标题:Genome-wide transcriptional analysis of BRD4-regulated genes and pathways in human glioma U251 cells
作者:Du, Zhanhui; Song, Xiuxiang; Yan, Fangfang; Wang, Jingjing; Zhao, Yuxia; Liu, Shangming
作者机构:[Du, Zhanhui; Liu, Shangming] Shandong Univ, Chinese Minist Educ, Key Lab Cardiovasc Remodelling & Funct Res, Qilu Hosp, Jinan 250012, Shandong, Peopl 更多
通讯作者:Zhao, YX;Liu, SM
通讯作者地址:[Zhao, YX]Shandong Univ, Qilu Hosp, Dept Tradit Chinese Med, 107 Wenhua Xi Rd, Jinan 250012, Shandong, Peoples R China;[Liu, SM]Shandong Univ, Dept Hi 更多
来源:INTERNATIONAL JOURNAL OF ONCOLOGY
出版年:2018
卷:52
期:5
页码:1415-1426
DOI:10.3892/ijo.2018.4324
关键词:bromodomain containing 4; human glioma; proliferation; apoptosis;; transcriptional analysis; KRAS proto-oncogene GTPase
摘要:Bromodomain containing 4 (BRD4), a member of the bromodomain and extra-terminal family, has become a promising drug target for numerous types of cancer. BRD4 has been reported to be deregulated in gliomas; however, the precise molecular pathways regulated by BRD4 remained elusive. In the present study, BRD4 expression was silenced in the glioma cell line U251 and the results demonstrated that BRD4 knockdown attenuated cell proliferation and promoted cell apoptosis. A genome-wide analysis of BRD4-regulated transcripts in U251 cells was performed using microarray to reveal the possible molecular mechanism. A total of 3,529 differentially expressed genes were identified; 1,648 of these genes were upregulated and 1,881 were downregulated. The results of the gene ontology analysis revealed that these genes were mainly involved in membrane organization, mitotic cell cycle, cell division and DNA replication. Pathway analysis revealed that the pathways altered following BRD4 knockdown included multiple cellular processes, such as cell cycle and apoptosis. Candidate genes were identified through global signal transduction network analysis and were validated using reverse transcription-quantitative polymerase chain reaction and western blot analyses. The results demonstrated that BRD4 knockdown decreased the expression of KRAS proto-oncogene GTPase (KRAS). Downregulated KRAS expression in U251 cells restrained cell proliferation and promoted cell apoptosis, suggesting that the effect of BRD4 on glioma cells might occur through the Ras pathway. In conclusion, the present results confirmed the role of BRD4 in glioma and provided information for further exploration of the molecular mechanism of BRD4 in glioma development and progression.
收录类别:SCOPUS;SCIE
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85044398500&doi=10.3892%2fijo.2018.4324&partnerID=40&md5=ca7b5712239a0f13da56812580be3d44
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