopoulos, D., Hirsch, H.A and Struhl, K. An epigenetic switch involving NF-kB, Lin28, let-7 microRNA, and IL6 links inflammation to cell transformation. Cell. 2009; 139(4):693-706. https://doi.org/10.1016/j.cell.2009.10.014 PMid:19878981 PMCid:PMC2783826

Published

2019-07-02

How to Cite

1.
Afdal A, Darwin E, Yanwirasti Y, Hamid R. The Expression of Transforming Growth Factor Beta-1 and Interleukin-6 on Human Prostate: Prostate Hyperplasia and Prostate Cancer. Open Access Maced J Med Sci [Internet]. 2019 Jul. 2 [cited 2024 Apr. 19];7(12):1905-10. Available from: https://oamjms.eu/index.php/mjms/article/view/oamjms.2019.548

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Section

A - Basic Science

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