Cancer and Anticancer Drug Research Center, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, 325035, China.
Affiliated Hospital 1, Wenzhou Medical University, Wenzhou, Zhejiang, 325035, China.
Cell Death Dis. 2020 Sep 22;11(9):785. doi: 10.1038/s41419-020-02997-7.
Our recent study demonstrated that the QKI-5 regulated miRNA, miR-196b-5p, and it functions as an onco-microRNA in non-small cell lung cancer (NSCLC) by directly targeting GATA6 and TSPAN12. However, the role of miR-196b-5p in NSCLC progression and metastasis still remains unclear. We found that miR-196b-5p promotes lung cancer cell proliferation and colony formation by directly targeting tumor suppressor, FAS. The expression of FAS was significantly downregulated in NSCLC tissue samples and was negatively correlated with the miR-196b-5p expression. Knocking down FAS activates NFkB signaling and subsequent IL6 secretion, resulting in phosphorylation of signal transducer and activator of transcription 3 (STAT3) to promote lung cancer cell growth. Our findings indicated that miR-196b-5p might exhibit novel oncogenic function by FAS-mediated STAT3 activation in NSCLC, and suggested that targeting the miR-196b-5p/FAS/NFkB/IL6/STAT3 pathway might be a promising therapeutic strategy in treating NSCLC.
我们最近的研究表明,QKI-5 调节的 microRNA,miR-196b-5p,通过直接靶向 GATA6 和 TSPAN12,在非小细胞肺癌(NSCLC)中发挥癌基因 microRNA 的作用。然而,miR-196b-5p 在 NSCLC 进展和转移中的作用仍不清楚。我们发现 miR-196b-5p 通过直接靶向肿瘤抑制因子 FAS 促进肺癌细胞增殖和集落形成。FAS 的表达在 NSCLC 组织样本中显著下调,与 miR-196b-5p 的表达呈负相关。敲低 FAS 激活 NFkB 信号通路,随后 IL6 分泌,导致信号转导和转录激活因子 3(STAT3)磷酸化,促进肺癌细胞生长。我们的研究结果表明,miR-196b-5p 通过 FAS 介导的 STAT3 激活可能在 NSCLC 中发挥新的致癌功能,并表明靶向 miR-196b-5p/FAS/NFkB/IL6/STAT3 通路可能是治疗 NSCLC 的一种有前途的治疗策略。