The Xiphophorus hybrid melanoma model represents one of the earliest reported cases of genetically regulated tumor susceptibility. Melanoma formation in Xiphophorus hybrids may be explained by the inheritance of two genes: a sex-inked oncogene, Xmrk, and a putative tumor suppressor locus, termed DIFF, located in Linkage Group V (LGV). Several genetic mapping procedures were used to produce a new Xiphophorus LGV map with 20 loci. All markers, particularly a recently cloned Xiphophorus CDKN2 gene family member, called CDKN2X, were tested for associations of genotype with degree of macromelanophore pigment pattern modification and susceptibility to melanoma formation in backcross hybrids of seven genetic types, involving 1,110 fish and three pigment patterns. Highly significant associations of CDKN2X genotypes with such phenotypic effects suggests that this gene is a strong candidate for the classically defined DIFF tumor suppressor gene. Because published results have documented the involvement of the CDKN2A (p16, MTSI, and INK4A) tumor suppressor gene in human melanoma formation, the possibility of CDKN2 genes acting as tumor suppressors in both man and Xiphophorus is likely.
|Original language||English (US)|
|Number of pages||11|
|Journal||Genes Chromosomes and Cancer|
|State||Published - Jul 1998|
ASJC Scopus subject areas
- Cancer Research