Department of Gastrointestinal Surgery, Nanjing Drum Tower Hospital, the Affiliated Hospital of Nanjing University Medical School, Nanjing 210008, Jiangsu Province, China.
Department of Gastrointestinal Surgery, Nanjing Drum Tower Hospital, the Affiliated Hospital of Nanjing University Medical School, Nanjing 210008, Jiangsu Province, China.
Arab J Gastroenterol. 2024 Feb;25(1):42-50. doi: 10.1016/j.ajg.2023.11.005. Epub 2024 Jan 13.
MicroRNA (miRNA) is involved in diverse biological and physiological processes of tumors. Dysregulation of miRNA will induce a series of human diseases. miR-129-2-3p has vital effects in the pathogenesis of various tumors. However, the regulatory function of miR-129-2-3p in colon cancer remains to be clarified. This study investigated the role of miR-129-2-3p targeting BZW1 in proliferation, apoptosis, migration, and invasion of colon cancer.
Here, RT-qPCR was applied to measure the miR-129-2-3p levels in colon cancer tissues. The predicted targets of miR-129-2-3p were identified by bioinformatics and verified using luciferase reporter assay. The effects of miR-129-2-3p on colon cancer were detected by CCK-8, colony formation, transwell chamber test, wound healing, and flow cytometry assays. Finally, the influence of miR-129-2-3p on tumor growth was studied. Nude mice were xenografted with transfected Lovo cells by subcutaneous injection of 5 × 10 cells in 100 µl. HE staining and TUNEL were used to assess metastasis ability.
miR-129-2-3p level in colon cancer tissue was significantly reduced. Furthermore, it was verified that BZW1 was a target of miR-129-2-3p, and its expression in colon cancer cells was inhibited by miR-129-2-3p. Additionally, miR-129-2-3p inhibited colon cancer cell proliferation, colony formation, mobility ability and tumor growth, and promoted cell apoptosis by targeting BZW1. miR-129-2-3p overexpression in tumor xenografts in vivo decreased BZW1 expression, and suppressed tumor growth.
Collectively, these findings indicated that miR-129-2-3p exerts a suppressive role in colon cancer cells by directly targeting BZW1, and may have significant therapeutic implications for patients with colon cancer.
微小 RNA(miRNA)参与肿瘤的多种生物学和生理过程。miRNA 的失调会导致一系列人类疾病。miR-129-2-3p 在各种肿瘤的发病机制中具有重要作用。然而,miR-129-2-3p 对结肠癌的调控作用仍有待阐明。本研究探讨了 miR-129-2-3p 靶向 BZW1 对结肠癌增殖、凋亡、迁移和侵袭的调节作用。
本研究采用 RT-qPCR 测定结肠癌组织中 miR-129-2-3p 的水平。通过生物信息学预测 miR-129-2-3p 的靶标,并通过荧光素酶报告基因实验进行验证。通过 CCK-8、集落形成、Transwell 室试验、划痕愈合和流式细胞术检测 miR-129-2-3p 对结肠癌的影响。最后,研究了 miR-129-2-3p 对肿瘤生长的影响。通过皮下注射 100μl 含 5×10 个转染 Lovo 细胞的方式,在裸鼠中进行转染细胞的异种移植。使用 HE 染色和 TUNEL 评估转移能力。
结肠癌组织中 miR-129-2-3p 的水平显著降低。此外,验证了 BZW1 是 miR-129-2-3p 的靶标,miR-129-2-3p 可抑制结肠癌细胞中的 BZW1 表达。此外,miR-129-2-3p 通过靶向 BZW1 抑制结肠癌细胞增殖、集落形成、迁移能力和肿瘤生长,并促进细胞凋亡。体内肿瘤异种移植中 miR-129-2-3p 的过表达降低了 BZW1 的表达,抑制了肿瘤生长。
综上所述,这些发现表明 miR-129-2-3p 通过直接靶向 BZW1 对结肠癌细胞发挥抑制作用,可能对结肠癌患者具有重要的治疗意义。