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微小RNA-942通过激活Wnt/β-连环蛋白信号通路促进食管鳞状细胞癌中癌症干细胞样特性。

miR-942 promotes cancer stem cell-like traits in esophageal squamous cell carcinoma through activation of Wnt/β-catenin signalling pathway.

作者信息

Ge Chunlei, Wu Shikai, Wang Weiwei, Liu Zhimin, Zhang Jianhua, Wang Zhenyu, Li Ruilei, Zhang Zhiwei, Li Zhen, Dong Suwei, Wang Ying, Xue Yuanbo, Yang Jinyan, Tan Qinghua, Wang Ziping, Song Xin

机构信息

Department of Cancer Biotherapy Center, The Third Affiliated Hospital of Kunming Medical University (Tumor Hospital of Yunnan Province), Kunming, Yunnan, People's Republic of China.

Department of Radiation Oncology, Affiliated Hospital of Academy of Military Medical Sciences, Beijing, People's Republic of China.

出版信息

Oncotarget. 2015 May 10;6(13):10964-77. doi: 10.18632/oncotarget.3696.

Abstract

The Wnt/β-catenin signalling pathway is known to play a vital role in the maintenance of cancer stem cells (CSCs), which are reported to be the origin of malignant cancers, and result in poor prognosis of multiple kinds of cancer. Therefore, it is of great importance to illuminate the mechanism by which the Wnt/β-catenin pathway regulates the cancer stem cell-like traits in cancers. Here, we report that miR-942 is significantly upregulated in esophageal squamous cell carcinoma (ESCC), and miR-942 levels are associated with poor prognosis in ESCC patients. Overexpression of miR-942 promotes, whereas inhibition of miR-942 decreases, the tumor sphere formation, the CD90+ subpopulation cells and the expression of pluripotency associated markers. Moreover, in vivo assay shows that miR-942 overexpressing cells form larger tumors and display higher tumourigenesis. Furthermore, we demonstrate that miR-942 upregulates the Wnt/β-catenin signaling activity via directly targeting sFRP4, GSK3β and TLE1, which are multiple level negative regulators of the Wnt/β-catenin signaling cascade. In addition, our results indicate that c-myc directly binds to the miR-942 promoter and promotes its expression. Taken together, our findings establish an oncogenic role of miR-942 in ESCC and indicate that miR-942 might be an effective therapeutic target for ESCC.

摘要

已知Wnt/β-连环蛋白信号通路在癌症干细胞(CSCs)的维持中起着至关重要的作用,据报道癌症干细胞是恶性肿瘤的起源,并导致多种癌症的预后不良。因此,阐明Wnt/β-连环蛋白通路调节癌症中癌症干细胞样特性的机制非常重要。在此,我们报道miR-942在食管鳞状细胞癌(ESCC)中显著上调,且miR-942水平与ESCC患者的不良预后相关。miR-942的过表达促进肿瘤球形成、CD90+亚群细胞以及多能性相关标志物的表达,而抑制miR-942则会使其降低。此外,体内实验表明,过表达miR-942的细胞形成更大的肿瘤并显示出更高的肿瘤发生能力。此外,我们证明miR-942通过直接靶向sFRP4、GSK3β和TLE1上调Wnt/β-连环蛋白信号活性,这三者是Wnt/β-连环蛋白信号级联的多级负调节因子。另外,我们的结果表明c-myc直接结合到miR-942启动子并促进其表达。综上所述,我们的研究结果确立了miR-942在ESCC中的致癌作用,并表明miR-942可能是ESCC的有效治疗靶点。

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