MYCL genotypes and loss of heterozygosity in non-small-cell lung cancer.

Some studies have suggested that the S allele of the MYCL oncogene, which results from an intragenic EcoRI restriction fragment length polymorphism (RFLP), may be associated with cancer susceptibility. In addition, this allele has also been linked to metastases and adverse survival in certain cancer...

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Main Authors: Fong, K. M., Kida, Y., Zimmerman, P. V., Smith, P. J.
Format: Online
Language:English
Published: Nature Publishing Group 1996
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2074830/
id pubmed-2074830
recordtype oai_dc
spelling pubmed-20748302009-09-10 MYCL genotypes and loss of heterozygosity in non-small-cell lung cancer. Fong, K. M. Kida, Y. Zimmerman, P. V. Smith, P. J. Research Article Some studies have suggested that the S allele of the MYCL oncogene, which results from an intragenic EcoRI restriction fragment length polymorphism (RFLP), may be associated with cancer susceptibility. In addition, this allele has also been linked to metastases and adverse survival in certain cancers, although studies of lung cancer patients from different populations have yielded controversial results. We studied 108 cases of surgical resected non-small-cell lung cancer (NSCLC) and found no evidence that MYCL genotypes were associated with tumour progression or a worse prognosis. However, the presence of loss of heterozygosity (LOH) at this chromosome 1p32 locus correlated significantly with regional lymph node involvement, as well as advanced TNM stage. These data indicate the existence of a chromosome 1p candidate tumour-suppressor gene(s), possibly in linkage disequilibrium with the EcoRI RFLP in specific populations, which appears to play a role in determining tumour progression in NSCLC. Refined mapping of the critical region of loss should help attempts to identify and clone the candidate gene. Nature Publishing Group 1996-12 /pmc/articles/PMC2074830/ /pubmed/8980399 Text en
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Fong, K. M.
Kida, Y.
Zimmerman, P. V.
Smith, P. J.
spellingShingle Fong, K. M.
Kida, Y.
Zimmerman, P. V.
Smith, P. J.
MYCL genotypes and loss of heterozygosity in non-small-cell lung cancer.
author_facet Fong, K. M.
Kida, Y.
Zimmerman, P. V.
Smith, P. J.
author_sort Fong, K. M.
title MYCL genotypes and loss of heterozygosity in non-small-cell lung cancer.
title_short MYCL genotypes and loss of heterozygosity in non-small-cell lung cancer.
title_full MYCL genotypes and loss of heterozygosity in non-small-cell lung cancer.
title_fullStr MYCL genotypes and loss of heterozygosity in non-small-cell lung cancer.
title_full_unstemmed MYCL genotypes and loss of heterozygosity in non-small-cell lung cancer.
title_sort mycl genotypes and loss of heterozygosity in non-small-cell lung cancer.
description Some studies have suggested that the S allele of the MYCL oncogene, which results from an intragenic EcoRI restriction fragment length polymorphism (RFLP), may be associated with cancer susceptibility. In addition, this allele has also been linked to metastases and adverse survival in certain cancers, although studies of lung cancer patients from different populations have yielded controversial results. We studied 108 cases of surgical resected non-small-cell lung cancer (NSCLC) and found no evidence that MYCL genotypes were associated with tumour progression or a worse prognosis. However, the presence of loss of heterozygosity (LOH) at this chromosome 1p32 locus correlated significantly with regional lymph node involvement, as well as advanced TNM stage. These data indicate the existence of a chromosome 1p candidate tumour-suppressor gene(s), possibly in linkage disequilibrium with the EcoRI RFLP in specific populations, which appears to play a role in determining tumour progression in NSCLC. Refined mapping of the critical region of loss should help attempts to identify and clone the candidate gene.
publisher Nature Publishing Group
publishDate 1996
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2074830/
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