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miR-98通过靶向IGF1R抑制糖尿病合并结肠癌患者肿瘤增殖和侵袭的机制

Mechanism of miR-98 inhibiting tumor proliferation and invasion by targeting IGF1R in diabetic patients combined with colon cancer.

作者信息

Liu Shixiong, Zhou Yun, Zhou Yongning, Wang Jing, Ji Rui

机构信息

Department of Geriatrics (II), The First Hospital of Lanzhou University, Lanzhou, Gansu 730000, P.R. China.

Department of Gastroenterology, The First Hospital of Lanzhou University, Lanzhou, Gansu 730000, P.R. China.

出版信息

Oncol Lett. 2020 Aug;20(2):1719-1726. doi: 10.3892/ol.2020.11707. Epub 2020 Jun 9.

Abstract

Expression level of miR-98 in diabetic colon cancer (CRC) tissues and the regulation mechanism of colon cancer cell proliferation and invasion ability were studied. Forty patients with type 2 diabetes mellitus complicated with colon cancer, 40 colon cancer patients, and 40 patients with diabetic colonoscopy were enrolled between January 2017 and January 2018. Real-time quantitative PCR was used to detect the expression level of miR-98. After SW480 cells were transfected with miR-98 mimics or control simulants, the proliferation of cancer cells was detected by MTT assay, and the invasion ability of cancer cells was detected by Transwell cell invasion assay. The dual luciferase assay was used to detect the binding relationship between miR-98 and IGF1R. Western blot analysis was used to detect the expression of IGF1R protein in tumor tissues of patients with diabetes mellitus and colon cancer. Compared with diabetic patients, the expression level of miR-98 was decreased in colon cancer patients. Compared with tumor tissues of colon cancer patients, the expression level of miR-98 was significantly decreased in diabetic colon cancer tissues. Compared with the commonly cultured colon cancer SW480 cells, the expression level of miR-98 was significantly decreased in SW480 cells cultured under high glucose conditions. Increased expression of miR-98 inhibits colon cancer cell proliferation and invasion. miR-98 can target and bind to IGF1R and inhibit its expression level. IGF1R is upregulated in diabetic colon cancer tissue. miR-98 inhibits proliferation and invasion of diabetic colon cancer by targeting IGF1R. The expression level of miR-98 in diabetic colon cancer tissues is lower than that in colon cancer tissues. miR-98 can inhibit the proliferation and invasion of colon cancer cells by targeting the target gene IGF1R. miR-98 may be a potential biological target for the treatment of patients with diabetes and colon cancer.

摘要

研究了miR-98在糖尿病结肠癌(CRC)组织中的表达水平以及对结肠癌细胞增殖和侵袭能力的调控机制。2017年1月至2018年1月期间纳入了40例2型糖尿病合并结肠癌患者、40例结肠癌患者和40例糖尿病结肠镜检查患者。采用实时定量PCR检测miR-98的表达水平。用miR-98模拟物或对照模拟物转染SW480细胞后,通过MTT法检测癌细胞的增殖情况,通过Transwell细胞侵袭试验检测癌细胞的侵袭能力。采用双荧光素酶报告基因检测法检测miR-98与IGF1R的结合关系。采用蛋白质免疫印迹分析检测糖尿病和结肠癌患者肿瘤组织中IGF1R蛋白的表达。与糖尿病患者相比,结肠癌患者中miR-98的表达水平降低。与结肠癌患者的肿瘤组织相比,糖尿病结肠癌组织中miR-98的表达水平显著降低。与普通培养的结肠癌SW480细胞相比,在高糖条件下培养的SW480细胞中miR-98的表达水平显著降低。miR-98表达增加可抑制结肠癌细胞的增殖和侵袭。miR-98可靶向并结合IGF1R并抑制其表达水平。IGF1R在糖尿病结肠癌组织中上调。miR-98通过靶向IGF1R抑制糖尿病结肠癌的增殖和侵袭。糖尿病结肠癌组织中miR-98的表达水平低于结肠癌组织。miR-98可通过靶向靶基因IGF1R抑制结肠癌细胞的增殖和侵袭。miR-98可能是治疗糖尿病和结肠癌患者的潜在生物学靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e09/7377170/d3eb79eae64a/ol-20-02-1719-g00.jpg

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