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Gene Review

Loh2  -  loss of heterozygosity, region 2

Mus musculus

 
 
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Disease relevance of Loh2

  • This chromosomal region is deleted in early stages of tumorigenesis of mouse islet cell carcinomas and contains the hitherto unidentified Loh2 gene, a putative suppressor of angiogenesis [1].
 

High impact information on Loh2

  • The locus on chromosome 9, named Loh-1, lies in a region with synteny conservation to human chromosomes 3q, 6q12, 15q24, and 3p21, while the locus on chromosome 16, named Loh-2, lies in a region corresponding to human chromosomes 3q and 22q [2].
  • The observation that a high LOH rate at Loh2 is seen in the angiogenic islet stage suggests that this locus may contain an angiogenesis suppressor; in contrast, the later appearance of Loh1 may contribute to the progression from the angiogenic stage to a solid tumor [3].
 

Biological context of Loh2

References

  1. Cloning and chromosomal mapping of the human p53-related KET gene to chromosome 3q27 and its murine homolog Ket to mouse chromosome 16. Augustin, M., Bamberger, C., Paul, D., Schmale, H. Mamm. Genome (1998) [Pubmed]
  2. Genome-wide search for loss of heterozygosity in transgenic mouse tumors reveals candidate tumor suppressor genes on chromosomes 9 and 16. Dietrich, W.F., Radany, E.H., Smith, J.S., Bishop, J.M., Hanahan, D., Lander, E.S. Proc. Natl. Acad. Sci. U.S.A. (1994) [Pubmed]
  3. Tumor suppressor loci on mouse chromosomes 9 and 16 are lost at distinct stages of tumorigenesis in a transgenic model of islet cell carcinoma. Parangi, S., Dietrich, W., Christofori, G., Lander, E.S., Hanahan, D. Cancer Res. (1995) [Pubmed]
 
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