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微小RNA-219-5p通过靶向致癌基因Sall4在结肠癌中发挥肿瘤抑制作用。

miR-219-5p plays a tumor suppressive role in colon cancer by targeting oncogene Sall4.

作者信息

Cheng Ji, Deng Rui, Zhang Peng, Wu Chuanqing, Wu Ke, Shi Liang, Liu Xinghua, Bai Jie, Deng Meizhou, Shuai Xiaoming, Gao Jinbo, Wang Guobin, Tao Kaixiong

机构信息

Department of Gastrointestinal Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, P.R. China.

出版信息

Oncol Rep. 2015 Oct;34(4):1923-32. doi: 10.3892/or.2015.4168. Epub 2015 Aug 4.

Abstract

Sall4 is a novel oncogene found upregulated in several malignancies including colon cancer. However, its upstream regulatory miRNA is still undefined. miR-219-5p is regarded as a tumor-related miRNA in cancer research. Nevertheless, its actual role of whether inhibiting or promoting tumorigenesis is unclear in colon cancer. Potential interaction between Sall4 and miR-219-5p is predicted by TargetScan. CCK-8 test was used for evaluation of cell proliferation and cell survival rates. Western blot analysis and real-time PCR were applied for detection of target molecules. Luciferase assay was a direct confirmation of mutual interaction. Wound healing assay and transwell assay were conducted for cell migration and invasion tests. Flow cytometry was used for cell apoptosis analysis. Tissue specimens and cell lines were explored for miR-219-5p inhibition on colon cancer proliferation, migration, invasion, apoptosis and drug resistance by targeting Sall4. The results show that miR-219-5p inhibited carcinogenesis of colon cancer by targeting oncogene Sall4.

摘要

Sall4是一种新发现的癌基因,在包括结肠癌在内的多种恶性肿瘤中上调。然而,其上游调控miRNA仍不明确。在癌症研究中,miR-219-5p被视为一种肿瘤相关miRNA。然而,在结肠癌中,其抑制或促进肿瘤发生的实际作用尚不清楚。TargetScan预测了Sall4与miR-219-5p之间的潜在相互作用。采用CCK-8试验评估细胞增殖和细胞存活率。应用蛋白质免疫印迹分析和实时荧光定量PCR检测靶分子。荧光素酶报告基因检测直接证实了两者之间的相互作用。采用划痕试验和Transwell试验进行细胞迁移和侵袭试验。采用流式细胞术进行细胞凋亡分析。通过靶向Sall4,研究组织标本和细胞系中miR-219-5p对结肠癌增殖、迁移、侵袭、凋亡和耐药性的影响。结果表明,miR-219-5p通过靶向癌基因Sall4抑制结肠癌的发生。

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