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miR-34b的差异表达与雄激素受体途径调节非裔美国人和高加索人前列腺癌侵袭性的差异。

Differential expression of miR-34b and androgen receptor pathway regulate prostate cancer aggressiveness between African-Americans and Caucasians.

作者信息

Shiina Marisa, Hashimoto Yutaka, Kato Taku, Yamamura Soichiro, Tanaka Yuichiro, Majid Shahana, Saini Sharanjot, Varahram Shahryari, Kulkarni Priyanka, Dasgupta Pritha, Mitsui Yozo, Sumida Mitsuho, Tabatabai Laura, Deng Guoren, Kumar Deepak, Dahiya Rajvir

机构信息

Department of Urology, Veterans Affairs Medical Center, San Francisco and University of California San Francisco, San Francisco, California, USA.

Division of Science and Mathematic, Cancer Research Laboratory, University of the District of Columbia, Washington, DC, USA.

出版信息

Oncotarget. 2017 Jan 31;8(5):8356-8368. doi: 10.18632/oncotarget.14198.

Abstract

African-Americans are diagnosed with more aggressive prostate cancers and have worse survival than Caucasians, however a comprehensive understanding of this health disparity remains unclear. To clarify the mechanisms leading to this disparity, we analyzed the potential involvement of miR-34b expression in African-Americans and Caucasians. miR-34b functions as a tumor suppressor and has a multi-functional role, through regulation of cell proliferation, cell cycle and apoptosis. We found that miR-34b expression is lower in human prostate cancer tissues from African-Americans compared to Caucasians. DNA hypermethylation of the miR-34b-3p promoter region showed significantly higher methylation in prostate cancer compared to normal samples. We then sequenced the promoter region of miR-34b-3p and found a chromosomal deletion in miR-34b in African-American prostate cancer cell line (MDA-PCA-2b) and not in Caucasian cell line (DU-145). We found that AR and ETV1 genes are differentially expressed in MDA-PCa-2b and DU-145 cells after overexpression of miR-34b. Direct interaction of miR-34b with the 3' untranslated region of AR and ETV1 was validated by luciferase reporter assay. We found that miR-34b downregulation in African-Americans is inversely correlated with high AR levels that lead to increased cell proliferation. Overexpression of miR-34b in cell lines showed higher inhibition of cell proliferation, apoptosis and G1 arrest in the African-American cells (MDA-PCa-2b) compared to Caucasian cell line (DU-145). Taken together, our results show that differential expression of miR-34b and AR are associated with prostate cancer aggressiveness in African-Americans.

摘要

非裔美国人被诊断出患有更具侵袭性的前列腺癌,且其生存率低于白种人,然而对这种健康差异的全面理解仍不明确。为了阐明导致这种差异的机制,我们分析了非裔美国人和白种人中miR-34b表达的潜在作用。miR-34b作为一种肿瘤抑制因子,通过调节细胞增殖、细胞周期和凋亡发挥多功能作用。我们发现,与白种人相比,非裔美国人的人类前列腺癌组织中miR-34b表达较低。与正常样本相比,前列腺癌中miR-34b-3p启动子区域的DNA高甲基化显示出明显更高的甲基化水平。然后我们对miR-34b-3p的启动子区域进行测序,发现在非裔美国人前列腺癌细胞系(MDA-PCA-2b)中miR-34b存在染色体缺失,而在白种人细胞系(DU-145)中没有。我们发现,在过表达miR-34b后,AR和ETV1基因在MDA-PCa-2b和DU-145细胞中的表达存在差异。荧光素酶报告基因检测验证了miR-34b与AR和ETV1的3'非翻译区直接相互作用。我们发现,非裔美国人中miR-34b的下调与导致细胞增殖增加的高AR水平呈负相关。与白种人细胞系(DU-145)相比,在细胞系中过表达miR-34b对非裔美国人细胞(MDA-PCa-2b)的细胞增殖、凋亡和G1期阻滞具有更高的抑制作用。综上所述,我们的结果表明,miR-34b和AR的差异表达与非裔美国人前列腺癌的侵袭性有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd49/5352406/8dadd84598f4/oncotarget-08-8356-g001.jpg

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