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作 者:段克才 陈天天 丁勇兴[1] DUAN Ke-cai;CHEN Tian-tian;DING Yong-xing(Department of General Oncology,The Third People's Hospital of Bengbu,Bengbu Anhui 233000;Clinical Testing and Diagnose Experimental Center,Bengbu Medical College,Bengbu Anhui 233030,China)
机构地区:[1]安徽省蚌埠市第三人民医院普外肿瘤科,233000 [2]蚌埠医学院临床检验诊断学实验中心,安徽蚌埠233030
出 处:《蚌埠医学院学报》2018年第11期1401-1404,共4页Journal of Bengbu Medical College
基 金:安徽省教育厅自然科学研究重大项目(KJ2015ZD29;KJ2016SD37);安徽省自然科学基金项目(1508085MH159);安徽省高校学科(专业)拔尖人才学术资助重点项目(gxbjZD2016069);安徽省蚌埠市科技计划项目(20150309)
摘 要:目的:阐明病毒巨噬细胞炎性蛋白Ⅱ(virus macrophage inflammatory protein-Ⅱ,v MIP-Ⅱ) N末端21个氨基酸的多肽(NT21MP)对乳腺癌MCF-7细胞miRNAs表达谱的调控作用。方法:收集各组细胞抽提RNA,RNA质量评估后逆转录成c DNA。采用染料法(SYBR GreenⅠ)进行相对定量分析,实验按照2-△△Ct解析法进行设计。结果:总共检测了168个miRNAs,以上调> 2倍或下调<0. 5倍筛选。相对于S组,N组升高的有9个:miR-223、miR-451a、miR-128、miR-489、miR-141、miR-320a、miR-155-3p、miR-335、miR-320e,降低的有2个:miR-15a、miR-339。结论:筛选得到NT21MP调控miRNAs差异表达谱,其为研究miRNAs在NT21MP调控中的作用机制提供依据。Objective: To investigate the effects of virus macrophage inflammatory protein-Ⅱ( v MIP-Ⅱ) N-terminal 21 amino acids peptide( NT21 MP) on the expression profiles of miRNAs in breast cancer MCF-7 cell. Methods: The RNA in each group cells was extracted,and transcribed into c DNA. The experiment was designed according to the 2^-△△Ctanalytical method,and the miRNA expression profile was analyzed using the quantitative analysis of SYBR Green I. Results: A total of 168 miRNAs genes were detected,and the genes of expression upregulating two-fold or downregulating 0. 5-fold were screened. Compared with the S group,the expression levels of miR-223-3 p,miR-451 a,miR-128,miR-489,miR-141-3 p,miR-320 a,miR-155-3 p,miR-335-3 p and miR-320 e increased,and the expression levels of miR-15 a-5 p and miR-339-5 p decreased in N group. Conclusions: The differential expression profiles of miRNAs regulated by NT21 MP were screened to provide a basis for studyiny the mechanism of miRNAs in th regulation of NT21 MP.
关 键 词:乳腺肿瘤 病毒巨噬细胞炎性蛋白Ⅱ N末端21个氨基酸多肽 MIRNAS
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