The MTAP-CDKN2A Locus Confers Susceptibility to a Naturally Occurring Canine Cancer Running title: The MTAP-CDKN2A locus and a canine model for human cancers Key Words: Genome Wide Association Study, Dogs, p16, Cancer, Histiocytic sarcoma

نویسندگان

  • Abigail L. Shearin
  • Benoit Hedan
  • Edouard Cadieu
  • Suzanne A. Erich
  • Emmett V. Schmidt
  • Daniel L. Faden
  • John Cullen
  • Jerome Abadie
  • Erika M. Kwon
  • Andrea Gröne
  • Patrick Devauchelle
  • Maud Rimbault
  • Danielle M. Karyadi
  • Mary Lynch
  • Francis Galibert
  • Matthew Breen
  • Gerard R. Rutteman
  • Catherine André
  • Heidi G. Parker
  • Elaine A. Ostrander
چکیده

1 The MTAP-CDKN2A Locus Confers Susceptibility to a Naturally Occurring Canine Cancer Running title: The MTAP-CDKN2A locus and a canine model for human cancers

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The MTAP-CDKN2A locus confers susceptibility to a naturally occurring canine cancer.

BACKGROUND Advantages offered by canine population substructure, combined with clinical presentations similar to human disorders, makes the dog an attractive system for studies of cancer genetics. Cancers that have been difficult to study in human families or populations are of particular interest. Histiocytic sarcoma is a rare and poorly understood neoplasm in humans that occurs in 15% to 25% ...

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Homozygous deletion of CDKN2A and codeletion of the methylthioadenosine phosphorylase gene in the majority of pleural mesotheliomas.

PURPOSE Homozygous deletions at chromosome region 9p21 targeting the CDKN2A gene have been reported as a common cytogenetic abnormality in mesothelioma. MTAP, a gene approximately 100-kb telomeric to CDKN2A, encodes methylthioadenosine phosphorylase, an enzyme essential in the salvage of cellular adenine and methionine, and its codeletion with CDKN2A has been reported in other tumors. The aim o...

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Homozygous deletions of methylthioadenosine phosphorylase in human biliary tract cancers.

The p16(INK4A)/CDKN2A gene on chromosome 9p21 is a site of frequent allelic loss in human cancers, and in a subset of cases, homozygous deletions at this locus encompass the telomeric methylthioadenosine phosphorylase (MTAP) gene. The MTAP gene product is the principal enzyme involved in purine synthesis via the salvage pathway, such that MTAP-negative cancers are solely dependent on de novo pu...

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Fine-mapping loss of gene architecture at the CDKN2B (p15INK4b), CDKN2A (p14ARF, p16INK4a), and MTAP genes in head and neck squamous cell carcinoma.

OBJECTIVE To identify the extent and the smallest region of loss for CDKN2B(INK4b), CDKN2A(ARF,INK4a), and MTAP. Homozygous deletions of human chromosome 9p21 occur frequently in malignant cell lines and are common in squamous cell carcinoma of the head and neck (HNSCC). This complex region encodes the tumor suppressor genes cyclin-dependent kinase 2B (CDKN2B) (p15(INK4b)) and CDKN2A (p14(ARF),...

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Mice heterozygous for germ-line mutations in methylthioadenosine phosphorylase (MTAP) die prematurely of T-cell lymphoma.

Large homozygous deletions of 9p21 that inactivate CDKN2A, ARF, and MTAP are common in a wide variety of human cancers. The role for CDKN2A and ARF in tumorigenesis is well established, but whether MTAP loss directly affects tumorigenesis is unclear. MTAP encodes the enzyme methylthioadenosine phosphorylase, a key enzyme in the methionine salvage pathway. To determine if loss of MTAP plays a fu...

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تاریخ انتشار 2012