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脂肪量与肥胖相关基因(FTO)的下调促进肝内胆管癌的进展。

Downregulation of Fat Mass and Obesity Associated (FTO) Promotes the Progression of Intrahepatic Cholangiocarcinoma.

作者信息

Rong Zhuo-Xian, Li Zhi, He Jun-Ju, Liu Li-Yu, Ren Xin-Xin, Gao Jie, Mu Yun, Guan Yi-Di, Duan Yu-Mei, Zhang Xiu-Ping, Zhang De-Xiang, Li Nan, Deng Yue-Zhen, Sun Lun-Quan

机构信息

Center for Molecular Medicine, Xiangya Hospital, Central South University, Changsha, China.

Key Laboratory of Molecular Radiation Oncology, Changsha, China.

出版信息

Front Oncol. 2019 May 9;9:369. doi: 10.3389/fonc.2019.00369. eCollection 2019.

Abstract

Intrahepatic cholangiocarcinoma (ICC) ranks as the second most malignant type of primary liver cancer with a high degree of incidence and a very poor prognosis. Fat mass and obesity-associated protein (FTO) functions as an eraser of the RNA mA modification, but its roles in ICC tumorigenesis and development remain unknown. We showed here that the protein level of FTO was downregulated in clinical ICC samples and cell lines and that FTO expression was inversely correlated with the expression of CA19-9 and micro-vessel density (MVD). A Kaplan-Meier survival analysis showed that a low expression of predicted poor prognosis in ICC. , decreased endogenous expression of obviously reduced apoptosis of ICC cells. Moreover, suppressed the anchorage-independent growth and mobility of ICC cells. Through mining the database, FTO was found to regulate the integrin signaling pathway, inflammation signaling pathway, epidermal growth factor receptor (EGFR) signaling pathway, angiogenesis, and the pyrimidine metabolism pathway. RNA decay assay showed that oncogene mRNA stability was impaired by FTO. In addition, the overexpression of FTO suppressed tumor growth . In conclusion, our study demonstrated the critical roles of FTO in ICC.

摘要

肝内胆管癌(ICC)是原发性肝癌中恶性程度第二高的类型,发病率高且预后很差。脂肪量和肥胖相关蛋白(FTO)作为RNA mA修饰的去甲基化酶,但其在ICC发生发展中的作用尚不清楚。我们在此表明,FTO蛋白水平在临床ICC样本和细胞系中下调,且FTO表达与CA19-9表达和微血管密度(MVD)呈负相关。Kaplan-Meier生存分析表明,FTO低表达预示ICC预后不良。此外,FTO内源性表达降低明显减少了ICC细胞的凋亡。而且,FTO抑制了ICC细胞的非锚定依赖性生长和迁移能力。通过数据库挖掘发现,FTO可调节整合素信号通路、炎症信号通路、表皮生长因子受体(EGFR)信号通路、血管生成以及嘧啶代谢途径。RNA降解试验表明,FTO会损害癌基因mRNA的稳定性。此外,FTO过表达抑制肿瘤生长。总之,我们研究证明了FTO在ICC中的关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1da/6521779/153e32bd865b/fonc-09-00369-g0001.jpg

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