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The tumor suppressor Zinc finger protein 471 suppresses breast cancer growth and metastasis through inhibiting AKT and Wnt/β-catenin signaling
Clinical Epigenetics ( IF 4.8 ) Pub Date : 2020-11-17 , DOI: 10.1186/s13148-020-00959-6
Chunfang Tao 1 , Juan Luo 1 , Jun Tang 1 , Danfeng Zhou 1 , Shujun Feng 2 , Zhu Qiu 1 , Thomas C Putti 3 , Tingxiu Xiang 1 , Qiao Tao 1, 4 , Lili Li 4 , Guosheng Ren 1
Affiliation  

Zinc-finger protein 471 (ZNF471) is a member of the Krüppel-associated box domain zinc finger protein (KRAB-ZFP) family. ZNF471 is methylated in squamous cell carcinomas of tongue, stomach and esophageal. However, its role in breast carcinogenesis remains elusive. Here, we studied its expression, functions, and molecular mechanisms in breast cancer. We examined ZNF471 expression by RT-PCR and qPCR. Methylation-specific PCR determined its promoter methylation. Its biological functions and related molecular mechanisms were assessed by CCK-8, clonogenicity, wound healing, Transwell, nude mice tumorigenicity, flow cytometry, BrdU-ELISA, immunohistochemistry and Western blot assays. ZNF471 was significantly downregulated in breast cell lines and tissues due to its promoter CpG methylation, compared with normal mammary epithelial cells and paired surgical-margin tissues. Ectopic expression of ZNF471 substantially inhibited breast tumor cell growth in vitro and in vivo, arrested cell cycle at S phase, and promoted cell apoptosis, as well as suppressed metastasis. Further knockdown of ZNF471 verified its tumor-suppressive effects. We also found that ZNF471 exerted its tumor-suppressive functions through suppressing epithelial-mesenchymal transition, tumor cell stemness and AKT and Wnt/β-catenin signaling. ZNF471 functions as a tumor suppressor that was epigenetically inactivated in breast cancer. Its inhibition of AKT and Wnt/β-catenin signaling pathways is one of the mechanisms underlying its anti-cancer effects.

中文翻译:

肿瘤抑制因子锌指蛋白 471 通过抑制 AKT 和 Wnt/β-catenin 信号传导抑制乳腺癌的生长和转移

锌指蛋白 471 (ZNF471) 是 Krüppel 相关框域锌指蛋白 (KRAB-ZFP) 家族的成员。ZNF471 在舌、胃和食道的鳞状细胞癌中甲基化。然而,它在乳腺癌发生中的作用仍然难以捉摸。在这里,我们研究了它在乳腺癌中的表达、功能和分子机制。我们通过 RT-PCR 和 qPCR 检查了 ZNF471 的表达。甲基化特异性 PCR 确定其启动子甲基化。通过CCK-8、克隆形成、伤口愈合、Transwell、裸鼠致瘤性、流式细胞术、BrdU-ELISA、免疫组织化学和Western印迹分析评估其生物学功能和相关分子机制。由于其启动子 CpG 甲基化,ZNF471 在乳腺细胞系和组织中显着下调,与正常乳腺上皮细胞和成对的手术边缘组织相比。ZNF471 的异位表达在体外和体内显着抑制乳腺肿瘤细胞的生长,使细胞周期停滞在 S 期,促进细胞凋亡,并抑制转移。ZNF471 的进一步敲低证实了其肿瘤抑制作用。我们还发现 ZNF471 通过抑制上皮间质转化、肿瘤细胞干性和 AKT 和 Wnt/β-catenin 信号传导发挥其肿瘤抑制功能。ZNF471 作为一种肿瘤抑制因子,在乳腺癌中表观遗传失活。其对AKT和Wnt/β-catenin信号通路的抑制是其抗癌作用的机制之一。抑制细胞周期在S期,促进细胞凋亡,抑制转移。ZNF471 的进一步敲低证实了其肿瘤抑制作用。我们还发现 ZNF471 通过抑制上皮间质转化、肿瘤细胞干性和 AKT 和 Wnt/β-catenin 信号传导发挥其肿瘤抑制功能。ZNF471 作为一种肿瘤抑制因子,在乳腺癌中表观遗传失活。其对AKT和Wnt/β-catenin信号通路的抑制是其抗癌作用的机制之一。抑制细胞周期在S期,促进细胞凋亡,抑制转移。ZNF471 的进一步敲低证实了其肿瘤抑制作用。我们还发现 ZNF471 通过抑制上皮间质转化、肿瘤细胞干性和 AKT 和 Wnt/β-catenin 信号传导发挥其肿瘤抑制功能。ZNF471 作为一种肿瘤抑制因子,在乳腺癌中表观遗传失活。其对AKT和Wnt/β-catenin信号通路的抑制是其抗癌作用的机制之一。肿瘤细胞干性和 AKT 和 Wnt/β-catenin 信号传导。ZNF471 作为一种肿瘤抑制因子,在乳腺癌中表观遗传失活。其对AKT和Wnt/β-catenin信号通路的抑制是其抗癌作用的机制之一。肿瘤细胞干性和 AKT 和 Wnt/β-catenin 信号传导。ZNF471 作为一种肿瘤抑制因子,在乳腺癌中表观遗传失活。其对AKT和Wnt/β-catenin信号通路的抑制是其抗癌作用的机制之一。
更新日期:2020-11-17
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