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首页> 外文期刊>American Journal of Cancer Research >Histone deacetylase 3 inhibits new tumor suppressor gene DTWD1 in gastric cancer
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Histone deacetylase 3 inhibits new tumor suppressor gene DTWD1 in gastric cancer

机译:组蛋白脱乙酰基酶3抑制胃癌新的抑癌基因DTWD1

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Cancer epigenetics plays an important role in the pathogenesis of many cancers including gastric cancer. Histone deacetylases (HDACs) emerge as exciting therapeutic targets for cancer treatment and prevention. In this study, we identified DTWD1 as one of the 122 genes upregulated after treatment of trichostatin A (TSA) in two gastric cancer cell lines. Moreover, DTWD1 was downregulated in gastric cancer cell lines and primary gastric carcinoma tissues. It was further identified as the new target of p53. Then we revealed that HDAC3 downregulated DTWD1 by disrupting the interaction of p53 with DTWD1 promoter. Furthermore, DTWD1 functioned as a tumor suppressor by downregulating cyclin B1 expression to inhibit proliferation. In summary, as the new p53 target gene, DTWD1 was downregulated in gastric cancer by HDAC3 and acted as a novel tumor suppressor gene. Specific inhibitors of HDAC3 might be a new approach for gastric cancer treatment by activating DTWD1 expression.
机译:癌症表观遗传学在包括胃癌在内的许多癌症的发病机理中起着重要作用。组蛋白脱乙酰基酶(HDAC)成为癌症治疗和预防中令人兴奋的治疗靶标。在这项研究中,我们确定DTWD1是在两种胃癌细胞系中处理曲古抑菌素A(TSA)后上调的122个基因之一。此外,DTWD1在胃癌细胞系和原发性胃癌组织中下调。它被进一步确定为p53的新靶标。然后我们揭示了HDAC3通过破坏p53与DTWD1启动子的相互作用来下调DTWD1。此外,DTWD1通过下调细胞周期蛋白B1的表达来抑制肿瘤增殖,从而起到抑癌作用。总之,作为新的p53靶基因,DTWD1在胃癌中被HDAC3下调,并作为一种新型的肿瘤抑制基因。 HDAC3的特异性抑制剂可能是通过激活DTWD1表达来治疗胃癌的一种新方法。

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