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Expression and mechanism of action of the SARI tumor suppressor in prostate cancer

机译:SARI抑癌基因在前列腺癌中的表达及其作用机制

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摘要

The objective of this study was to assess the expression of SARI (Suppressor of AP-1, Regulated by IFN) in prostate cancer (Pca) and explore the effects and possible mechanism of action of SARI in the occurrence and development of Pca. In the current study, the expression of SARI was detected using PCR in 40 patients with prostate cancer, 20 patients with prostatic hyperplasia, and prostate cancer cells (LNCaP. and DU145). In addition, the effects of the pro-inflammatory cytokine interferon (IFN)-β on the expression of SARI in DU145 prostate cancer cells and the possible potential signaling pathways activated by SARI were detected using RT-PCR. The expression of SARI protein was downregulated from 0.6957 ± 0.0104 to 0.1597 ± 0.0032 in prostate cancer cells compared with normal prostate tissues and cells. In addition, SARI gene expression increased from 0.0794 ± 0.0133 to 0.1232 ± 0.0162 significantly in a concentration- and time-dependent manner in DU145 cells treated with IFN-β (P<0.05). Finally, MTT assays demonstrated that DU145 cells growth slowed down, flow cytometry demonstrated that IFN-β induced apoptosis increased from 0.0343 ± 0.0039 to 0.0612 + 0.0025 in DU145 prostate cancer cells. In conclusion, the results of the current study suggest that SARI might play an important role in the occurrence and development of prostate cancer. In addition, IFN-β might inhibit the growth of prostate cancer and promote cellular apoptosis by inducing the expression of SARI.
机译:这项研究的目的是评估前列腺癌(Pca)中SARI(AP-1抑制剂,受IFN调节)的表达,并探讨SARI在Pca发生和发展中的作用及其可能的作用机制。在本研究中,使用PCR检测了40例前列腺癌患者,20例前列腺增生患者和前列腺癌细胞(LNCaP。和DU145)中SARI的表达。另外,使用RT-PCR检测促炎细胞因子干扰素(IFN)-β对DU145前列腺癌细胞中SARI表达的影响以及由SARI激活的可能的潜在信号通路。与正常前列腺组织和细胞相比,SARI蛋白在前列腺癌细胞中的表达从0.6957±0.0104下调至0.1597±0.0032。另外,在用IFN-β处理的DU145细胞中,SARI基因表达以浓度和时间依赖性的方式从0.0794±0.0133显着增加到0.1232±0.0162(P <0.05)。最后,MTT分析证实DU145前列腺癌细胞中DU145细胞的生长减慢,流式细胞仪证实IFN-β诱导的凋亡从0.0343±0.0039增加到0.0612 + 0.0025。总之,当前研究的结果表明,SARI可能在前列腺癌的发生和发展中起重要作用。另外,IFN-β可能通过诱导SARI的表达来抑制前列腺癌的生长并促进细胞凋亡。

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