Cancer and the FRA3B/FHIT fragile locus: it's a HIT
Kay Huebner, Carlo Maria Croce
Abstract
Open-access reader
Kay Huebner, Carlo Maria Croce
Abstract
Open-access reader
The FHIT gene encompassing the most active common human chromosomal fragile region, FRA3B, was discovered in 1996 and proposed as a tumour suppressor gene for important human cancers. Seven years and more than 350 reports later, early questions concerning its tumour suppressor role have been answered. Recent studies on the role of Fhit loss in major types of human cancers report association with high proliferative and low apoptotic indices, node positivity, loss of mismatch repair protein, likelihood of progression and reduced survival.
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The FHIT gene encompassing the most active common human chromosomal fragile region, FRA3B, was discovered in 1996 and proposed as a tumour suppressor gene for important human cancers. Seven years and more than 350 reports later, early questions concerning its tumour suppressor role have been answered. Recent studies on the role of Fhit loss in major types of human cancers report association with high proliferative and low apoptotic indices, node positivity, loss of mismatch repair protein, likelihood of progression and reduced survival.
Key concepts: FHIT, Chromosomal fragile site, Locus (genetics), Tumor suppressor gene, Suppressor, WWOX, Cancer research, Biology