The tumor-suppressor gene FHIT is involved in the regulation of apoptosis and in cell cycle control

Laura Sard, Paola Accornero, Silvana Tornielli, Domenico Delia, Giuseppe Bunone, Manuela Campiglio, Mario P. Colombo, Marcella Gramegna, Carlo M. Croce, Marco A. Pierotti, Gabriella Sozzi

Research output: Contribution to journalArticlepeer-review


Alteration of the FHIT (fragile histidine triad) gene occurs as an early and frequent event in lung carcinogenesis. FHIT gene transfer into lung cancer cell line H460 lacking Fhit protein expression resulted in reversion of tumorigenicity. To gain insight into the biological function of FHIT, we compared the H460 cell line with its Fhit transfectants (H460/FHIT). A significant inhibition of cell growth was observed in H460/FHIT cells. The analysis of apoptosis by in situ terminal deoxynucleotidyltransferase- mediated dUTP nick end labeling revealed a high rate of apoptosis-induced DNA strand breaks in stable clones. In situ results were confirmed by FACScan analysis that showed an apoptotic rate of 44-47% compared with a 15% level in the control H460 cells. Analysis of cell cycle-phase distribution indicated a significant G0/G1 arrest and the presence of a sub-G1 peak in the stable clones. No significant changes in Bcl2, BclX, and Bax protein expression level were observed in the transfected clones as compared with the control H460 cells whereas a 2-fold increase in Bak protein levels was noticed. An increased level of p21(waf) protein paralleled by an up-regulation of p21(waf) transcripts also was found in Fhit-expressing clones compared with the H460 cell line. No differences in p53 levels were observed in the same cells, suggesting a p53-independent effect. These data suggest that the observed growth-inhibitory effect in FHIT-reexpressing cells could be related to apoptosis and cell cycle arrest and link the tumor-suppressor activity of FHIT to its proapoptotic function.

Original languageEnglish
Pages (from-to)8489-8492
Number of pages4
JournalProceedings of the National Academy of Sciences of the United States of America
Issue number15
Publication statusPublished - Jul 20 1999

ASJC Scopus subject areas

  • Genetics
  • General


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