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miR-150在套细胞淋巴瘤中的表达及意义
引用本文:张新伟,王芳,任秀宝,Tao Jianguo. miR-150在套细胞淋巴瘤中的表达及意义[J]. 中国肿瘤临床, 2013, 40(13): 763-766. DOI: 10.3969/j.issn.1000-8179.2013.13.004
作者姓名:张新伟  王芳  任秀宝  Tao Jianguo
作者单位:①.天津医科大学附属肿瘤医院生物治疗科,天津市肿瘤防治重点实验室(天津市300060)
摘    要:   目的   探讨套细胞淋巴瘤(mantle cell lymphoma,MCL)中miR-150的表达情况及其临床意义。   方法   通过定量RT-PCR检测29例初治MCL患者及7例正常人外周血B细胞中miR-150和c-Myc的表达水平,探索miR-150和c-Myc表达之间的关系;利用RNAi阻断MCL细胞系Mino和HBL-2中c-Myc表达后,检测miR-150的变化,确定c-Myc是否参与miR-150的表达调控;抑制P493-6细胞表达c-Myc后,观察miR-150的变化,进一步明确miR-150是否受c-Myc调节;将pre-miR-150电转HBL-2细胞系,通过集落形成试验明确miR-150对细胞增殖的影响,Western blot检测c-Myb蛋白的变化。   结果   与正常人外周血B细胞相比,MCL患者低表达miR-150、过表达c-Myc,两者的表达呈负相关;阻断c-Myc后,Mino和HBL-2细胞的miR-150表达增加;抑制c-Myc表达后,P493-6细胞的miR-150表达增高;过表达miR-150后,HBL-2的c-Myb蛋白表达水平和集落形成能力下降。   结论   MCL患者低表达miR-150的原因可能与其c-Myc过表达有关。miR-150能够抑制MCL的增殖,在MCL的治疗中具有潜在价值。 

关 键 词:套细胞淋巴瘤   miR-150   c-Myc
收稿时间:2012-11-27

MiR-150 downregulation and its significance in mantle cell lymphoma
Xinwei ZHANG , Fang WANG , Xiubao REN , Jianguo TAO. MiR-150 downregulation and its significance in mantle cell lymphoma[J]. Chinese Journal of Clinical Oncology, 2013, 40(13): 763-766. DOI: 10.3969/j.issn.1000-8179.2013.13.004
Authors:Xinwei ZHANG    Fang WANG    Xiubao REN    Jianguo TAO
Affiliation:①.Department of Biotherapy, Tianjin Medical University Cancer Institute and Hospital, Tianjin 300060, China②.Department of Malignant Hematology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL 33613, USA
Abstract:   Objective   This study explores the miR-150 expression and its clinical significance in mantle cell lymphoma (MCL).   Methods   The miR-150 and c-Myc expression was measured in 29 primary MCL tissue samples and 7 normal donors through quantitative real-time polymerase chain reaction. MiR-150 expression was detected in Mino and HBL-2 cells after c-Myc was knocked down by small interfering RNAs. MiR-150 was analyzed in tet-treated P493-6 cells with Myc turned off. The number of tumor colonies in the BL-2 cells transfected with pre-miR-150 was determined through colony formation assay, and c-Myb was detected through Western blot.   Results   Compared with the normal donors, miR-150 expression was significantly downregulated and c-Myc was considerably overexpressed in MCL. Moreover, MCLs with high Myc expression had a significantly low miR-29 expression. MiR-150 was upregulated in the Mino and HBL-2 cells with c-Myc knockdown. MiR-150 was evidently upregulated in P493-6 cells after c-Myc was turned off. MiR-150 overexpression suppressed colony formation and c-Myb expression of HBL-2.   Conclusion   MiR-150 is downregulated in MCL, which may be related to c-Myc overexpression. The recovery of miR-150 suppresses MCL cell survival. These results indicate that miR-150 may be a potential therapeutic target of MCL. 
Keywords:mantle cell lymphoma  miR-150  c-Myc
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