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长期砷诱导L-02细胞的表达谱基因芯片实验 被引量:3

Expression fingerprint analysis of chronic arsenite-induced L-02 cell using cDNA microarry
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摘要 目的 :采用基因芯片技术研究长期砷染毒时人正常肝细胞 (L 0 2细胞 )基因表达谱的变化 .方法 :4 μmol/LNaAsO2染毒人正常肝细胞 (L 0 2细胞 ) 2wk以上与未染毒的L 0 2细胞做表达谱基因芯片杂交 .结果 :长期砷染毒后细胞基因出现多方面表达差异 ,既包括细胞一些正常生理功能如生长发育、分裂增殖相关的基因 ,同时也包含一些与肿瘤发生、发展有关的基因 .结论 :细胞长期暴露于砷环境后多种与肿瘤发生有关的基因差异表达 。 AIM: To investigate the expression profile of human genes in response to chronic sodium arsenite treatment by cDNA microarrays. METHODS: The RNA was purified from the L 02 cells without and with 4 μmol/L arsenite sodium induction for more than 2 weeks, respectively. RESULTS: In long term exposure, many genes were aberrantly expressed, which included genes involved in cell cycle regulation, signal transduction, stress response and growth factor and various oncogenes. CONCLUSION: Many tumor related genes are aberrantly expressed when cells are exposed to arsenic environment for more than two weeks, which may offer some clues to further studies on carcinogenesis and arsenite.
出处 《第四军医大学学报》 北大核心 2004年第13期1205-1207,共3页 Journal of the Fourth Military Medical University
基金 国家自然科学基金 (30 0 60 0 74) 兵团专项基金(NKB0 1SDXNK41YX)
关键词 eDNA基因芯片 L-02细胞 arsenite cDNA microarry L 02 cell
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参考文献11

  • 1Goering PL, Aposhian HV, Mass MJ, et al. The enigma of arsenic carcinogenesis: Role of metabolism[J]. Toxicol Sci, 1999; 49(1):5-14.
  • 2Abernathy CO, Liu YP, Longfellow D, et al. Arsenic: Health effects, mechanisms of actions, and research issues[J]. Environ Health Perspect, 1999;107(7):593-597.
  • 3Huff J, Chan P, Nyska A. Is the human carcinogen arsenic carcinogenic to laboratory animals[J]? Toxicol Sci, 2000;55(1):17-23.
  • 4Schena M, Shalon D, Dais RW, et al. Quantitative monitoring of gene expression patterns with a complementary DNA microarray[J]. Science, 1995; 270(20): 467-470.
  • 5顾永清,杨磊,袁红玲,吴超群,潘泽民,夏放,李瑶,应康,谢毅.砷代谢相关的全长新cDNA的克隆和功能初步研究[J].复旦学报(自然科学版),2000,39(6):603-608. 被引量:11
  • 6Ratajczak MZ, Kant JA, Luger SM, et al. In vivo treatment of human leukemia in a scid mouse model with c-myb antisense oligodeoxynucleotides[J]. Proc Natl Acad Sci USA, 1992;89(24):11823-11827.
  • 7Tommerup N, Vissing H. Isolation and fine mapping of 16 novel human zinc finger-encoding cDNAs identify putative candidate genes for developmental and malignant disorders [J]. Genomics, 1995; 27(2):259-264.
  • 8Meuwissen RL, Meerts I, Hoovers JM, et al. Human synaptonemal complex protein 1 (SCP1): Isolation and characterization of the cDNA and chromosomal localization of the gene[J]. Genomics, 1997; 39(3): 377-384.
  • 9Fornerod M, Ohno M, Yoshida M, et al. CRM1 is an export receptor for leucine-rich nuclear export signals [J]. Cell, 1997; 90(6):1051-1060.
  • 10Kudo N, Khochbin S, Nishi K, et al. Molecular cloning and cell cycle-dependent expression of mammalian CRM1, a protein involved in nuclear export of proteins [J]. J Biol Chem, 1997;272(47):29742-29751.

二级参考文献11

  • 1奥斯伯F 布伦斯RE 等.精编分子生物学指南[M].北京:科学出版社,1998..
  • 2汪玮,复旦学报,2000年,39卷,6期,588页
  • 3周宗祥,复旦学报,2000年,39卷,6期,583页
  • 4Yang Lei,Life and Clinical Medicine[C],2000年
  • 5Rossman T G,Carcinogenesis,1999年,2 0卷,2期,311页
  • 6Wang G Q,Chin Med J,1999年,112卷,20页
  • 7Xu C,J Bio Chem,1998年,12 3卷,16页
  • 8颜子颖(译),精编分子生物学实验指南,1998年
  • 9Wang Z,Toxicol Appl Pharmacl,1993年,118卷,80页
  • 10周宗祥,徐坚,等.RBM13 cDNA的克隆及其表达谱分析[J].复旦学报(自然科学版),2000,39(6):583-587. 被引量:19

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