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微小RNA-92b-3p通过抑制KLF3促进结肠癌发展。

microRNA-92b-3p augments colon cancer development through inhibiting KLF3.

作者信息

Liu Xuezhong, Zhang Lei

机构信息

Department of Gastrointestinal Surgery, Liaocheng People's Hospital, Liaocheng, Shandong, China.

Department of General Surgery, Liaocheng Dongchangfu People's Hospital, Liaocheng, Shandong, China.

出版信息

J Biochem Mol Toxicol. 2023 Dec;37(12):e23488. doi: 10.1002/jbt.23488. Epub 2023 Aug 19.

DOI:10.1002/jbt.23488
PMID:37597242
Abstract

Colon cancer (CC) is a tumor of the large intestine. miR-92b-3p is often deregulated in the tumorigensis. Here, the role of miR-92b-3p in the development of CC was investigated. miR-92b-3p and Kruppel-like factor 3 (KLF3) expression was examined in CC tissues and cells. miR-92b-3p inhibitor or KLF3 overexpression vector was transfected into CC cells, respectively to observe its role in CC cell proliferation, invasion, migration, and apoptosis. The targeting relationship between miR-92b-3p and KLF3 was validated. Meanwhile, rescue experiments were performed by co-transfection of miR-92b-3p inhibitor and KLF3 siRNA, followed by determining CC cell proliferation, invasion, migration, and apoptosis. Higher miR-92b-3p and lower KLF3 expression levels were observed in CC tissues and cells. miR-92b-3p inhibition or KLF3 overexpression reduced proliferation, invasion, and migration whereas induced apoptosis of CC cells. KLF3 was validated to be the target gene of miR-92b-3p. Depletion of KLF3 could reverse the antitumor role of miR-92b-3p inhibition in CC cells. miR-92b-3p augments CC development through inhibiting KLF3, which may confers a novel way to develop future treatment target.

摘要

结肠癌(CC)是一种大肠肿瘤。miR-92b-3p在肿瘤发生过程中常常失调。在此,研究了miR-92b-3p在CC发生发展中的作用。检测了CC组织和细胞中miR-92b-3p和 Kruppel样因子3(KLF3)的表达。将miR-92b-3p抑制剂或KLF3过表达载体分别转染到CC细胞中,以观察其在CC细胞增殖、侵袭、迁移和凋亡中的作用。验证了miR-92b-3p与KLF3之间的靶向关系。同时,通过共转染miR-92b-3p抑制剂和KLF3 siRNA进行挽救实验,随后测定CC细胞的增殖、侵袭、迁移和凋亡。在CC组织和细胞中观察到较高的miR-92b-3p表达水平和较低的KLF3表达水平。抑制miR-92b-3p或过表达KLF3可降低CC细胞的增殖、侵袭和迁移,同时诱导其凋亡。验证KLF3是miR-92b-3p的靶基因。敲低KLF3可逆转miR-92b-3p抑制对CC细胞的抗肿瘤作用。miR-92b-3p通过抑制KLF3促进CC的发展这可能为未来开发治疗靶点提供一种新途径。

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