MiR-145-5p在大肠癌中的表达及与多药耐药的关系  被引量:3

Expression of miR-145-5p in colorectal cancer and its relationship with multidrug resistance

在线阅读下载全文

作  者:袁亚男 杜梦楠[1] 严晓丽[1] 黄艳洁 郑纪宁[1] YUAN Ya-nan;DU Meng-nan;YAN Xiao-li;HUANG Yan-jie;ZHENG Ji-ning(Department of Pathology and Pathophysiology,Chengde Medical University,Hebei Chengde 067000,China)

机构地区:[1]承德医学院病理学与病理生理学教研室,河北承德067000

出  处:《解剖学报》2020年第4期553-556,共4页Acta Anatomica Sinica

基  金:承德医学院自然科学研究计划项目(201707);河北省高校省级重点学科建设项目(冀教高〔2013〕4号病理学与病理生理学)。

摘  要:目的探讨大肠癌中miR-145-5p和多药耐药基因(MDR1)蛋白P-糖蛋白(P-gp)的表达及两者的关系。方法分别在组织、细胞水平采用SP法、Real-time PCR法、Western blotting法检测50例大肠癌(CRC)患者组织及30例癌旁正常组织患者中P-gp的表达,miR-145-5p的表达变化对MDR1 mRNA及P-gp的影响及两者与临床病理特征之间的相关性。结果大肠癌组织中miR-145-5p表达量明显低于癌旁正常组织,MDR1 mRNA及P-gp的表达量明显高于癌旁正常组织(r=-0.403,P<0.01)。大肠癌细胞(HCT-15)中miR-145-5p能够抑制MDR1 mRNA及P-gp的表达(P<0.05)。结论MiR-145-5p对大肠癌多药耐药基因及蛋白的表达具有调控作用,参与了大肠癌的发生、发展及多药耐药。Objective To investigate the expression and relationship between miR-145-5 p and multidrug resistance gene(MDR1)protein P-glycoprotein(P-gp)in colorectal cancer.Methods SP,Real-time PCR and Western blotting were used to detect the expression of P-gp colorectal carcinoma(CRC)in 50 patients and in 30 paracancerous normal tissue patients,the effect of miR-145-5 p expression on MDR1 mRNA and P-gp and the correlation between them and clinicopathological features.Results The expression level of miR-145-5 p in CRC was significantly lower than that in paracancerous normal tissue,and the expression level of MDR1 mRNA and P-gp was significantly higher than that in paracancerous normal tissue(r=-0.403,P<0.01).MiR-145-5 p could inhibit the expression of MDR1 mRNA and P-gp in HCT-15 cells(P<0.05).Conclusion MiR-145-5 p plays a regulatory role in the expression of multidrug resistance genes and proteins in colorectal cancer,and is involved in the occurrence,development and multidrug resistance of colorectal cancer.

关 键 词:大肠癌 MiR-145-5p P-糖蛋白 多药耐药 免疫组织化学 实时定量聚合酶连反应 免疫印迹法  

分 类 号:R73[医药卫生—肿瘤]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象