Panagopoulos I, Thelin S, Mertens F, Mitelman F, Aman P
Department of Clinical Genetics, University Hospital, Lund, Sweden.
Genes Chromosomes Cancer. 1997 Aug;19(4):215-9. doi: 10.1002/(sici)1098-2264(199708)19:4<215::aid-gcc2>3.0.co;2-#.
We used nested reverse transcriptase PCR to investigate the expression of the FHIT gene, a presumptive tumor suppressor gene located in chromosomal band 3p 14.2, in non-neoplastic samples. Multiple transcripts of the FHIT gene were found in peripheral blood lymphocytes, skeletal muscle, and liver of healthy individuals, as well as in a cell line derived from isynovial tissue. The data indicate that variable splicing of the FHIT transcript, leading to deletions of exons and thus anomalous or absent FHIT protein production, occurs frequently in non-neoplastic tissues. Hence, the finding of multiple nonfunctional FHIT transcripts is not tumor-specific and cannot be used as a genetic marker of neoplasia.
我们采用巢式逆转录聚合酶链反应(nested reverse transcriptase PCR)来研究FHIT基因(一种位于染色体3p 14.2带的推定肿瘤抑制基因)在非肿瘤性样本中的表达。在健康个体的外周血淋巴细胞、骨骼肌和肝脏以及来自滑膜组织的细胞系中发现了FHIT基因的多种转录本。数据表明,FHIT转录本的可变剪接导致外显子缺失,从而产生异常或缺乏FHIT蛋白,这种情况在非肿瘤性组织中经常发生。因此,发现多种无功能的FHIT转录本并非肿瘤特异性,不能用作肿瘤形成的遗传标志物。