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首页> 外文期刊>OncoTargets and therapy >HOPX Is an Epigenetically Inactivated Tumor Suppressor and Overexpression of HOPX Induce Apoptosis and Cell Cycle Arrest in Breast Cancer
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HOPX Is an Epigenetically Inactivated Tumor Suppressor and Overexpression of HOPX Induce Apoptosis and Cell Cycle Arrest in Breast Cancer

机译:Hopx是一种表述灭活的肿瘤抑制和跳跃诱导患者患者凋亡和细胞循环骤停血的过表达

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Background: Evidence has been shown that abnormal DNA methylation plays a vital role in the progression of breast cancer via silencing of gene expression. The results of bisulfite sequencing showed that the methylation status of HOPX in breast cancer tissues was higher than that in normal breast cancer tissues, but little known about the biological functions of HOPX in breast cancer. Methods: A total of 13 paired breast cancer and adjacent noncancerous tissues were subjected to bisulfite sequencing. Meanwhile, the methylation levels of cg218995965 and cg24862548 in breast cancer cells were detected by methylation-specific PCR (MSP). Flow cytometry, wound healing and transwell invasion assays were used to detect the apoptosis, migration and invasion in breast cancer cells. In addition, the expressions of HOPX, p21, cyclin D1 and CDK4 in cells were detected with Western blot assay. Results: Bisulfite sequencing indicated that the CpG sites (cg218995965 and cg24862548) in the HOPX promoter region showed significantly higher methylation in breast cancer tissues. In addition, methylation-specific PCR revealed that HOPX was significantly hypermethylated in breast cancer cell lines MDA-MB-468 and MCF-7. Furthermore, overexpression of HOPX significantly inhibited the proliferation of MDA-MB-468 and MCF-7 cells via inducing the apoptosis. Moreover, upregulation of HOPX markedly inhibited the migration and invasion abilities of MDA-MB-468 cells. Meanwhile, overexpression of HOPX obviously induced cell cycle arrest in MDA-MB-468 cells via upregulation of p21, and downregulation of cyclin D1 and CDK4. Additionally, overexpression of HOPX suppressed tumor growth of breast cancer in vivo. Conclusion: Our data showed that HOPX, a tumor suppressor, is epigenetically silenced in breast cancer. Overexpression of HOPX could suppress the progression of breast cancer, and thus indicating that it might serve as a potential target for the treatment of patients with breast cancer.
机译:背景:已经表明证据表明,DNA甲基化异常在乳腺癌的进展中发挥着至关重要的作用,通过沉默基因表达。亚硫酸氢盐测序的结果表明,乳腺癌组织中HOPX的甲基化状态高于正常乳腺癌组织中的甲基化状态,但对乳腺癌跳蚤的生物学功能鲜为人知。方法:对13种成对的乳腺癌和相邻的非癌症组织进行亚硫酸氢盐测序。同时,通过甲基化特异性PCR(MSP)检测乳腺癌细胞中CG218995965和CG24862548的甲基化水平。流式细胞术,伤口愈合和Transwell入侵测定用于检测乳腺癌细胞中的凋亡,迁移和侵袭。另外,用蛋白质印迹测定检测Hopx,P21,Cyclin D1和CDK4中的表达。结果:Bisulfite测序表明,跳跃启动子区域中的CPG位点(CG218995965和CG24862548)显示出乳腺癌组织中的甲基化显着较高。此外,甲基化特异性PCR显示HOPX在乳腺癌细胞系MDA-MB-468和MCF-7中显着高甲甲基化。此外,HOPX的过表达通过诱导细胞凋亡显着抑制MDA-MB-468和MCF-7细胞的增殖。此外,HOPX的上调显着抑制MDA-MB-468细胞的迁移和侵袭能力。同时,HOPX的过度表达通过P21的上调和细胞周期蛋白D1和CDK4的下调,过表达明显诱导MDA-MB-468细胞中的细胞周期停滞。另外,跳跃的过表达抑制体内乳腺癌的肿瘤生长。结论:我们的数据显示HOPX,肿瘤抑制剂,在乳腺癌中表现出脑膜肠道。 Hopx的过度表达可以抑制乳腺癌的进展,从而表明它可能是治疗乳腺癌患者的潜在目标。

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