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LncRNA-NEAT1 inhibits the occurrence and development of pancreatic cancer through spongy miR-146b-5p/traf6.长链非编码RNA-NEAT1通过海绵吸附微小RNA-146b-5p/肿瘤坏死因子受体相关因子6抑制胰腺癌的发生和发展。
Biotechnol Genet Eng Rev. 2024 Oct;40(2):1094-1112. doi: 10.1080/02648725.2023.2192059. Epub 2023 Mar 23.
3
Colorectal cancer statistics, 2023.2023 年结直肠癌统计数据。
CA Cancer J Clin. 2023 May-Jun;73(3):233-254. doi: 10.3322/caac.21772. Epub 2023 Mar 1.
4
Cancer statistics, 2023.癌症统计数据,2023 年。
CA Cancer J Clin. 2023 Jan;73(1):17-48. doi: 10.3322/caac.21763.
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miR-125b-5p upregulation by TRIM28 induces cisplatin resistance in non-small cell lung cancer through CREB1 inhibition.miR-125b-5p 通过 TRIM28 的上调诱导非小细胞肺癌对顺铂耐药,通过 CREB1 抑制。
BMC Pulm Med. 2022 Dec 7;22(1):469. doi: 10.1186/s12890-022-02272-9.
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Mechanism of Resveratrol-Induced Programmed Cell Death and New Drug Discovery against Cancer: A Review.白藜芦醇诱导程序性细胞死亡的机制及抗癌新药研发:综述
Int J Mol Sci. 2022 Nov 8;23(22):13689. doi: 10.3390/ijms232213689.
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Mol Biotechnol. 2023 Jun;65(6):961-969. doi: 10.1007/s12033-022-00601-1. Epub 2022 Nov 15.
8
Resveratrol inhibits proliferation and induces apoptosis via the Hippo/YAP pathway in human colon cancer cells.白藜芦醇通过 Hippo/YAP 通路抑制人结肠癌细胞增殖并诱导其凋亡。
Biochem Biophys Res Commun. 2022 Dec 25;636(Pt 1):197-204. doi: 10.1016/j.bbrc.2022.10.077. Epub 2022 Oct 25.
9
Resveratrol Induces Autophagy and Apoptosis in Non-Small-Cell Lung Cancer Cells by Activating the NGFR-AMPK-mTOR Pathway.白藜芦醇通过激活 NGFR-AMPK-mTOR 通路诱导非小细胞肺癌细胞自噬和凋亡。
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MIR4435-2HG, miR-125b-5p, and Sema4D axis affects the aggressiveness of colorectal cancer cells.MIR4435-2HG、miR-125b-5p 和 Sema4D 轴影响结直肠癌细胞的侵袭性。
Folia Histochem Cytobiol. 2022;60(2):191-202. doi: 10.5603/FHC.a2022.0018. Epub 2022 Jun 22.

白藜芦醇通过调节miR-125b-5p/TRAF6信号轴抑制结直肠癌转移。

Resveratrol restrains colorectal cancer metastasis by regulating miR-125b-5p/TRAF6 signaling axis.

作者信息

Gao Xin, Zhu Ying, Lv Tongdan, Luo Mingpeng, Jiang Yu, Sun Leitao, Zheng Shusen, Jiang Donghai, Ruan Shanming

机构信息

The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Chinese Medicine) Hangzhou 310006, Zhejiang, China.

NHC Key Laboratory of Combined Multi-Organ Transplantation Hangzhou 310003, Zhejiang, China.

出版信息

Am J Cancer Res. 2024 May 15;14(5):2390-2407. doi: 10.62347/ZBVG9125. eCollection 2024.

DOI:10.62347/ZBVG9125
PMID:38859844
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11162648/
Abstract

Colorectal cancer is one of the most common malignancies with a high incidence, metastatic tendency and low 5-year survival rate. Resveratrol, a polyphenolic compound has been shown to inhibit colorectal cancer metastasis in recent studies. Its underlying molecular mechanism remains to be elucidated. Our findings demonstrated that miR-125b-5p, acting as a tumor suppressor, was conspicuously down-regulated in both colorectal cancer tissues and cell lines. The expression of miR-125b-5p negatively correlated with the expression of its direct target TNF receptor associated factor 6 (TRAF6). Both miR-125b-5p overexpression and TRAF6 knockdown inhibited metastasis of colorectal cancer cells. In addition, we uncovered that resveratrol up-regulated miR-125b-5p by increasing its stability and suppressed TRAF6-induced signal pathway in a dose/time-dependent manner. Resveratrol could significantly curtail the migration and invasion of colorectal cancer cells, which was counteracted by miR-125b-5p knockdown or TRAF6 overexpression. These results indicated that resveratrol could restrain colorectal cancer metastasis by promoting miR-125b-5p/TRAF6 signaling axis. Furthermore, lung metastasis models of colorectal cancer were constructed by tail vein injection. Down-regulation of miR-125b-5p could facilitate colorectal cancer metastasis in vivo, which could be impeded by resveratrol. In conclusion, our findings delineated the miR-125b-5p/TRAF6 signaling axis as a novel molecular mechanism underlying the metastatic process in colorectal cancer, as well as a prospective therapeutic target. Resveratrol disrupts colorectal cancer metastasis by activating miR-125b-5p/TRAF6 signal pathway and might improve the clinical outcome of colorectal cancer patients with low expression of miR-125b-5p.

摘要

结直肠癌是最常见的恶性肿瘤之一,具有高发病率、转移倾向和低5年生存率。白藜芦醇是一种多酚类化合物,最近的研究表明它能抑制结直肠癌转移。其潜在的分子机制仍有待阐明。我们的研究结果表明,作为一种肿瘤抑制因子的miR-125b-5p在结直肠癌组织和细胞系中均显著下调。miR-125b-5p的表达与其直接靶点肿瘤坏死因子受体相关因子6(TRAF6)的表达呈负相关。miR-125b-5p过表达和TRAF6敲低均抑制结直肠癌细胞的转移。此外,我们发现白藜芦醇通过增加miR-125b-5p的稳定性上调其表达,并以剂量/时间依赖性方式抑制TRAF6诱导的信号通路。白藜芦醇可显著抑制结直肠癌细胞的迁移和侵袭,而miR-125b-5p敲低或TRAF6过表达可抵消这种作用。这些结果表明,白藜芦醇可通过促进miR-125b-5p/TRAF6信号轴抑制结直肠癌转移。此外,通过尾静脉注射构建了结直肠癌肺转移模型。miR-125b-5p的下调可促进结直肠癌在体内的转移,而白藜芦醇可抑制这种转移。总之,我们的研究结果阐明了miR-125b-5p/TRAF6信号轴是结直肠癌转移过程中的一种新的分子机制,也是一个有前景的治疗靶点。白藜芦醇通过激活miR-125b-5p/TRAF6信号通路破坏结直肠癌转移,可能改善miR-125b-5p低表达的结直肠癌患者的临床结局。