MiR-125b acts as an oncogene in glioblastoma cells and inhibits cell apoptosis through p53 and p38MAPK-independent pathways
文献类型:期刊论文
作者 | Wu, N.1; Lin, X.2; Zhao, X.3![]() |
刊名 | BRITISH JOURNAL OF CANCER
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出版日期 | 2013-11-26 |
卷号 | 109期号:11页码:2853-2863 |
关键词 | microRNA miR-125b glioblastoma cell apoptosis p53 p38MAPK |
ISSN号 | 0007-0920 |
通讯作者 | Lin, X |
中文摘要 | Background: We have recently identified miR-125b upregulation in glioblastoma (GMB). The aim of this study is to determine the correlation between miR-125b expression and malignant grades of glioma and the genes targeted by miR-125b. Methods: Real-time PCR was employed to measure the expression level of miR-125b. Cell viability was evaluated by cell growth and colony formation in soft-agar assays. Cell apoptosis was determined by Hoechst 33342 staining and AnnexinV-FITC assay. The Luciferase assay was used to confirm the actual binding sites of p38MAPK mRNA. Western blot was used to detect the gene expression level. Results: The expression level of miR-125b is positively correlated with the malignant grade of glioma. Ectopic expression of miR-125b promotes the proliferation of GMB cells. Knockdown of endogenous miR-125b inhibits cell proliferation and promotes cell apoptosis. Further studies reveal that p53 is regulated by miR-125b. However, downregulation of the endogenous miR-125b also results in p53-independent apoptotic pathway leading to apoptosis in p53 mutated U251 cells and p53 knockdown U87 cells. Moreover, p38MAPK is also regulated by miR-125b and downregulation of miR-125b activates the p38MAPK-induced mitochondria apoptotic pathway. Conclusion: High-level expression of miR-125b is associated with poor outcomes of GMB. MiR-125b may have an oncogenic role in GMB cells by promoting cell proliferation and inhibiting apoptosis. |
英文摘要 | Background: We have recently identified miR-125b upregulation in glioblastoma (GMB). The aim of this study is to determine the correlation between miR-125b expression and malignant grades of glioma and the genes targeted by miR-125b. |
WOS标题词 | Science & Technology ; Life Sciences & Biomedicine |
学科主题 | Oncology |
类目[WOS] | Oncology |
研究领域[WOS] | Oncology |
关键词[WOS] | ACTIVATED PROTEIN-KINASES ; ANTAGONIST KILLER 1 ; NEURONAL DIFFERENTIATION ; MICRORNA SIGNATURES ; OVARIAN-CANCER ; STEM-CELLS ; EXPRESSION ; CONFERS ; PROLIFERATION ; TEMOZOLOMIDE |
收录类别 | SCI |
原文出处 | 10.1038/bjc.2013.672 |
语种 | 英语 |
WOS记录号 | WOS:000327762700014 |
公开日期 | 2014-07-17 |
源URL | [http://ir.qdio.ac.cn/handle/337002/16678] ![]() |
专题 | 海洋研究所_实验海洋生物学重点实验室 |
作者单位 | 1.Chinese Acad Sci, Inst Oceanol, Qingdao 266071, Peoples R China 2.Capital Med Univ, Dept Pharmacol, Beijing 100069, Peoples R China 3.Qingdao Univ, Cent Lab, Affiliated Hosp, Coll Med, Qingdao 266003, Peoples R China 4.Chinese Acad Fishery Sci, Yellow Sea Fisheries Res Inst, Qingdao 266071, Peoples R China 5.Qingdao Agr Univ, Coll Chem & Pharmaceut Sci, Qingdao 266109, Peoples R China 6.Roswell Pk Canc Inst, Dept Med, Buffalo, NY 14263 USA |
推荐引用方式 GB/T 7714 | Wu, N.,Lin, X.,Zhao, X.,et al. MiR-125b acts as an oncogene in glioblastoma cells and inhibits cell apoptosis through p53 and p38MAPK-independent pathways[J]. BRITISH JOURNAL OF CANCER,2013,109(11):2853-2863. |
APA | Wu, N..,Lin, X..,Zhao, X..,Zheng, L..,Xiao, L..,...&Cao, S..(2013).MiR-125b acts as an oncogene in glioblastoma cells and inhibits cell apoptosis through p53 and p38MAPK-independent pathways.BRITISH JOURNAL OF CANCER,109(11),2853-2863. |
MLA | Wu, N.,et al."MiR-125b acts as an oncogene in glioblastoma cells and inhibits cell apoptosis through p53 and p38MAPK-independent pathways".BRITISH JOURNAL OF CANCER 109.11(2013):2853-2863. |
入库方式: OAI收割
来源:海洋研究所
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