Sozzi G, Veronese M L, Negrini M, Baffa R, Cotticelli M G, Inoue H, Tornielli S, Pilotti S, De Gregorio L, Pastorino U, Pierotti M A, Ohta M, Huebner K, Croce C M
Kimmel Cancer Center, Jefferson Medical College, Philadelphia, Pennsylvania 19107, USA.
Cell. 1996 Apr 5;85(1):17-26. doi: 10.1016/s0092-8674(00)81078-8.
To determine the role of the FHIT gene, which encompasses the fragile site at 3p14.2, we analyzed 59 tumors of the small cell and non-small cell type by reverse transcription of FHIT mRNA, followed by PCR amplification and sequencing of products. Allelic losses affecting the gene were evaluated by microsatellite polymorphism analysis and genomic alterations by hybridization using cDNA and genomic probes. Small cell lung tumors (80%) and non-small cell lung cancers (40%) showed abnormalities in RNA transcripts of FHIT, and 76% of the tumors exhibited loss of FHIT alleles. Abnormal lung tumor transcripts lack two or more exons of the FHIT gene. Small cell lung cancer tumors and cell lines were analyzed by Southern blotting and showed rearranged BamHI fragments. These data suggest a critical role of the FHIT gene in lung carcinogenesis.
为了确定包含3p14.2脆性位点的FHIT基因的作用,我们通过逆转录FHIT mRNA,随后进行PCR扩增和产物测序,分析了59例小细胞型和非小细胞型肿瘤。通过微卫星多态性分析评估影响该基因的等位基因缺失,并使用cDNA和基因组探针通过杂交评估基因组改变。小细胞肺癌肿瘤(80%)和非小细胞肺癌(40%)显示出FHIT RNA转录本异常,76%的肿瘤表现出FHIT等位基因缺失。异常的肺肿瘤转录本缺少FHIT基因的两个或更多外显子。通过Southern印迹分析小细胞肺癌肿瘤和细胞系,显示BamHI片段重排。这些数据表明FHIT基因在肺癌发生中起关键作用。