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PMID: 7734302 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Colorectal carcinomas show frequent allelic loss on the long arm of chromosome 17 with evidence for a specific target region.

British journal of cancer ·Vol. 71 ·No. 5 ·1995-05-00 ·Pages 1070-3

Leggett B, Young J, Buttenshaw R, Thomas L, Young B, Chenevix-Trench G, Searle J, Ward M

Abstract

Allelic loss is a common mechanism of inactivation of tumour-suppressor genes in colorectal carcinomas. A number of known or putative tumour-suppressor genes including NF1, BRCA1, NME1, NME2 and prohibitin are present on the long arm of chromosome 17, and this region has not been extensively analysed in colorectal tumours. In this study 72 colorectal carcinomas were examined for allelic loss at eight loci on chromosome 17. Allelic loss was frequent both at the p53 locus, which is known to be important in colorectal carcinoma, and also telomeric to p53 on 17p. Allelic loss continued to be present in more than 50% of cases in the pericentromeric region and on proximal 17q to the marker LEW101 (D17S40) at 17q22-23. The most telomeric markers on 17q showed lower rates of allelic loss. Analysis of cases with partial deletions which did not include the p53 locus showed a common region of overlap of the deletions centred on D17S40. This suggests the target of allelic loss on 17q is a tumour-suppressor gene in this region.

Related Genes
MeSH Terms
Alleles Chromosomes, Human, Pair 17 Colorectal Neoplasms/genetics,pathology Evaluation Studies as Topic Gene Deletion Genes, Overlapping Genes, p53 Humans Neoplasm Staging
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Leggett B
Glaxo Gastroenterology Research Laboratory, Royal Brisbane Hospital Clinical Research Centre, Bancroft Centre, Australia.
Young J
Buttenshaw R
Thomas L
Young B
Chenevix-Trench G
Searle J
Ward M
References (37)
37 references, click to expand
  1. Genetic alterations during colorectal-tumor development.
    N Engl J Med. 1988 Sep 1;319(9):525-32 PMID: 2841597
  2. Isolation and mapping of a polymorphic DNA sequence (pYNZ22) on chromosome 17p [D17S30].
    Nucleic Acids Res. 1988 Jun 24;16(12):5707 PMID: 2455284
  3. Allelotype of colorectal carcinomas.
    Science. 1989 Apr 14;244(4901):207-11 PMID: 2565047
  4. Identification of a chromosome 18q gene that is altered in colorectal cancers.
    Science. 1990 Jan 5;247(4938):49-56 PMID: 2294591
  5. Cytogenetics of colorectal adenocarcinomas.
    Cancer Genet Cytogenet. 1990 Jun;46(2):143-56 PMID: 2340486
  6. A genetic model for colorectal tumorigenesis.
    Cell. 1990 Jun 1;61(5):759-67 PMID: 2188735
  7. Evidence implicating at least two genes on chromosome 17p in breast carcinogenesis.
    Lancet. 1990 Sep 29;336(8718):761-3 PMID: 1976143
  8. Loss of heterozygosity on chromosomes 17 and 18 in breast carcinoma: two additional regions identified.
    Proc Natl Acad Sci U S A. 1990 Oct;87(19):7737-41 PMID: 1977164
  9. p53 gene mutations occur in combination with 17p allelic deletions as late events in colorectal tumorigenesis.
    Cancer Res. 1990 Dec 1;50(23):7717-22 PMID: 2253215
  10. Somatic allelic deletion of nm23 in human cancer.
    Cancer Res. 1991 May 1;51(9):2490-3 PMID: 2015608
  11. A highly polymorphic cDNA probe in the NF1 gene.
    Nucleic Acids Res. 1991 Jul 11;19(13):3754 PMID: 1677185
  12. Association of nm23-H1 allelic deletions with distant metastases in colorectal carcinoma.
    Lancet. 1991 Sep 21;338(8769):722-4 PMID: 1679868
  13. Tumor suppressor genes.
    Science. 1991 Nov 22;254(5035):1138-46 PMID: 1659741
  14. Chromosomal localization and nucleoside diphosphate kinase activity of human metastasis-suppressor genes NM23-1 and NM23-2.
    Oncogene. 1993 Feb;8(2):497-502 PMID: 8381224
  15. Mutation in the nm23 gene is associated with metastasis in colorectal cancer.
    Cancer Res. 1993 Feb 15;53(4):717-20 PMID: 7916650
  16. Allele loss patterns on chromosome 17q in 109 breast carcinomas indicate at least two distinct target regions.
    Oncogene. 1993 Mar;8(3):781-5 PMID: 8437862
  17. A deletion unit on chromosome 17q in epithelial ovarian tumors distal to the familial breast/ovarian cancer locus.
    Cancer Res. 1993 Mar 15;53(6):1218-21 PMID: 8095178
  18. Four separate regions on chromosome 17 show loss of heterozygosity in familial breast carcinomas.
    Hum Genet. 1993 Mar;91(1):6-12 PMID: 8454289
  19. THRA1 and D17S183 flank an interval of < 4 cM for the breast-ovarian cancer gene (BRCA1) on chromosome 17q21.
    Am J Hum Genet. 1993 Apr;52(4):718-22 PMID: 8460637
  20. The human NME2 gene lies within 18kb of NME1 in chromosome 17.
    Genes Chromosomes Cancer. 1993 Apr;6(4):245-8 PMID: 7685630
  21. Detailed deletion mapping of chromosome 17q in ovarian and breast cancers: 2-cM region on 17q21.3 often and commonly deleted in tumors.
    Cancer Res. 1993 Jul 15;53(14):3382-5 PMID: 8100738
  22. A common region of deletion on chromosome 17q in both sporadic and familial epithelial ovarian tumors distal to BRCA1.
    Am J Hum Genet. 1994 Oct;55(4):666-77 PMID: 7942844
  23. BglII and EcoRI polymorphism of the human nm23-H1 gene (NME1).
    Nucleic Acids Res. 1991 Dec 11;19(23):6663 PMID: 1684428
  24. Loss of heterozygosity at the human RAP1A/Krev-1 locus is a rare event in colorectal tumors.
    Cancer Res. 1992 Jan 15;52(2):285-9 PMID: 1345809
  25. The human prohibitin gene located on chromosome 17q21 is mutated in sporadic breast cancer.
    Cancer Res. 1992 Mar 15;52(6):1643-6 PMID: 1540973
  26. Detection of frequent allelic loss on proximal chromosome 17q in sporadic breast carcinoma using microsatellite length polymorphisms.
    Cancer Res. 1992 May 1;52(9):2624-7 PMID: 1568230
  27. Somatic mutations in the neurofibromatosis 1 gene in human tumors.
    Cell. 1992 Apr 17;69(2):275-81 PMID: 1568247
  28. The NM23 gene maps to human chromosome band 17q22 and shows a restriction fragment length polymorphism with BglII.
    Genes Chromosomes Cancer. 1992 Jan;4(1):84-8 PMID: 1377015
  29. Early loss of heterozygosity on 17q in ovarian cancer. The Abe Ovarian Cancer Genetics Group.
    Oncogene. 1992 Oct;7(10):2069-72 PMID: 1408149
  30. Detection of loss of heterozygosity at the human TP53 locus using a dinucleotide repeat polymorphism.
    Genes Chromosomes Cancer. 1992 Jul;5(1):89-90 PMID: 1384667
  31. The prognostic value of substaging colorectal carcinoma. A prospective study of 1117 cases with standardized pathology.
    Cancer. 1987 Aug 15;60(4):852-7 PMID: 3594403
  32. Chromosome 5 allele loss in human colorectal carcinomas.
    Nature. 1987 Aug 13-19;328(6131):616-9 PMID: 2886919
  33. An anonymous single-copy clone, pC63, from chromosome 17q23-qter identifies a frequent RFLP [HGM9 No. D17S21].
    Nucleic Acids Res. 1987 Nov 11;15(21):9096 PMID: 2891104
  34. A hypervariable RFLP on chromosome 17p13 is defined by an arbitrary single copy probe p144-D6 [HGM9 No. D17S34].
    Nucleic Acids Res. 1987 Dec 23;15(24):10605 PMID: 2892175
  35. A simple salting out procedure for extracting DNA from human nucleated cells.
    Nucleic Acids Res. 1988 Feb 11;16(3):1215 PMID: 3344216
  36. Isolation and mapping of a polymorphic DNA sequence (pTHH59) on chromosome 17q [D17S4].
    Nucleic Acids Res. 1988 Apr 25;16(8):3598 PMID: 2897667
  37. A mapped set of DNA markers for human chromosome 17.
    Genomics. 1988 May;2(4):302-9 PMID: 2851536
Article Info
Journal
British journal of cancer
Abbr.
Br J Cancer
ISSN
0007-0920
Published
1995-05-00
Pages
1070-3
Language
English
Region
England
NLM ID
0370635
PMCID
PMC2033787
Subset
IM
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