Effects of Gene Tranfection with CH50 Polypeptide on the Invasion Ability of Bladder Cancer Cell Line BIU-87

The expression of CH50 polypoptide in bladder cancer cell line BIU 87 and the effects on the invasion ability of BIU 87 were investigated. The cukaryotie expressing vector pCH510 of polypeptide CH50 was introduced into BIU-87 cells by gene transfeetion in vitro. The expression of CH50 polypeptide wa...

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Veröffentlicht in:Current medical science 2005, Vol.25 (3), p.320-322
1. Verfasser: 伍庄 陈忠 叶章群 张健华 叶仕桥 张桂梅 冯作化
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description The expression of CH50 polypoptide in bladder cancer cell line BIU 87 and the effects on the invasion ability of BIU 87 were investigated. The cukaryotie expressing vector pCH510 of polypeptide CH50 was introduced into BIU-87 cells by gene transfeetion in vitro. The expression of CH50 polypeptide was detected by using immunohistoehemieal S P method. The expression of the transfeeted gene was identified by RT PCR. Cell invasion assay kit was applied to detect the effect of CH50 polypeptide on the invasion ability of BIU-87. The results showed that the BIU-87 cells transfeeted with pCH510 could express the CH50 polypeptide, while in the control group, no CH50 polypeptide was detectable. In the transfection group, the invasion ability of BIU-87 in vitro was lower than in control group (P
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The cukaryotie expressing vector pCH510 of polypeptide CH50 was introduced into BIU-87 cells by gene transfeetion in vitro. The expression of CH50 polypeptide was detected by using immunohistoehemieal S P method. The expression of the transfeeted gene was identified by RT PCR. Cell invasion assay kit was applied to detect the effect of CH50 polypeptide on the invasion ability of BIU-87. The results showed that the BIU-87 cells transfeeted with pCH510 could express the CH50 polypeptide, while in the control group, no CH50 polypeptide was detectable. In the transfection group, the invasion ability of BIU-87 in vitro was lower than in control group (P&lt;0.05). It was concluded that CH50 polypeptide was successfully expressed in BIU 87 cells by gene transfeetion, by which the in vitro invasion ability of BIU-87 was inhibited。</description><identifier>ISSN: 1672-0733</identifier><identifier>ISSN: 2096-5230</identifier><identifier>EISSN: 1993-1352</identifier><identifier>EISSN: 2523-899X</identifier><identifier>DOI: 10.1007/bf02828155</identifier><identifier>PMID: 16201284</identifier><language>eng</language><publisher>China: Department of Urology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China%Department of Pathophysiology, School of Medical Science, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China%Department of Biochemistry and Biology, School of Basic Medical Sciences, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China</publisher><subject>BIU-87 ; Cell Line, Transformed ; CH50 ; Escherichia coli - genetics ; Escherichia coli - metabolism ; Eukaryotic Cells - metabolism ; Fibronectins - biosynthesis ; Fibronectins - genetics ; Genetic Vectors ; Humans ; Neoplasm Invasiveness ; Plasmids - genetics ; Recombinant Proteins - biosynthesis ; Recombinant Proteins - genetics ; Transfection ; Urinary Bladder Neoplasms - genetics ; Urinary Bladder Neoplasms - pathology ; 基因多肽 ; 基因转化 ; 肿瘤入侵 ; 膀胱肿瘤</subject><ispartof>Current medical science, 2005, Vol.25 (3), p.320-322</ispartof><rights>Copyright © Wanfang Data Co. 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The cukaryotie expressing vector pCH510 of polypeptide CH50 was introduced into BIU-87 cells by gene transfeetion in vitro. The expression of CH50 polypeptide was detected by using immunohistoehemieal S P method. The expression of the transfeeted gene was identified by RT PCR. Cell invasion assay kit was applied to detect the effect of CH50 polypeptide on the invasion ability of BIU-87. The results showed that the BIU-87 cells transfeeted with pCH510 could express the CH50 polypeptide, while in the control group, no CH50 polypeptide was detectable. In the transfection group, the invasion ability of BIU-87 in vitro was lower than in control group (P&lt;0.05). 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The cukaryotie expressing vector pCH510 of polypeptide CH50 was introduced into BIU-87 cells by gene transfeetion in vitro. The expression of CH50 polypeptide was detected by using immunohistoehemieal S P method. The expression of the transfeeted gene was identified by RT PCR. Cell invasion assay kit was applied to detect the effect of CH50 polypeptide on the invasion ability of BIU-87. The results showed that the BIU-87 cells transfeeted with pCH510 could express the CH50 polypeptide, while in the control group, no CH50 polypeptide was detectable. In the transfection group, the invasion ability of BIU-87 in vitro was lower than in control group (P&lt;0.05). 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identifier ISSN: 1672-0733
ispartof Current medical science, 2005, Vol.25 (3), p.320-322
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language eng
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source MEDLINE; SpringerNature Journals; Alma/SFX Local Collection
subjects BIU-87
Cell Line, Transformed
CH50
Escherichia coli - genetics
Escherichia coli - metabolism
Eukaryotic Cells - metabolism
Fibronectins - biosynthesis
Fibronectins - genetics
Genetic Vectors
Humans
Neoplasm Invasiveness
Plasmids - genetics
Recombinant Proteins - biosynthesis
Recombinant Proteins - genetics
Transfection
Urinary Bladder Neoplasms - genetics
Urinary Bladder Neoplasms - pathology
基因多肽
基因转化
肿瘤入侵
膀胱肿瘤
title Effects of Gene Tranfection with CH50 Polypeptide on the Invasion Ability of Bladder Cancer Cell Line BIU-87
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