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全反式维甲酸对大肠癌细胞间隙连接蛋白Cx32与Cx43表达及增殖和迁移能力的影响
引用本文:孟令俊,卢振霞,孙步彤,白鹭鹭,石张镇,代恩勇.全反式维甲酸对大肠癌细胞间隙连接蛋白Cx32与Cx43表达及增殖和迁移能力的影响[J].吉林大学学报(医学版),2011,37(6):994-997.
作者姓名:孟令俊  卢振霞  孙步彤  白鹭鹭  石张镇  代恩勇
作者单位:吉林大学中日联谊医院肿瘤 血液科,吉林长春,130033;吉林大学第一医院儿科,吉林长春,130021
基金项目:国家自然科学基金面上项目资助课题(30870355);吉林省科技厅科技发展计划项目资助课题(200705286);吉林省长春市科委基金资助课题(2008077)
摘    要:目的:检测全反式维甲酸(ATRA)对大肠癌细胞Caco-2及SW480增殖、迁移及间隙连接蛋白Cx32与Cx43胞膜表达的影响,分析其对大肠癌效应作用机制.方法:取对数生长期大肠癌细胞分为ATRA处理组及阴性对照组,以1×10-8、1×10-7、1×10-6、1×10-5及1×10-4 mol·L-1 ATRA处理Ca...

关 键 词:大肠癌细胞  全反式维甲酸  间隙连接蛋白Cx32  间隙连接蛋白Cx43
收稿时间:2011-08-15

Effects of ATRA on Cx32 and Cx43 expressions and proliferation and migration abilities of colorectal cancer cells
MENG Ling-jun,LU Zhen-xia,SUN Bu-tong,BAI Lu-lu,SHI Zhang-zhen,DAI En-yong.Effects of ATRA on Cx32 and Cx43 expressions and proliferation and migration abilities of colorectal cancer cells[J].Journal of Jilin University: Med Ed,2011,37(6):994-997.
Authors:MENG Ling-jun  LU Zhen-xia  SUN Bu-tong  BAI Lu-lu  SHI Zhang-zhen  DAI En-yong
Institution:(1.Department of Tumor and Hematology,China-Japan Union Hospital,Jilin University,Changchun 130033,China;2.Department of Pediatrics,First Hospital,Jilin University,Changchun 130021,China)
Abstract:Objective To investigate the effects of ATRA on the proliferation and migration abilities and membranous distribution of Cx32 and Cx43 of colorectal cancer cells Caco-2 and SW480 and to elucidate the potential mechanism.Methods The colorectal cancer cell lines Caco-2 and SW480 were divided into ATRA treatment groups and control groups.The Caco-2 and SW480 cells were treated with 1×10-8,1×10-7,1×10-6,1×10-5 and 1×10-4 mol·L-1 ATRA,and MTT assay was applied to detect the inhibitory rates of growth of Caco-2 and SW480 cells.After the SW480 cells were treated with the 1×10-5 and 1×10-4 mol·L-1 ATRA,the wound healing assay was employed to determine the cell migration ability and flow cytometry was used to analyze membranous distribution of Cx 32 and Cx 43 in SW480 cells.Results Compared with control group,the growth inhibitory rates of Caco-2 and SW480 cells in ATRA groups after treated with 1×10-4 mol·L-1 for 24,48 and 72 h were significantly increased(P<0.01);the migration abilities of SW480 cells were dramatically decreased after treated with 1×10-5 mol·L-1 ATRA for 24 and 48 h(P<0.05);the membranous distribution of Cx 32 and Cx 43 of SW480 cells was remarkably increased after treated with 1×10-5 and 1×10-4 mol·L-1 ATRA for 24 and 48 h(P<0.05).Conclusion ATRA could increase the membranous distribution of Cx32 and Cx43 of colorectal cancer cells and inhibit the proliferation and migration abilities,which may be involved in the interaction between connexins and cytoplasmic proteins,as well as alteration of gap junctional intercellular communication.
Keywords:colorectal cancer cells  all-trans retinoic acid  connexin 32  connexin 43
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