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脆性组氨酸三联体基因异常转录与肝癌关系的研究 被引量:4

Relationship between aberrant FHIT transcripts and hepatocellular carcinoma
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摘要 目的 研究脆性组氨酸二联体(FHIT)基因异常转录与肝细胞癌(HCC)的相关性。方法利用逆转录-聚合酶链反应(RT-PCR)和单链构象多态性(SSCP)技术检测24对肝癌及癌旁组织、4例正常肝组织中FHIT的转录和突变情况。结果 11例肝癌组织(46%)标本、2例(8%)癌旁正常组织检测到异常转录本,正常肝组织无异常转录。结论 FHIT基因异常转录可能是导致肝细胞癌形成的一个重要因素。 Objective To study the relationship between aberrant FHIT transcripts and hepatocellular carcinoma (HCC), Methods Reverse transcription-polymerase chain reaction (RT-PCR) and single strand conforma-tional polymorphism (SSCP) assays were used to analyze the transcripts and mutations of FHIT gene in 24 matched tumorous tissues and para-tumorous tissues from patients with HCC and in 4 normal liver tissues. Results Aberrant FHIT transcripts were observed in 11 out of 24 (46%) tumorous tissues and in 2 (8%) of the matched para-tumorous tissues. Conclusion FHIT aberrant transcripts may play an important role in the pathogenesis of hepatocellular carcinoma.
出处 《中华肝脏病杂志》 CAS CSCD 2003年第9期550-551,共2页 Chinese Journal of Hepatology
基金 铁道部医学专项基金(TW200027)
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  • 1王兴元,孙燕,李卫东,王秀琴,张和平,程金科,丁芳,吴.肺癌组织和转移性肺门淋巴结中FHIT基因和p16基因的变化[J].中华肿瘤杂志,1999,21(2):108-111. 被引量:25
  • 2Ohta M, Inoue H, Cotticelli MG, et al. The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3; 8) breakpoint, is abnormal in digestive tract cancer. Cell, 1996,84: 587-597.
  • 3Barnes LD, Garrison PN, Siprashvili Z, et al. Fhit, a putative tumor suppressor in humans, is a dinucleoside 5', 5'"-pl, p3-triphosphate hydrolase. Biochemistry, 1996, 35:11529-11535.
  • 4Sozzi G, Veronese ML, Negrini M, et al. The FHIT gene 3p14.2 is abnormal in lung cancer. Cell, 1996, 85: 17-26.
  • 5Mao L, Fan YH, Lotan R, et al. Frequent abnormalities of FHIT, a candidate tumor suppressor gene, in head and neck cancer cell lines.Cancer Res,1996, 56: 5128-5131.
  • 6Yuan BZ, Keck-Waggoner C, Zimonjic DB, et al. Alterations of the FHIT gene in human hepatocellular carcinoma. Cancer Res, 2000,60: 1049-1053.

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