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CCDC43-ADRM1 轴受 YY1 调控,促进胃癌的增殖和转移。

The CCDC43-ADRM1 axis regulated by YY1, promotes proliferation and metastasis of gastric cancer.

机构信息

Guangdong Provincial Key Laboratory of Gastroenterology, Department of Gastroenterology, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China.

Department of Gastroenterology, Longgang District People's Hospital, Shenzhen, 518172, China.

出版信息

Cancer Lett. 2020 Jul 10;482:90-101. doi: 10.1016/j.canlet.2020.03.026. Epub 2020 Apr 8.

Abstract

Previous studies have shown an association between coiled-coil domain-containing (CCDC) genes and different cancers. Our previous studies revealed that CCDC43 is highly expressed in colorectal cancer, but the expression and molecular mechanisms of CCDC43 in gastric cancer (GC) are yet to be determined. Here, we show that CCDC43 is overexpressed in gastric tissues. CCDC43 expression is closely related to tumor differentiation, lymph-node-metastasis, and prognosis of gastric cancer. Overexpression of CCDC43 promotes the proliferation, invasion, and metastasis of GC cells. CCDC43 may upregulate and stabilize ADRM1, resulting in the construction of the ubiquitin-mediated proteasome. In contrast, inhibition of ADRM1 could reverse the function of CCDC43 in GC both in vitro and in vivo. Our data demonstrate that transcription factor YY1 directly binds to CCDC43 and ADRM1 gene promoters, leading to over-expression of CCDC43 and ADRM1. Furthermore, in vitro experiments demonstrate that knock down of CCDC43 or ADRM1 attenuates the YY1-mediated malignant phenotypes. Finally, the association among YY1, CCDC43 and ADRM1 is validated in clinical samples. Our findings suggest that the CCDC43-ADRM1 axis regulated by YY1, promotes proliferation and metastasis of GC, and the axis may be a potential therapeutic target for GC.

摘要

先前的研究表明卷曲螺旋结构域蛋白(CCDC)基因与多种癌症有关。我们之前的研究表明 CCDC43 在结直肠癌中高表达,但 CCDC43 在胃癌(GC)中的表达和分子机制尚未确定。在这里,我们显示 CCDC43 在胃组织中过表达。CCDC43 的表达与肿瘤分化、淋巴结转移和胃癌的预后密切相关。CCDC43 的过表达促进 GC 细胞的增殖、侵袭和转移。CCDC43 可能上调并稳定 ADRM1,从而构建泛素介导的蛋白酶体。相反,ADRM1 的抑制作用可以在体外和体内逆转 CCDC43 在 GC 中的功能。我们的数据表明转录因子 YY1 直接与 CCDC43 和 ADRM1 基因启动子结合,导致 CCDC43 和 ADRM1 的过表达。此外,体外实验表明,CCDC43 或 ADRM1 的敲低减弱了 YY1 介导的恶性表型。最后,在临床样本中验证了 YY1、CCDC43 和 ADRM1 之间的关联。我们的研究结果表明,YY1 调节的 CCDC43-ADRM1 轴促进了 GC 的增殖和转移,该轴可能是 GC 的潜在治疗靶点。

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