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miR-130b调控RAB34的表达在胰腺癌发生发展中的作用
引用本文:何峰,陈曦,程方雄,闵小春,曹忠厚,丁锋. miR-130b调控RAB34的表达在胰腺癌发生发展中的作用[J]. 肿瘤防治研究, 2018, 45(3): 144-147. DOI: 10.3971/j.issn.1000-8578.2018.17.0960
作者姓名:何峰  陈曦  程方雄  闵小春  曹忠厚  丁锋
作者单位:1. 430077 武汉,华中科技大学同济医学院附属普爱医院检验科;2. 430064 武汉,武汉市江汉区疾病预防控制中心检验科;3. 430019 武汉,武汉市长江航务管理局疾病预防控制中心
基金项目:武汉市卫计委科研基金(WX13C15)
摘    要:目的 探讨miR-130b调控Ras相关蛋白34(Ras-related proteins in brain 34, RAB34)在胰腺癌中的表达。方法 收集22例胰腺癌及其癌旁组织标本,采用免疫组织化学、Western blot和qRT-PCR法检测RAB34的表达;qRT-PCR法检测miR-130b表达;细胞转染法检测miR-130b调控RAB34表达,双荧光素酶报告基因检测系统验证miR-130b结合RAB34的3’UTR的靶位点。结果 与癌旁组织对比,RAB34在胰腺癌组织中显著高表达,且miR-130b显著低表达;转染miR-130b mimics可抑制RAB34的表达;RAB34是miR-130b作用的靶基因。结论 RAB34是胰腺癌的分子标志物,miR-130b可调控其表达。

关 键 词:胰腺癌  RAB34  miR-130b  
收稿时间:2017-08-07

Effect of miR-130b Targeting RAB34 Expression in Occurrence and Development of Pancreatic Cancer
HE Feng,CHEN Xi,CHENG Fangxiong,MIN Xiaochun,CAO Zhonghou,DING Feng. Effect of miR-130b Targeting RAB34 Expression in Occurrence and Development of Pancreatic Cancer[J]. Cancer Research on Prevention and Treatment, 2018, 45(3): 144-147. DOI: 10.3971/j.issn.1000-8578.2018.17.0960
Authors:HE Feng  CHEN Xi  CHENG Fangxiong  MIN Xiaochun  CAO Zhonghou  DING Feng
Affiliation:1. Department of Laboratory, Puai Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430077, China; 2. Clinical Laboratory, Jianghan Center for Disease Prevention and Control in Wuhan, Wuhan 430064, China; 3. Disease Prevention and Control of Changjiang River Administration in Wuhan, Wuhan 430019, China
Abstract:Objective To investigate the expression of Ras-related proteins in brain 34 (RAB34) regulated by miR-130b in pancreatic cancer. Methods We collected 22 paired specimens of primary pancreatic cancer and adjacent normal tissues specimens. Immunohistochemistry, Western blot and qRT-PCR were employed to detect the expression level of RAB34. Meanwhile, the expression of miR-130b was detected by qRT-PCR. Cell transfection method was used to discover the regulation of miR-130b on RAB34 gene. The luciferase reporter assay was applied to identify whether RAB34 was directly targeted by miR-130b. Results Compared with adjacent tissues specimens, miR-130b was significantly downregulated and its target gene RAB34 was upregulated in pancreatic cancer tissues. Overexpression of miR-130b remarkably inhibited the expression of RAB34. Moreover, the dual luciferase assay revealed that RAB34 was directly targeted by miR-130b. Conclusion RAB34 might have a considerable potential in prognosis identification of pancreatic cancer and be regulated by miR-130b.
Keywords:Pancreatic cancer  RAB34  miR-130b  R735.9
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