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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
1995
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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. |
format | Online Article Text |
id | pubmed-5920883 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1995 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
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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