Loss of heterozygosity at autosomal and X-linked loci during tumor progression in a patient with melanoma Journal Article


Authors: Dracopoli, N. C.; Alhadeff, B.; Houghton, A. N.; Old, L. J.
Article Title: Loss of heterozygosity at autosomal and X-linked loci during tumor progression in a patient with melanoma
Abstract: Restriction fragment length polymorphisms at 61 autosomal and 7 X-linked loci were screened for heterozygosity in cell lines derived from 6 independent metastases and autologous B-cells from a patient with melanoma. Segregations resulting in the loss of heterozygosity were detected in the tumor cells at 8 of 16 autosomes with at least 1 informative locus and at the 3 informative X-linked loci. With a single exception, karyotypic abnormalities were not detected in the region of loci where loss of heterozygosity had been detected. Three patterns of loss were identified: (a) unique segregations in cells from a single metastasis; (b) segregation of the same alleles in different subsets of metastases; and (c) identical segregations in all 6 metastases. The monoclonal derivation of the 6 metastases is supported by the inactivation of the same X-chromosome and the presence of identical segregations at loci on chromosomes 9 and X. Analysis of the patterns of segregation in the metastatic tumor cells permitted the development of a genealogy of tumor progression in this patient and the development of a model of tumor progression which describes the accumulation of selectively neutral and advantageous segregations in metastatic tumor cells. © 1987, American Association for Cancer Research. All rights reserved.
Keywords: aged; case report; comparative study; melanoma; models, biological; skin neoplasms; cell line; b-lymphocytes; selection (genetics); heterozygosity; chromosome aberrations; tumor growth; aneuploidy; clone cells; genetic markers; abdominal neoplasms; polymorphism, restriction fragment length; human; female; priority journal; support, non-u.s. gov't; support, u.s. gov't, p.h.s.; dosage compensation (genetics)
Journal Title: Cancer Research
Volume: 47
Issue: 15
ISSN: 0008-5472
Publisher: American Association for Cancer Research  
Date Published: 1987-08-01
Start Page: 3995
End Page: 4000
Language: English
PUBMED: 2886213
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 5 February 2021 -- Source: Scopus
Citation Impact
MSK Authors
  1. Alan N Houghton
    364 Houghton
  2. Lloyd J Old
    593 Old