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整合的miRNA谱分析和生物信息学分析揭示了胃腺癌中潜在的致病miRNA。

Integrated miRNA profiling and bioinformatics analyses reveal potential causative miRNAs in gastric adenocarcinoma.

作者信息

Zhang Xiaojing, Peng Yin, Jin Zhe, Huang Weiling, Cheng Yulan, Liu Yudan, Feng Xianling, Yang Mengting, Huang Yong, Zhao Zhenfu, Wang Liang, Wei Yanjie, Fan Xinmin, Zheng Duo, Meltzer Stephen J

机构信息

Department of Pathology, The Shenzhen University School of Medicine, Shenzhen, Guangdong, People's Republic of China.

Shenzhen Key Laboratory of Translational Medicine of Tumor, The Shenzhen University School of Medicine, Shenzhen, Guangdong, People's Republic of China.

出版信息

Oncotarget. 2015 Oct 20;6(32):32878-89. doi: 10.18632/oncotarget.5419.

Abstract

Gastric cancer (GC) is one of the leading causes of cancer-related deaths throughout China and worldwide. The discovery of microRNAs (miRNAs) has provided a new opportunity for developing diagnostic biomarkers and effective therapeutic targets in GC. By performing microarray analyses of benign and malignant gastric epithelial cell lines (HFE145, NCI-N87, MKN28, RF1, KATO III and RF48), 16 significantly dysregulated miRNAs were found. 11 of these were validated by real-time qRT-PCR. Based on miRWalk online database scans, 703 potential mRNA targets of the 16 miRNAs were identified. Bioinformatic analyses suggested that these dysregulated miRNAs and their predicted targets were principally involved in tumor pathogenesis, MAPK signaling, and apoptosis. Finally, miRNA-gene network analyses identified miRNA-125b as a crucial miRNA in GC development. Taken together, these results develop a comprehensive expression and functional profile of differentially expressed miRNAs related to gastric oncogenesis. This profile may serve as a potential tool for biomarker and therapeutic target identification in GC patients.

摘要

胃癌(GC)是中国乃至全球癌症相关死亡的主要原因之一。微小RNA(miRNA)的发现为开发胃癌诊断生物标志物和有效的治疗靶点提供了新的契机。通过对良性和恶性胃上皮细胞系(HFE145、NCI-N87、MKN28、RF1、KATO III和RF48)进行微阵列分析,发现了16种显著失调的miRNA。其中11种通过实时定量逆转录聚合酶链反应(qRT-PCR)得到验证。基于miRWalk在线数据库扫描,鉴定出这16种miRNA的703个潜在mRNA靶点。生物信息学分析表明,这些失调的miRNA及其预测靶点主要参与肿瘤发病机制、丝裂原活化蛋白激酶(MAPK)信号传导和细胞凋亡。最后,miRNA-基因网络分析确定miRNA-125b是胃癌发生发展中的关键miRNA。综上所述,这些结果揭示了与胃癌发生相关的差异表达miRNA的综合表达和功能概况。这一概况可能成为胃癌患者生物标志物和治疗靶点鉴定的潜在工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e054/4741736/33983dab6384/oncotarget-06-32878-g001.jpg

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