TY - JOUR
T1 - Molecular genotyping for N‐acetylation polymorphism in Japanese patients with colorectal cancer
AU - Shibuta, Kenji
AU - Nakashima, Tadasu
AU - Abe, Masako
AU - Mashimo, Masami
AU - Mori, Masaki
AU - Ueo, Hiroaki
AU - Akiyoshi, Tsuyoshi
AU - Sugimachi, Keizo
AU - Suzuki, Tomokazu
PY - 1994/12/15
Y1 - 1994/12/15
N2 - Background. N‐acetylation polymorphism has been documented as a representative pharmacogenetic trait, and also has been implicated ecogenetically in an individual's susceptibility to cancer. However, there still remains controversy concerning the association between colorectal cancer and N‐acetylation polymorphism. Methods. A newly established molecular genotyping method using polymerase chain reaction‐based restriction fragment length polymorphism to analyze the distribution of polymorphism in a large group of Japanese patients with colorectal cancer was used. Results. Based on an analysis of 234 Japanese patients with colorectal cancer and 329 healthy control subjects, no significant difference was observed in either the distribution of acetylator phenotypes or of allele frequencies between the two groups. In addition, no significant difference in their distribution was found based on the age at which cancer was first detected, the location of tumors, or the histopathologic features. Conclusions. N‐acetylation polymorphism does not appear to be implicated crucially as a genetic trait affecting an individual's susceptibility to colorectal cancer.
AB - Background. N‐acetylation polymorphism has been documented as a representative pharmacogenetic trait, and also has been implicated ecogenetically in an individual's susceptibility to cancer. However, there still remains controversy concerning the association between colorectal cancer and N‐acetylation polymorphism. Methods. A newly established molecular genotyping method using polymerase chain reaction‐based restriction fragment length polymorphism to analyze the distribution of polymorphism in a large group of Japanese patients with colorectal cancer was used. Results. Based on an analysis of 234 Japanese patients with colorectal cancer and 329 healthy control subjects, no significant difference was observed in either the distribution of acetylator phenotypes or of allele frequencies between the two groups. In addition, no significant difference in their distribution was found based on the age at which cancer was first detected, the location of tumors, or the histopathologic features. Conclusions. N‐acetylation polymorphism does not appear to be implicated crucially as a genetic trait affecting an individual's susceptibility to colorectal cancer.
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U2 - 10.1002/1097-0142(19941215)74:12<3108::AID-CNCR2820741208>3.0.CO;2-M
DO - 10.1002/1097-0142(19941215)74:12<3108::AID-CNCR2820741208>3.0.CO;2-M
M3 - Article
C2 - 7982175
AN - SCOPUS:0028171420
SN - 0008-543X
VL - 74
SP - 3108
EP - 3112
JO - Cancer
JF - Cancer
IS - 12
ER -