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Mutational Analysis of CDKN2 (CDK4I/MTS1) Gene in Tissues and Cell Lines of Human Prostate Cancer

To study mutation of the CDKN2 gene in prostate cancer, samples from 51 Japanese patients and four human prostate cancer cell lines were examined by single‐strand conformation polymorphism analysis and direct sequencing. Only one out of 51 (2%) patients revealed a mutation, which was a 24 bp deletio...

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Detalles Bibliográficos
Autores principales: Komiya, Akira, Suzuki, Hiroyoshi, Aida, Sara, Yatani, Ryuichi, Shimazaki, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1995
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920883/
https://www.ncbi.nlm.nih.gov/pubmed/7559077
http://dx.doi.org/10.1111/j.1349-7006.1995.tb02443.x
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author Komiya, Akira
Suzuki, Hiroyoshi
Aida, Sara
Yatani, Ryuichi
Shimazaki, Jun
author_facet Komiya, Akira
Suzuki, Hiroyoshi
Aida, Sara
Yatani, Ryuichi
Shimazaki, Jun
author_sort Komiya, Akira
collection PubMed
description To study mutation of the CDKN2 gene in prostate cancer, samples from 51 Japanese patients and four human prostate cancer cell lines were examined by single‐strand conformation polymorphism analysis and direct sequencing. Only one out of 51 (2%) patients revealed a mutation, which was a 24 bp deletion from the 5′‐untranslated region to codon 3, resulting in loss of the initiation site. One of the four cell lines revealed a missense mutation, a GAC→TAC (Asp→Tyr) at codon 84. These results indicate that mutation of the CDKN2 gene is rare in prostate cancer and thus does not contribute significantly to the pathogenesis of human prostate cancer. Prostate cancer cell lines may acquire more frequent abnormality of the CDKN2 gene than tumor tissues.
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spelling pubmed-59208832018-05-11 Mutational Analysis of CDKN2 (CDK4I/MTS1) Gene in Tissues and Cell Lines of Human Prostate Cancer Komiya, Akira Suzuki, Hiroyoshi Aida, Sara Yatani, Ryuichi Shimazaki, Jun Jpn J Cancer Res Rapid Communication To study mutation of the CDKN2 gene in prostate cancer, samples from 51 Japanese patients and four human prostate cancer cell lines were examined by single‐strand conformation polymorphism analysis and direct sequencing. Only one out of 51 (2%) patients revealed a mutation, which was a 24 bp deletion from the 5′‐untranslated region to codon 3, resulting in loss of the initiation site. One of the four cell lines revealed a missense mutation, a GAC→TAC (Asp→Tyr) at codon 84. These results indicate that mutation of the CDKN2 gene is rare in prostate cancer and thus does not contribute significantly to the pathogenesis of human prostate cancer. Prostate cancer cell lines may acquire more frequent abnormality of the CDKN2 gene than tumor tissues. Blackwell Publishing Ltd 1995-07 /pmc/articles/PMC5920883/ /pubmed/7559077 http://dx.doi.org/10.1111/j.1349-7006.1995.tb02443.x Text en
spellingShingle Rapid Communication
Komiya, Akira
Suzuki, Hiroyoshi
Aida, Sara
Yatani, Ryuichi
Shimazaki, Jun
Mutational Analysis of CDKN2 (CDK4I/MTS1) Gene in Tissues and Cell Lines of Human Prostate Cancer
title Mutational Analysis of CDKN2 (CDK4I/MTS1) Gene in Tissues and Cell Lines of Human Prostate Cancer
title_full Mutational Analysis of CDKN2 (CDK4I/MTS1) Gene in Tissues and Cell Lines of Human Prostate Cancer
title_fullStr Mutational Analysis of CDKN2 (CDK4I/MTS1) Gene in Tissues and Cell Lines of Human Prostate Cancer
title_full_unstemmed Mutational Analysis of CDKN2 (CDK4I/MTS1) Gene in Tissues and Cell Lines of Human Prostate Cancer
title_short Mutational Analysis of CDKN2 (CDK4I/MTS1) Gene in Tissues and Cell Lines of Human Prostate Cancer
title_sort mutational analysis of cdkn2 (cdk4i/mts1) gene in tissues and cell lines of human prostate cancer
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920883/
https://www.ncbi.nlm.nih.gov/pubmed/7559077
http://dx.doi.org/10.1111/j.1349-7006.1995.tb02443.x
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