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长链非编码RNA通过激活磷脂酰肌醇3-激酶/AKT信号通路促进胃癌发生。

The long non-coding RNA promotes gastric cancer by activating the phosphatidylinositol 3-kinase/AKT pathway.

作者信息

Zhang Rui, Liu Yuan, Liu Hui, Chen Wei, Fan Hui-Ning, Zhang Jing, Zhu Jin-Shui

机构信息

Department of Gastroenterology, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai 200233, China.

出版信息

Aging (Albany NY). 2019 Dec 5;11(23):10902-10922. doi: 10.18632/aging.102493.

Abstract

Long non-coding RNAs contribute to the development of human cancers. We compared the long non-coding RNA levels in gastric cancer (GC) and para-cancerous tissues in the Gene Expression Omnibus, and found that small nucleolar RNA host gene 12 () was upregulated in GC tissues. Fluorescence in situ hybridization confirmed that is overexpressed in GC tissues. We then used data from The Cancer Genome Atlas to assess the association of expression with the clinicopathological characteristics and prognosis of GC patients and found that higher expression was associated with a greater tumor invasion depth and poorer survival. , silencing suppressed GC cell proliferation, migration and invasion, but induced apoptosis and cell cycle arrest. Overexpressing had the opposite effects. In xenografted mice, knocking down reduced GC tumor growth. Taken together, cancer pathway microarray and bioinformatics analyses, RNA pulldown assays, Western blotting and immunohistochemistry revealed that induces GC tumorigenesis by activating the phosphatidylinositol 3-kinase/AKT pathway. may thus be a useful marker for predicting poor survival in GC patients.

摘要

长链非编码RNA促进人类癌症的发展。我们在基因表达综合数据库中比较了胃癌(GC)组织和癌旁组织中的长链非编码RNA水平,发现小核仁RNA宿主基因12()在GC组织中上调。荧光原位杂交证实,在GC组织中过表达。然后,我们使用来自癌症基因组图谱的数据评估表达与GC患者临床病理特征和预后的相关性,发现较高的表达与更大的肿瘤浸润深度和更差的生存率相关。沉默抑制了GC细胞的增殖、迁移和侵袭,但诱导了细胞凋亡和细胞周期停滞。过表达则产生相反的效果。在异种移植小鼠中,敲低可减少GC肿瘤的生长。综合癌症通路微阵列和生物信息学分析、RNA下拉实验、蛋白质免疫印迹和免疫组织化学结果表明,通过激活磷脂酰肌醇3激酶/AKT通路诱导GC肿瘤发生。因此,可能是预测GC患者生存不良的有用标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e64/6932881/d49ae7f54e4e/aging-11-102493-g001.jpg

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