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氯化镉诱发人支气管上皮细胞恶性转化中hMSH2基因mRNA表达变化 被引量:3

Expression of hMSH2 mRNA during malignant transforming stages of 16HBE cells induced by cadmium chloride
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摘要 目的探讨氯化镉诱发人支气管上皮细胞系(16HBE)恶性转化过程中hMSH2基因mRNA动态变化的规律。方法用反转录-聚合酶链反应(PT-PCR)技术检测16HBE、氯化镉恶性转化16HBE系不同阶段(第5、15、32代细胞及成瘤细胞)hMSH2基因mRNA的表达情况。结果随着转化代数的增加,hMSH2基因mRNA的表达逐渐降低,到第32代细胞后表达明显下降(P<0.01)。结论氯化镉诱发16HBE系恶性转化过程中hMSH2基因表达逐渐下降,hMSH2基因水平的改变可能是氯化镉的致癌机制之一。 Objective To explore the expression of hMSH2 mRNA during the malignant transforming stages of 16HBE cells induced by cadmium chloride. Methods Reverse transcription-polymerase chain reaction (RT-PCR) was used to measure the expression ofhMSH2 mRNA in 16HBE cells and its different passage cells treated by cadmium chloride (the 5th , 15th, 32th passage, and neoplasmed cells from nude mice' s tumor tissue). Results With the passages of 16HBE cells treated with cadmium chloride increased, the expression of hMSH2 gene decreased gradually ( P 〈 0.01 ). Conclusion During transformation from 16HBE cells to malignant transformation induced by cadmium chloride, the expression of hMSH2 gene decreased, the alteration of hMSH2 gene may be a possible carcinogenic mechanism for cadmium chloride.
出处 《中国职业医学》 CAS 北大核心 2007年第5期375-377,共3页 China Occupational Medicine
基金 国家自然科学基金资助项目(30771781) 广东省自然科学基金资助项目(06022672) 广州市科技攻关重点资助项目(2003Z2-E0191/E0192) 广州市属高校科技计划项目(1002)
关键词 氯化镉 人支气管上皮细胞(16HBE) HMSH2基因 Cadmium chloride (CdCh) Human bronchial epithelial (16HBE) cells hMSH2 gene
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  • 1HARTWIG A. Role of DNA repair inhibition in lead-and cadmiuminduced genotoxicity: a review[ J]. Environ Health Perspect, 1994, 102( Suppl 3 ) :45 -50.
  • 2FATUR T, LAH T T, FILIPIC M. Cadmium inhibits repair of UV-, methyl methanesulfonate-and N-muthyl-N-nitrosourea-induced DNA damage in Chinese hamster ovary cells[J]. Murat Ras,2003,529( 1/2) ;109 - 116.
  • 3YU Z, CHEN J, FORD B N, et al. Human DNA repair systems: an overview[ J]. Environ Mol Mutagen, 1999, 33( 1 ) :3 -20.
  • 4KOLODNER R D, HALL N R, LIPFORD J,et al. Structure of the human MSH2 locus and analysis of two Muir-Torte kindreds for msh2 mutations[J]. Genomics, 1994, 24(3) :516 -526.
  • 5CALSOU P, FRIT P, BOZZATO C, et al. Negative interference of metal (II) ions with nucleotide excision repair in human cell-free extracts[ J]. Carcinogenesis, 1996, 17 (12) :2779 - 2782.
  • 6HARTWIG A. Carcinogenlcity of metal compounds: possible role of DNA repair inhibition[J]. Toxicol Left, 1998, 102 -103:235 -239.
  • 7YONG H J, ALAN B C , ROBBERT J C, et al. Cadmium is a mutagen that acts by inhibiting mismatch repair. Nature genetics, 2003, 34(3) : 326 -329.
  • 8JOSEPH P, MUCHNOK T, ONG T. Gene expression profile in BALB/c-3T3 cells transformed with beryllium sulfate [ J ]. Mol Carcinog, 2001,32( 1 ) :28 -35.
  • 9SNOW E T. Metal carcinogenesis: mechanistic implications [ J ]. Pharmacol Ther, 1992,53 ( 1 ) :31 - 65.
  • 10PELTOMAKI P. DNA mismatch repair gene mutations in human cancer[J]. Environ Health Perspect, 1997, 105(Suppl 4) : 775 - 780.

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