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Frequency of homozygous deletion at p16/CDKN2 in primary human tumours.

Publication ,  Journal Article
Cairns, P; Polascik, TJ; Eby, Y; Tokino, K; Califano, J; Merlo, A; Mao, L; Herath, J; Jenkins, R; Westra, W; Rutter, JL; Buckler, A; Cho, KR ...
Published in: Nat Genet
October 1995

Many tumour types have been reported to have deletion of 9p21 (refs 1-6). A candidate target suppressor gene, p16 (p16INK4a/MTS-1/CDKN2), was recently identified within the commonly deleted region in tumour cell lines. An increasing and sometimes conflicting body of data has accumulated regarding the frequency of homozygous deletion and the importance of p16 in primary tumours. We tested 545 primary tumours by microsatellite analysis with existing and newly cloned markers around the p16 locus. We have now found that small homozygous deletions represent the predominant mechanism of inactivation at 9p21 in bladder tumours and are present in other tumour types, including breast and prostate cancer. Moreover, fine mapping of these deletions implicates a 170 kb minimal region that includes p16 and excludes p15.

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Published In

Nat Genet

DOI

ISSN

1061-4036

Publication Date

October 1995

Volume

11

Issue

2

Start / End Page

210 / 212

Location

United States

Related Subject Headings

  • Polymerase Chain Reaction
  • Neoplasms
  • Male
  • In Situ Hybridization, Fluorescence
  • Humans
  • Homozygote
  • Genetic Markers
  • Genes, Tumor Suppressor
  • Female
  • Developmental Biology
 

Citation

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MLA
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Cairns, P., Polascik, T. J., Eby, Y., Tokino, K., Califano, J., Merlo, A., … Sidransky, D. (1995). Frequency of homozygous deletion at p16/CDKN2 in primary human tumours. Nat Genet, 11(2), 210–212. https://doi.org/10.1038/ng1095-210
Cairns, P., T. J. Polascik, Y. Eby, K. Tokino, J. Califano, A. Merlo, L. Mao, et al. “Frequency of homozygous deletion at p16/CDKN2 in primary human tumours.Nat Genet 11, no. 2 (October 1995): 210–12. https://doi.org/10.1038/ng1095-210.
Cairns P, Polascik TJ, Eby Y, Tokino K, Califano J, Merlo A, et al. Frequency of homozygous deletion at p16/CDKN2 in primary human tumours. Nat Genet. 1995 Oct;11(2):210–2.
Cairns, P., et al. “Frequency of homozygous deletion at p16/CDKN2 in primary human tumours.Nat Genet, vol. 11, no. 2, Oct. 1995, pp. 210–12. Pubmed, doi:10.1038/ng1095-210.
Cairns P, Polascik TJ, Eby Y, Tokino K, Califano J, Merlo A, Mao L, Herath J, Jenkins R, Westra W, Rutter JL, Buckler A, Gabrielson E, Tockman M, Cho KR, Hedrick L, Bova GS, Isaacs W, Koch W, Schwab D, Sidransky D. Frequency of homozygous deletion at p16/CDKN2 in primary human tumours. Nat Genet. 1995 Oct;11(2):210–212.

Published In

Nat Genet

DOI

ISSN

1061-4036

Publication Date

October 1995

Volume

11

Issue

2

Start / End Page

210 / 212

Location

United States

Related Subject Headings

  • Polymerase Chain Reaction
  • Neoplasms
  • Male
  • In Situ Hybridization, Fluorescence
  • Humans
  • Homozygote
  • Genetic Markers
  • Genes, Tumor Suppressor
  • Female
  • Developmental Biology