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Frequent Allelic Imbalance on Chromosome 18q21 in Early Superficial Colorectal Cancers
Genetic alterations in early superficial colorectal cancers have rarely been reported. In the present study, we searched for alterations in the APC and p53 genes in 27 superficial (20 depressed and 7 elevated) and 21 protruding colorectal cancers with submucosal invasion by means of PCR‐single stran...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
1999
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926027/ https://www.ncbi.nlm.nih.gov/pubmed/10665650 http://dx.doi.org/10.1111/j.1349-7006.1999.tb00716.x |
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author | Akiyama, Yoshimitsu Arai, Takehiro Nagasaki, Hiromi Yagi, Osmar Kenji Nakahata, Atsuko Nakajima, Tomoko Ohkura, Yasuo Iwai, Takehisa Saitoh, Kiyoshi Yuasa, Yasuhito |
author_facet | Akiyama, Yoshimitsu Arai, Takehiro Nagasaki, Hiromi Yagi, Osmar Kenji Nakahata, Atsuko Nakajima, Tomoko Ohkura, Yasuo Iwai, Takehisa Saitoh, Kiyoshi Yuasa, Yasuhito |
author_sort | Akiyama, Yoshimitsu |
collection | PubMed |
description | Genetic alterations in early superficial colorectal cancers have rarely been reported. In the present study, we searched for alterations in the APC and p53 genes in 27 superficial (20 depressed and 7 elevated) and 21 protruding colorectal cancers with submucosal invasion by means of PCR‐single strand conformation polymorphism. Allelic imbalance (AI) on five loci, i.e., 1p34‐36, 8p21‐22, 14q32, 18q21 and 22q12‐13, was also analyzed. Since a high incidence of 18q21 AI was detected in the superficial depressed cases, we further screened for alterations in Smad2, Smad4 and DCC. APC alterations were observed in three superficial depressed, one superficial elevated, and 11 protruding colorectal cancers, indicating that the frequency of APC alterations in superficial depressed cases was significantly lower than that in the protruding ones. There was no significant association between p53 alterations and macroscopic types. AI on 18q21 (13/20, 65%) was much higher than those on the other four loci in the superficial depressed cases. Moreover, the frequency of 18q21 AI in the superficial depressed cases was significantly higher than that in the protruding ones. Smad4 alterations were only detected in 1 of the 13 superficial depressed and 3 of the 17 protruding cases, while Smad2 and DCC alterations were not detected in any case examined. These data suggest that the carcinogenetic pathways of protruding and superficial depressed colorectal cancers are different, and that alterations of tumor suppressor gene(s) located on 18q21 other than Smad2, Smad4 and DCC might be associated with most superficial depressed colorectal cancers. |
format | Online Article Text |
id | pubmed-5926027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1999 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-59260272018-05-11 Frequent Allelic Imbalance on Chromosome 18q21 in Early Superficial Colorectal Cancers Akiyama, Yoshimitsu Arai, Takehiro Nagasaki, Hiromi Yagi, Osmar Kenji Nakahata, Atsuko Nakajima, Tomoko Ohkura, Yasuo Iwai, Takehisa Saitoh, Kiyoshi Yuasa, Yasuhito Jpn J Cancer Res Article Genetic alterations in early superficial colorectal cancers have rarely been reported. In the present study, we searched for alterations in the APC and p53 genes in 27 superficial (20 depressed and 7 elevated) and 21 protruding colorectal cancers with submucosal invasion by means of PCR‐single strand conformation polymorphism. Allelic imbalance (AI) on five loci, i.e., 1p34‐36, 8p21‐22, 14q32, 18q21 and 22q12‐13, was also analyzed. Since a high incidence of 18q21 AI was detected in the superficial depressed cases, we further screened for alterations in Smad2, Smad4 and DCC. APC alterations were observed in three superficial depressed, one superficial elevated, and 11 protruding colorectal cancers, indicating that the frequency of APC alterations in superficial depressed cases was significantly lower than that in the protruding ones. There was no significant association between p53 alterations and macroscopic types. AI on 18q21 (13/20, 65%) was much higher than those on the other four loci in the superficial depressed cases. Moreover, the frequency of 18q21 AI in the superficial depressed cases was significantly higher than that in the protruding ones. Smad4 alterations were only detected in 1 of the 13 superficial depressed and 3 of the 17 protruding cases, while Smad2 and DCC alterations were not detected in any case examined. These data suggest that the carcinogenetic pathways of protruding and superficial depressed colorectal cancers are different, and that alterations of tumor suppressor gene(s) located on 18q21 other than Smad2, Smad4 and DCC might be associated with most superficial depressed colorectal cancers. Blackwell Publishing Ltd 1999-12 /pmc/articles/PMC5926027/ /pubmed/10665650 http://dx.doi.org/10.1111/j.1349-7006.1999.tb00716.x Text en |
spellingShingle | Article Akiyama, Yoshimitsu Arai, Takehiro Nagasaki, Hiromi Yagi, Osmar Kenji Nakahata, Atsuko Nakajima, Tomoko Ohkura, Yasuo Iwai, Takehisa Saitoh, Kiyoshi Yuasa, Yasuhito Frequent Allelic Imbalance on Chromosome 18q21 in Early Superficial Colorectal Cancers |
title | Frequent Allelic Imbalance on Chromosome 18q21 in Early Superficial Colorectal Cancers |
title_full | Frequent Allelic Imbalance on Chromosome 18q21 in Early Superficial Colorectal Cancers |
title_fullStr | Frequent Allelic Imbalance on Chromosome 18q21 in Early Superficial Colorectal Cancers |
title_full_unstemmed | Frequent Allelic Imbalance on Chromosome 18q21 in Early Superficial Colorectal Cancers |
title_short | Frequent Allelic Imbalance on Chromosome 18q21 in Early Superficial Colorectal Cancers |
title_sort | frequent allelic imbalance on chromosome 18q21 in early superficial colorectal cancers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926027/ https://www.ncbi.nlm.nih.gov/pubmed/10665650 http://dx.doi.org/10.1111/j.1349-7006.1999.tb00716.x |
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