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Scram1 is a modifier of spinal cord resistance for astrocytoma on mouse Chr 5

  1. Author:
    Amlin-Van Schaick, J.
    Kim, S.
    Broman, K. W.
    Reilly, K. M.
  2. Author Address

    [Amlin-Van Schaick, Jessica; Reilly, Karlyne M.] NCI, Mouse Canc Genet Program, Frederick, MD 21702 USA. [Amlin-Van Schaick, Jessica] George Washington Univ, Inst Biomed Sci, Washington, DC 20037 USA. [Kim, Sungjin; Broman, Karl W.] Univ Wisconsin, Sch Med & Publ Hlth, Dept Biostat & Med Informat, Madison, WI 53706 USA.;Reilly, KM (reprint author), NCI, Mouse Canc Genet Program, W 7th St,Ft Detrick,POB B, Frederick, MD 21702 USA;ReillyK@mail.nih.gov
    1. Year: 2012
    2. Date: Apr
  1. Journal: Mammalian Genome
    1. 23
    2. 3-4
    3. Pages: 277-285
  2. Type of Article: Article
  3. ISSN: 0938-8990
  1. Abstract:

    Tumor location can profoundly affect morbidity and patient prognosis, even for the same tumor type. Very little is known about whether tumor location is determined stochastically or whether genetic risk factors can affect where tumors arise within an organ system. We have taken advantage of the Nf1-/+;Trp53-/+cis mouse model of astrocytoma/glioblastoma to map genetic loci affecting whether astrocytomas are found in the spinal cord. We identify a locus on distal Chr 5, termed Scram1 for spinal cord resistance to astrocytoma modifier 1, with a LOD score of 5.0 and a genome-wide significance of P < 0.004. Mice heterozygous for C57BL/6Jx129S4/SvJae at this locus show less astrocytoma in the spinal cord compared to 129S4/SvJae homozygous mice, although we have shown previously that 129S4/SvJae mice are more resistant to astrocytoma than C57BL/6J. Furthermore, the astrocytomas that are found in the spinal cord of Scram1 heterozygous mice arise in older mice. Because spinal cord astrocytomas are very rare and difficult to treat, a better understanding of the genetic factors that govern astrocytoma in the spine may lead to new targets of therapy or prevention.

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External Sources

  1. DOI: 10.1007/s00335-011-9380-0
  2. WOS: 000301304600006

Library Notes

  1. Fiscal Year: FY2011-2012
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