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膀胱癌相关蛋白基因的功能分析:一种推测的宫颈癌抑癌基因

Functional analysis of bladder cancer-related protein gene: a putative cervical cancer tumor suppressor gene in cervical carcinoma.

作者信息

Zuo Zehua, Zhao Min, Liu Juan, Gao Guifang, Wu Xinxing

机构信息

Wuhan University, Wuhan, China.

出版信息

Tumour Biol. 2006;27(4):221-6. doi: 10.1159/000093057. Epub 2006 May 2.

DOI:10.1159/000093057
PMID:16675915
Abstract

Our previous study has suggested thatthe bladder cancer-associated protein gene (BLCAP) was among the differentially expressed genes in cervical cancer. We confirm here that BLCAP is expressed in all noncancerous cervical tissues (10/10), but it is greatly lost in primary cervical cancer tissue (31/39). In order to further investigate the functional roles of BLCAP, we stably transfected BLCAP cDNA into HeLa cells. The HeLa cells expressing BLCAP show reduced cell growth and clone genicity compared to the vector-transfected cognate cells. BLCAP expression in HeLa cells leads to growth arrest and significantly enhanced apoptosis in vitro and reduced tumor formation in vivo. Thus, BLCAP might be a potential tumor suppressor gene in cervical carcinoma.

摘要

我们之前的研究表明,膀胱癌相关蛋白基因(BLCAP)是宫颈癌中差异表达的基因之一。我们在此证实,BLCAP在所有非癌性宫颈组织中均有表达(10/10),但在原发性宫颈癌组织中其表达大量缺失(31/39)。为了进一步研究BLCAP的功能作用,我们将BLCAP cDNA稳定转染至HeLa细胞。与载体转染的同源细胞相比,表达BLCAP的HeLa细胞显示出细胞生长和克隆形成能力降低。HeLa细胞中BLCAP的表达导致体外生长停滞、凋亡显著增强以及体内肿瘤形成减少。因此,BLCAP可能是宫颈癌中的一个潜在抑癌基因。

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1
Functional analysis of bladder cancer-related protein gene: a putative cervical cancer tumor suppressor gene in cervical carcinoma.膀胱癌相关蛋白基因的功能分析:一种推测的宫颈癌抑癌基因
Tumour Biol. 2006;27(4):221-6. doi: 10.1159/000093057. Epub 2006 May 2.
2
[Inhibitory effect of bladder cancer related protein gene on HeLa cell proliferation].膀胱癌相关蛋白基因对HeLa细胞增殖的抑制作用
Ai Zheng. 2006 Jul;25(7):811-7.
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BLCAP arrests G₁/S checkpoint and induces apoptosis through downregulation of pRb1 in HeLa cells.BLCAP在HeLa细胞中通过下调pRb1来阻止G₁/S期检查点并诱导细胞凋亡。
Oncol Rep. 2016 May;35(5):3050-8. doi: 10.3892/or.2016.4686. Epub 2016 Mar 17.
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A-to-I RNA editing of BLCAP lost the inhibition to STAT3 activation in cervical cancer.宫颈癌中BLCAP的A到I RNA编辑丧失了对STAT3激活的抑制作用。
Oncotarget. 2017 Jun 13;8(24):39417-39429. doi: 10.18632/oncotarget.17034.
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Differential gene expression in cervical cancer cell lines before and after ionizing radiation.电离辐射前后宫颈癌细胞系中的差异基因表达
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Expression of homeobox genes in cervical cancer.同源框基因在宫颈癌中的表达。
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Suppression of tumorigenesis by transcription units expressing the antisense E6 and E7 messenger RNA (mRNA) for the transforming proteins of the human papilloma virus and the sense mRNA for the retinoblastoma gene in cervical carcinoma cells.在宫颈癌细胞中,通过表达针对人乳头瘤病毒转化蛋白的反义E6和E7信使核糖核酸(mRNA)以及视网膜母细胞瘤基因的正义mRNA的转录单位来抑制肿瘤发生。
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Aristolochic acid I interferes with the expression of BLCAP tumor suppressor gene in human cells.马兜铃酸 I 干扰人细胞中 BLCAP 肿瘤抑制基因的表达。
Toxicol Lett. 2018 Jul;291:129-137. doi: 10.1016/j.toxlet.2018.03.032. Epub 2018 Apr 12.
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Bladder cancer-associated protein is suppressed in human cervical tumors.膀胱癌相关蛋白在人类宫颈肿瘤中受到抑制。
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Cancer Res. 2003 Apr 15;63(8):1888-93.

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Identification of BLCAP as a novel STAT3 interaction partner in bladder cancer.鉴定BLCAP作为膀胱癌中一种新的STAT3相互作用蛋白。
PLoS One. 2017 Nov 30;12(11):e0188827. doi: 10.1371/journal.pone.0188827. eCollection 2017.
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A-to-I RNA editing of BLCAP lost the inhibition to STAT3 activation in cervical cancer.宫颈癌中BLCAP的A到I RNA编辑丧失了对STAT3激活的抑制作用。
Oncotarget. 2017 Jun 13;8(24):39417-39429. doi: 10.18632/oncotarget.17034.
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Immunoexpression analysis and prognostic value of BLCAP in breast cancer.乳腺癌中 BLCAP 的免疫表达分析及其预后价值。
PLoS One. 2012;7(9):e45967. doi: 10.1371/journal.pone.0045967. Epub 2012 Sep 25.
6
Bladder cancer-associated protein is suppressed in human cervical tumors.膀胱癌相关蛋白在人类宫颈肿瘤中受到抑制。
Exp Ther Med. 2012 Feb;3(2):336-340. doi: 10.3892/etm.2011.408. Epub 2011 Dec 5.
7
Human BLCAP transcript: new editing events in normal and cancerous tissues.人 BLCAP 转录本:正常和癌组织中的新剪接事件。
Int J Cancer. 2010 Jul 1;127(1):127-37. doi: 10.1002/ijc.25022.
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Bladder cancer-associated protein, a potential prognostic biomarker in human bladder cancer.膀胱癌相关蛋白,人类膀胱癌潜在的预后生物标志物。
Mol Cell Proteomics. 2010 Jan;9(1):161-77. doi: 10.1074/mcp.M900294-MCP200. Epub 2009 Sep 25.
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