Assessing the role of MSH2 and MSH6 gene expression deficiency in prostate cancer progression, a cross-sectional study

Fatemeh Sharbati, Hedieh Moradi Tabriz, Elham Nazar
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引用次数: 0

Abstract

Background

Recently, some evidence emphasized the value of MSH2 and MSH6 inactivation and their hypermutation in predicting different cancers. The present consideration is to evaluate the value of MSH2 and MSH6 protein deficient studied by the immunohistochemistry (IHC) method and the tumor behaviors and aggressiveness in prostatic carcinoma.

Methods

This cross-sectional study was performed on 80 examples extricated from patients who endured prostate cancer and were planned for radical prostatectomy surgery. The expression levels of the genes were studied by IHC staining.

Results

The deficiency in MSH2 and MSH6 expression was revealed in 10.0 % and 11.3 % of patients respectively, while the reduction of simultaneous expression in two genes was found in 6.2 % of patients. In the two subgroups with and without MSH2 and/or MSH6 staining, there was no difference in patients' mean age and history of prostate cancer. There was also no difference in tumor-related behaviors including combined Gleason grade group, tumor stage, vascular invasion, perineural invasion, and prostatic capsular invasion between the groups with and without gene loss.

Conclusion

The evaluation of the deficient rate of two genes among patients with prostate cancer to predict the tumor grade and its aggressive behavior needs further study in every population.

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一项横断面研究:评估 MSH2 和 MSH6 基因表达缺陷在前列腺癌进展中的作用。
背景:最近,一些证据强调了MSH2和MSH6失活及其高突变在预测不同癌症中的价值。本研究旨在评估通过免疫组化(IHC)方法研究的 MSH2 和 MSH6 蛋白缺失与前列腺癌的肿瘤行为和侵袭性的价值:这项横断面研究的对象是从前列腺癌患者中提取的80个样本,这些患者计划接受前列腺癌根治术。结果:MSH2和MSH3的缺失导致前列腺癌的发生:结果:10.0%和11.3%的患者发现MSH2和MSH6表达不足,6.2%的患者发现两个基因同时表达减少。在有 MSH2 和/或 MSH6 染色和无 MSH2 和/或 MSH6 染色的两个亚组中,患者的平均年龄和前列腺癌病史没有差异。基因缺失组和未缺失组在肿瘤相关行为(包括合并格里森分级组、肿瘤分期、血管侵犯、神经周围侵犯和前列腺囊侵犯)方面也没有差异:对前列腺癌患者中两种基因的缺失率进行评估,以预测肿瘤分级及其侵袭行为,需要在所有人群中进行进一步研究。
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来源期刊
CiteScore
4.30
自引率
0.00%
发文量
148
审稿时长
56 days
期刊介绍: Cancer Treatment and Research Communications is an international peer-reviewed publication dedicated to providing comprehensive basic, translational, and clinical oncology research. The journal is devoted to articles on detection, diagnosis, prevention, policy, and treatment of cancer and provides a global forum for the nurturing and development of future generations of oncology scientists. Cancer Treatment and Research Communications publishes comprehensive reviews and original studies describing various aspects of basic through clinical research of all tumor types. The journal also accepts clinical studies in oncology, with an emphasis on prospective early phase clinical trials. Specific areas of interest include basic, translational, and clinical research and mechanistic approaches; cancer biology; molecular carcinogenesis; genetics and genomics; stem cell and developmental biology; immunology; molecular and cellular oncology; systems biology; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; cancer policy; and integration of various approaches. Our mission is to be the premier source of relevant information through promoting excellence in research and facilitating the timely translation of that science to health care and clinical practice.
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