Cargando…
A Single Nucleotide Polymorphism in the Matrix Metalloproteinase‐1 Promoter in Endometrial Carcinomas
Recent studies demonstrated that a single guanine insertion polymorphism in a matrix metalloprotease‐1 promoter created an Ets binding site and affected the elevation of the transcriptional level of matrix metalloproteinase‐1 (MMP‐1). Furthermore, in tumor cell lines derived from melanoma and breast...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2000
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926401/ https://www.ncbi.nlm.nih.gov/pubmed/10874213 http://dx.doi.org/10.1111/j.1349-7006.2000.tb00989.x |
_version_ | 1783318898411569152 |
---|---|
author | Nishioka, Yoshihiro Kobayashi, Kanji Sagae, Satoru Ishioka, Shin‐ichi Nishikawa, Akira Matsushima, Mieko Kanamori, Yasunobu Minaguchi, Takeo Nakamura, Yusuke Tokino, Takashi Kudo, Ryuichi |
author_facet | Nishioka, Yoshihiro Kobayashi, Kanji Sagae, Satoru Ishioka, Shin‐ichi Nishikawa, Akira Matsushima, Mieko Kanamori, Yasunobu Minaguchi, Takeo Nakamura, Yusuke Tokino, Takashi Kudo, Ryuichi |
author_sort | Nishioka, Yoshihiro |
collection | PubMed |
description | Recent studies demonstrated that a single guanine insertion polymorphism in a matrix metalloprotease‐1 promoter created an Ets binding site and affected the elevation of the transcriptional level of matrix metalloproteinase‐1 (MMP‐1). Furthermore, in tumor cell lines derived from melanoma and breast cancer, the incidence of the 2G/2G genotype was significantly higher than that in the normal population. To evaluate the contribution of this polymorphism in endometrial carcinomas, we genotyped 100 endometrial carcinomas and then analyzed immunoexpression of MMP‐1 in these carcinomas. We found that endometrial carcinoma patients showed a significantly higher rate of 1G/2G or 2G/2G genotype than control individuals, and that tumors containing the 2G allele(a) expressed MMP‐1 protein more frequently than those with 1G/1G genotype. Therefore, the single nucleotide polymorphism at the MMP‐1 promoter affected the expression level of the MMP‐1 protein, which may result in the association with more aggressive character in endometrial carcinoma. Our result suggests that the presence of 2G polymorphism at the MMP‐1 promoter may be one of the risk factors for the development and/or progression of endometrial carcinoma. |
format | Online Article Text |
id | pubmed-5926401 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-59264012018-05-11 A Single Nucleotide Polymorphism in the Matrix Metalloproteinase‐1 Promoter in Endometrial Carcinomas Nishioka, Yoshihiro Kobayashi, Kanji Sagae, Satoru Ishioka, Shin‐ichi Nishikawa, Akira Matsushima, Mieko Kanamori, Yasunobu Minaguchi, Takeo Nakamura, Yusuke Tokino, Takashi Kudo, Ryuichi Jpn J Cancer Res Article Recent studies demonstrated that a single guanine insertion polymorphism in a matrix metalloprotease‐1 promoter created an Ets binding site and affected the elevation of the transcriptional level of matrix metalloproteinase‐1 (MMP‐1). Furthermore, in tumor cell lines derived from melanoma and breast cancer, the incidence of the 2G/2G genotype was significantly higher than that in the normal population. To evaluate the contribution of this polymorphism in endometrial carcinomas, we genotyped 100 endometrial carcinomas and then analyzed immunoexpression of MMP‐1 in these carcinomas. We found that endometrial carcinoma patients showed a significantly higher rate of 1G/2G or 2G/2G genotype than control individuals, and that tumors containing the 2G allele(a) expressed MMP‐1 protein more frequently than those with 1G/1G genotype. Therefore, the single nucleotide polymorphism at the MMP‐1 promoter affected the expression level of the MMP‐1 protein, which may result in the association with more aggressive character in endometrial carcinoma. Our result suggests that the presence of 2G polymorphism at the MMP‐1 promoter may be one of the risk factors for the development and/or progression of endometrial carcinoma. Blackwell Publishing Ltd 2000-06 /pmc/articles/PMC5926401/ /pubmed/10874213 http://dx.doi.org/10.1111/j.1349-7006.2000.tb00989.x Text en |
spellingShingle | Article Nishioka, Yoshihiro Kobayashi, Kanji Sagae, Satoru Ishioka, Shin‐ichi Nishikawa, Akira Matsushima, Mieko Kanamori, Yasunobu Minaguchi, Takeo Nakamura, Yusuke Tokino, Takashi Kudo, Ryuichi A Single Nucleotide Polymorphism in the Matrix Metalloproteinase‐1 Promoter in Endometrial Carcinomas |
title | A Single Nucleotide Polymorphism in the Matrix Metalloproteinase‐1 Promoter in Endometrial Carcinomas |
title_full | A Single Nucleotide Polymorphism in the Matrix Metalloproteinase‐1 Promoter in Endometrial Carcinomas |
title_fullStr | A Single Nucleotide Polymorphism in the Matrix Metalloproteinase‐1 Promoter in Endometrial Carcinomas |
title_full_unstemmed | A Single Nucleotide Polymorphism in the Matrix Metalloproteinase‐1 Promoter in Endometrial Carcinomas |
title_short | A Single Nucleotide Polymorphism in the Matrix Metalloproteinase‐1 Promoter in Endometrial Carcinomas |
title_sort | single nucleotide polymorphism in the matrix metalloproteinase‐1 promoter in endometrial carcinomas |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926401/ https://www.ncbi.nlm.nih.gov/pubmed/10874213 http://dx.doi.org/10.1111/j.1349-7006.2000.tb00989.x |
work_keys_str_mv | AT nishiokayoshihiro asinglenucleotidepolymorphisminthematrixmetalloproteinase1promoterinendometrialcarcinomas AT kobayashikanji asinglenucleotidepolymorphisminthematrixmetalloproteinase1promoterinendometrialcarcinomas AT sagaesatoru asinglenucleotidepolymorphisminthematrixmetalloproteinase1promoterinendometrialcarcinomas AT ishiokashinichi asinglenucleotidepolymorphisminthematrixmetalloproteinase1promoterinendometrialcarcinomas AT nishikawaakira asinglenucleotidepolymorphisminthematrixmetalloproteinase1promoterinendometrialcarcinomas AT matsushimamieko asinglenucleotidepolymorphisminthematrixmetalloproteinase1promoterinendometrialcarcinomas AT kanamoriyasunobu asinglenucleotidepolymorphisminthematrixmetalloproteinase1promoterinendometrialcarcinomas AT minaguchitakeo asinglenucleotidepolymorphisminthematrixmetalloproteinase1promoterinendometrialcarcinomas AT nakamurayusuke asinglenucleotidepolymorphisminthematrixmetalloproteinase1promoterinendometrialcarcinomas AT tokinotakashi asinglenucleotidepolymorphisminthematrixmetalloproteinase1promoterinendometrialcarcinomas AT kudoryuichi asinglenucleotidepolymorphisminthematrixmetalloproteinase1promoterinendometrialcarcinomas AT nishiokayoshihiro singlenucleotidepolymorphisminthematrixmetalloproteinase1promoterinendometrialcarcinomas AT kobayashikanji singlenucleotidepolymorphisminthematrixmetalloproteinase1promoterinendometrialcarcinomas AT sagaesatoru singlenucleotidepolymorphisminthematrixmetalloproteinase1promoterinendometrialcarcinomas AT ishiokashinichi singlenucleotidepolymorphisminthematrixmetalloproteinase1promoterinendometrialcarcinomas AT nishikawaakira singlenucleotidepolymorphisminthematrixmetalloproteinase1promoterinendometrialcarcinomas AT matsushimamieko singlenucleotidepolymorphisminthematrixmetalloproteinase1promoterinendometrialcarcinomas AT kanamoriyasunobu singlenucleotidepolymorphisminthematrixmetalloproteinase1promoterinendometrialcarcinomas AT minaguchitakeo singlenucleotidepolymorphisminthematrixmetalloproteinase1promoterinendometrialcarcinomas AT nakamurayusuke singlenucleotidepolymorphisminthematrixmetalloproteinase1promoterinendometrialcarcinomas AT tokinotakashi singlenucleotidepolymorphisminthematrixmetalloproteinase1promoterinendometrialcarcinomas AT kudoryuichi singlenucleotidepolymorphisminthematrixmetalloproteinase1promoterinendometrialcarcinomas |