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微小 RNA-129-5p 通过抑制高迁移率族蛋白 1 来抑制口腔鳞状细胞癌的生长和侵袭。

MicroRNA-129-5p represses the growth and aggressiveness of oral squamous cell carcinoma via suppressing HMGB1.

机构信息

Department of Prosthodontics, Qingdao Stomatology Hospital, Qingdao, Shandong, China.

出版信息

Kaohsiung J Med Sci. 2020 Jul;36(7):483-493. doi: 10.1002/kjm2.12201. Epub 2020 Mar 5.

DOI:10.1002/kjm2.12201
PMID:32133766
Abstract

Recent investigations have suggested that microRNA-129-5p (miR-129-5p) is commonly dysregulated in multiple types of malignancies. Nevertheless, the roles of miR-129-5p in human oral squamous cell carcinoma (OSCC) are not well explored. Herein, we demonstrated that miR-129-5p was down-expressed in OSCC cells and tissues. Moreover, miR-129-5p overexpression restrained the growth, migration ability, and invasiveness of OSCC cells. Notably, high-mobility group box 1 protein (HMGB1) was identified as a downstream target of miR-129-5p. Additional, knockdown of HMGB1 suppressed the growth and aggressive phenotypes of human OSCC cells. Importantly, re-expression of HMGB1 impaired the inhibitory impacts of miR-129-5p on the metastasis of OSCC cells. Altogether, these results implied that miR-129-5p restrained the aggressiveness of OSCC cells through modulating HMGB1.

摘要

最近的研究表明,微小 RNA-129-5p(miR-129-5p)在多种恶性肿瘤中普遍失调。然而,miR-129-5p 在人口腔鳞状细胞癌(OSCC)中的作用尚未得到充分探索。在此,我们证明 miR-129-5p 在 OSCC 细胞和组织中表达下调。此外,miR-129-5p 的过表达抑制了 OSCC 细胞的生长、迁移能力和侵袭性。值得注意的是,高迁移率族蛋白 B1(HMGB1)被鉴定为 miR-129-5p 的下游靶标。此外,HMGB1 的敲低抑制了人 OSCC 细胞的生长和侵袭表型。重要的是,HMGB1 的重新表达削弱了 miR-129-5p 对 OSCC 细胞转移的抑制作用。总之,这些结果表明,miR-129-5p 通过调节 HMGB1 抑制 OSCC 细胞的侵袭性。

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本文引用的文献

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MiR-34c acts as a tumor suppressor in non-small cell lung cancer by inducing endoplasmic reticulum stress through targeting HMGB1.微小RNA-34c通过靶向高迁移率族蛋白B1诱导内质网应激,从而在非小细胞肺癌中发挥肿瘤抑制作用。
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miR-129-5p attenuates cell proliferation and epithelial mesenchymal transition via HMGB1 in gastric cancer.miR-129-5p通过高迁移率族蛋白B1(HMGB1)抑制胃癌细胞增殖和上皮间质转化。
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MiR-129-5p functions as a tumor suppressor in gastric cancer progression through targeting ADAM9.miR-129-5p 通过靶向 ADAM9 在胃癌进展中发挥肿瘤抑制作用。
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High mobility group box 1 promotes the epithelial-to-mesenchymal transition in prostate cancer PC3 cells via the RAGE/NF-κB signaling pathway.高迁移率族蛋白 B1 通过 RAGE/NF-κB 信号通路促进前列腺癌细胞 PC3 的上皮间质转化。
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