Literature DB >> 3468057

Nineteen of 26 cellular oncogenes precisely localized in the human genome map to one of the 83 bands involved in primary cancer-specific rearrangements.

S Heim, F Mitelman.   

Abstract

A total of 83 bands have been found to be specifically involved in primary structural chromosome rearrangements in human cancer. We have compared the distribution of these cancer-specific breakpoints with the chromosomal sites of the 26 cellular oncogenes currently mapped to individual bands within the human genome. Nineteen of the 26 oncogenes are localized in cancer-associated bands. This clustering of oncogene sites and cancer breakpoints is statistically highly significant (P = 0.0000012).

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Year:  1987        PMID: 3468057     DOI: 10.1007/BF00273843

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  13 in total

Review 1.  Evolution of tumours and the impact of molecular oncology.

Authors:  G Klein; E Klein
Journal:  Nature       Date:  1985 May 16-22       Impact factor: 49.962

2.  Proliferation-specific and differentiation-associated chromosomal breakpoints in human neoplasia--a unifying model.

Authors:  S Heim; F Mitelman
Journal:  Hereditas       Date:  1986       Impact factor: 3.271

3.  Report of the Committee on Chromosome Rearrangements in Neoplasia and on Fragile Sites.

Authors:  R Berger; C D Bloomfield; G R Sutherland
Journal:  Cytogenet Cell Genet       Date:  1985

Review 4.  Specific chromosomal translocations and the genesis of B-cell-derived tumors in mice and men.

Authors:  G Klein
Journal:  Cell       Date:  1983-02       Impact factor: 41.582

Review 5.  The molecular genetics of cellular oncogenes.

Authors:  H E Varmus
Journal:  Annu Rev Genet       Date:  1984       Impact factor: 16.830

Review 6.  Clustering of aberrations to specific chromosomes in human neoplasms. IV. A survey of 1,871 cases.

Authors:  F Mitelman; G Levan
Journal:  Hereditas       Date:  1981       Impact factor: 3.271

7.  Genomic diversity correlates with clinical variation in Ph'-negative chronic myeloid leukaemia.

Authors:  C M Morris; A E Reeve; P H Fitzgerald; P E Hollings; M E Beard; D C Heaton
Journal:  Nature       Date:  1986 Mar 20-26       Impact factor: 49.962

8.  Is the chromosomal region 9q34 always involved in variants of the Ph1 translocation?

Authors:  A Hagemeijer; C R Bartram; E M Smit; A J van Agthoven; D Bootsma
Journal:  Cancer Genet Cytogenet       Date:  1984-09

9.  A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemia.

Authors:  A de Klein; A G van Kessel; G Grosveld; C R Bartram; A Hagemeijer; D Bootsma; N K Spurr; N Heisterkamp; J Groffen; J R Stephenson
Journal:  Nature       Date:  1982-12-23       Impact factor: 49.962

10.  The chromosomal basis of human neoplasia.

Authors:  J J Yunis
Journal:  Science       Date:  1983-07-15       Impact factor: 47.728

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  6 in total

Review 1.  Genes other than BRCA1 and BRCA2 involved in breast cancer susceptibility.

Authors:  M M de Jong; I M Nolte; G J te Meerman; W T A van der Graaf; J C Oosterwijk; J H Kleibeuker; M Schaapveld; E G E de Vries
Journal:  J Med Genet       Date:  2002-04       Impact factor: 6.318

Review 2.  Chromosome bands, their chromatin flavors, and their functional features.

Authors:  G P Holmquist
Journal:  Am J Hum Genet       Date:  1992-07       Impact factor: 11.025

Review 3.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

Review 4.  A model to account for the effects of oncogenes, TPA, and retinoic acid on the regulation of genes involved in metastasis.

Authors:  J Pohl; A Radler-Pohl; V Schirrmacher
Journal:  Cancer Metastasis Rev       Date:  1988-12       Impact factor: 9.264

5.  Comparison between the allelic frequency distribution of the Ha-ras 1 locus in normal individuals and patients with lymphoma, breast, and ovarian cancer.

Authors:  B Corell; B Zoll
Journal:  Hum Genet       Date:  1988-07       Impact factor: 4.132

6.  Recurrent genomic rearrangements are not at the fragile sites on chromosomes 3 and 5 in human renal cell carcinomas.

Authors:  G Kovacs; P Brusa
Journal:  Hum Genet       Date:  1988-09       Impact factor: 4.132

  6 in total

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