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Altered expression of PTCH and HHIP in gastric cancer through their gene promoter methylation: Novel targets for gastric cancer

机译:通过基因启动子甲基化改变胃癌中PTCH和HHIP的表达:胃癌的新靶点

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Human hedgehog-interacting protein (HHIP) and protein patched homolog (PTCH) are two negative regulators of the hedgehog signal, however, the mechanism of action in gastric cancer is unknown. Methylation of TSG promoters has been considered as a causative mechanism of tumorigenesis. In the present study, we first determined the expression of PTCH and HHIP mRNA and protein in gastric cancer tissues and adjacent normal tissues, and then detected methylation of the two genes to associate their expression and gene promoter methylation in gastric cancer. Expression in gastric cancer tissues and the cancer cells (AGS) were evaluated by reverse transcription-PCR (RT-PCR), qRT-PCR and IHC, while the methylation expression was valued by methylation-specific PCR (MSP) and bisulfite sequencing PCR (BSP). Cell viability and apoptosis were analyzed by MTT assay and flow cytometry following treatment with 5-aza-dc. Results showed that PTCH and HHIP expression was reduced in gastric cancer tissues that were not associated with clinical features. Moreover, methylation of the promoters was reversely correlated with the expression. Following treatment with 5-aza-dc, AGS reduced cell viability and induced apoptosis, which is associated with upregulation of HHIP expression. The data demonstrated that loss of expression of HHIP and PTCH is associated with the methylation of gene promoters. In addition, 5-aza-dc-induced apoptosis correlated with the upregulation of HHIP expression in AGS. The findings demonstrated that the PTCH and HHIP genes may be novel targets for the control of gastric cancer.
机译:人刺猬相互作用蛋白(HHIP)和蛋白修补同源物(PTCH)是刺猬信号的两个负调控因子,但是,在胃癌中的作用机理尚不清楚。 TSG启动子的甲基化被认为是肿瘤发生的致病机制。在本研究中,我们首先确定PTCH和HHIP mRNA和蛋白在胃癌组织和邻近正常组织中的表达,然后检测这两个基因的甲基化以使其在胃癌中的表达与基因启动子甲基化相关。胃癌组织和癌细胞(AGS)中的表达通过逆转录PCR(RT-PCR),qRT-PCR和IHC进行评估,而甲基化表达则通过甲基化特异性PCR(MSP)和亚硫酸氢盐测序PCR( BSP)。用5-氮杂-dc处理后,通过MTT测定和流式细胞术分析细胞活力和凋亡。结果表明,与临床特征无关的胃癌组织中PTCH和HHIP表达降低。此外,启动子的甲基化与表达反向相关。用5-氮杂-dc处理后,AGS降低细胞活力并诱导凋亡,这与HHIP表达的上调有关。数据表明,HHIP和PTCH表达的缺失与基因启动子的甲基化有关。另外,5-氮杂-dc-诱导的凋亡与AGS中HHIP表达的上调相关。这些发现表明,PTCH和HHIP基因可能是控制胃癌的新靶标。

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