Variable FHIT transcripts in non‐neoplastic tissues
- 1 August 1997
- journal article
- Published by Wiley in Genes, Chromosomes and Cancer
- Vol. 19 (4) , 215-219
- https://doi.org/10.1002/(sici)1098-2264(199708)19:4<215::aid-gcc2>3.0.co;2-#
Abstract
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.Keywords
This publication has 6 references indexed in Scilit:
- FHIT gene alterations in head and neck squamous cell carcinomas.Proceedings of the National Academy of Sciences, 1996
- Chromosome aberrations in prophylactic mastectomies from women belonging to breast cancer familiesGenes, Chromosomes and Cancer, 1996
- The FHIT Gene at 3p14.2 Is Abnormal in Lung CancerCell, 1996
- The FHIT Gene, Spanning the Chromosome 3p14.2 Fragile Site and Renal Carcinoma–Associated t(3;8) Breakpoint, Is Abnormal in Digestive Tract CancersCell, 1996
- Tissue-dependent expression of a novel splice variant of the human oestrogen receptorThe Journal of Steroid Biochemistry and Molecular Biology, 1995
- Genomic sequencing.Proceedings of the National Academy of Sciences, 1984