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Higher Frequency of Point Mutations in the c‐K‐ras2 Gene in Human Colorectal Adenomas with Severe Atypia than in Carcinomas

Human colorectal carcinomas may be induced from adenomas or they may occur de novo. To examine which is the main pathway, we analyzed point mutations at codon 12 in the c‐K‐ras 2 gene in 73 colorectal carcinomas, 13 metastatic tumors, 72 adenomas and 30 normal tissues. The c‐K‐ras 2 codon 12 mutatio...

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Autores principales: Ando, Masayuki, Maruyama, Michio, Oto, Michiei, Takemura, Katsuji, Endo, Mitsuo, Yuasa, Yasuhito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1991
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918406/
https://www.ncbi.nlm.nih.gov/pubmed/1708754
http://dx.doi.org/10.1111/j.1349-7006.1991.tb01836.x
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author Ando, Masayuki
Maruyama, Michio
Oto, Michiei
Takemura, Katsuji
Endo, Mitsuo
Yuasa, Yasuhito
author_facet Ando, Masayuki
Maruyama, Michio
Oto, Michiei
Takemura, Katsuji
Endo, Mitsuo
Yuasa, Yasuhito
author_sort Ando, Masayuki
collection PubMed
description Human colorectal carcinomas may be induced from adenomas or they may occur de novo. To examine which is the main pathway, we analyzed point mutations at codon 12 in the c‐K‐ras 2 gene in 73 colorectal carcinomas, 13 metastatic tumors, 72 adenomas and 30 normal tissues. The c‐K‐ras 2 codon 12 mutation frequency was 0/30 in normal tissues, 0/17 in adenomas with mild atypia, 3/37 (8.1%) in adenomas with moderate atypia, 15/18 (83.3%) in adenomas with severe atypia, 19/73 (26.0%) in primary carcinomas and 3/13 (23.1%) in metastatic tumors. The mutation frequency in adenomas with severe atypia was much higher than that in carcinomas. These results indicate that many colorectal carcinomas may not be induced through adenomas with severe atypia.
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spelling pubmed-59184062018-05-11 Higher Frequency of Point Mutations in the c‐K‐ras2 Gene in Human Colorectal Adenomas with Severe Atypia than in Carcinomas Ando, Masayuki Maruyama, Michio Oto, Michiei Takemura, Katsuji Endo, Mitsuo Yuasa, Yasuhito Jpn J Cancer Res Rapid Communication Human colorectal carcinomas may be induced from adenomas or they may occur de novo. To examine which is the main pathway, we analyzed point mutations at codon 12 in the c‐K‐ras 2 gene in 73 colorectal carcinomas, 13 metastatic tumors, 72 adenomas and 30 normal tissues. The c‐K‐ras 2 codon 12 mutation frequency was 0/30 in normal tissues, 0/17 in adenomas with mild atypia, 3/37 (8.1%) in adenomas with moderate atypia, 15/18 (83.3%) in adenomas with severe atypia, 19/73 (26.0%) in primary carcinomas and 3/13 (23.1%) in metastatic tumors. The mutation frequency in adenomas with severe atypia was much higher than that in carcinomas. These results indicate that many colorectal carcinomas may not be induced through adenomas with severe atypia. Blackwell Publishing Ltd 1991-03 /pmc/articles/PMC5918406/ /pubmed/1708754 http://dx.doi.org/10.1111/j.1349-7006.1991.tb01836.x Text en
spellingShingle Rapid Communication
Ando, Masayuki
Maruyama, Michio
Oto, Michiei
Takemura, Katsuji
Endo, Mitsuo
Yuasa, Yasuhito
Higher Frequency of Point Mutations in the c‐K‐ras2 Gene in Human Colorectal Adenomas with Severe Atypia than in Carcinomas
title Higher Frequency of Point Mutations in the c‐K‐ras2 Gene in Human Colorectal Adenomas with Severe Atypia than in Carcinomas
title_full Higher Frequency of Point Mutations in the c‐K‐ras2 Gene in Human Colorectal Adenomas with Severe Atypia than in Carcinomas
title_fullStr Higher Frequency of Point Mutations in the c‐K‐ras2 Gene in Human Colorectal Adenomas with Severe Atypia than in Carcinomas
title_full_unstemmed Higher Frequency of Point Mutations in the c‐K‐ras2 Gene in Human Colorectal Adenomas with Severe Atypia than in Carcinomas
title_short Higher Frequency of Point Mutations in the c‐K‐ras2 Gene in Human Colorectal Adenomas with Severe Atypia than in Carcinomas
title_sort higher frequency of point mutations in the c‐k‐ras2 gene in human colorectal adenomas with severe atypia than in carcinomas
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918406/
https://www.ncbi.nlm.nih.gov/pubmed/1708754
http://dx.doi.org/10.1111/j.1349-7006.1991.tb01836.x
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