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Publication : Fhit modulates the DNA damage checkpoint response.

First Author  Ishii H Year  2006
Journal  Cancer Res Volume  66
Issue  23 Pages  11287-92
PubMed ID  17145874 Mgi Jnum  J:116214
Mgi Id  MGI:3693176 Doi  10.1158/0008-5472.CAN-06-2503
Citation  Ishii H, et al. (2006) Fhit modulates the DNA damage checkpoint response. Cancer Res 66(23):11287-92
abstractText  In preneoplastic lesions, the DNA damage checkpoint is induced and loss of heterozygosity at the FRA3B/FHIT common chromosome fragile region precedes or is coincident with activation of the checkpoint response in these early stages. Introduction of exogenous Fhit into cells in vitro led to modulation of expression of checkpoint proteins Hus1 and Chk1 at mid-S checkpoint, a modulation that led to induction of apoptosis in esophageal cancer cells but not in noncancerous primary cultures. Mutation of the conserved Fhit tyrosine 114 resulted in failure of this function, confirming the importance of this residue. The results suggest that the DNA damage-susceptible FRA3B/FHIT chromosome fragile region, paradoxically, encodes a protein that is necessary for protecting cells from accumulation of DNA damage through its role in modulation of checkpoint proteins, and inactivation of Fhit contributes to accumulation of abnormal checkpoint phenotypes in cancer development.
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