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The Relationship between TP53 Gene Status and Carboxylesterase 2 Expression in Human Colorectal Cancer
Irinotecan (CPT-11) is an anticancer prodrug that is activated by the carboxylesterase CES2 and has been approved for the treatment of many types of solid tumors, including colorectal cancer. Recent studies with cell lines show that CES2 expression is regulated by the tumor suppressor protein p53. H...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5831679/ https://www.ncbi.nlm.nih.gov/pubmed/29651325 http://dx.doi.org/10.1155/2018/5280736 |
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author | Ishimine, Momoko Lee, Hyeon-Cheol Nakaoka, Hirofumi Orita, Hajime Kobayashi, Toshiyuki Mizuguchi, Konomi Endo, Mikumi Inoue, Ituro Sato, Koichi Yokomizo, Takehiko |
author_facet | Ishimine, Momoko Lee, Hyeon-Cheol Nakaoka, Hirofumi Orita, Hajime Kobayashi, Toshiyuki Mizuguchi, Konomi Endo, Mikumi Inoue, Ituro Sato, Koichi Yokomizo, Takehiko |
author_sort | Ishimine, Momoko |
collection | PubMed |
description | Irinotecan (CPT-11) is an anticancer prodrug that is activated by the carboxylesterase CES2 and has been approved for the treatment of many types of solid tumors, including colorectal cancer. Recent studies with cell lines show that CES2 expression is regulated by the tumor suppressor protein p53. However, clinical evidence for this regulatory mechanism in cancer is lacking. In this study, we examined the relationship between TP53 gene status and CES2 expression in human colorectal cancer. Most colorectal cancer specimens (70%; 26 of 37) showed lower CES2 mRNA levels (≥1.5-fold lower) than the adjacent normal tissue, and only 30% (12 of 37) showed similar (<1.5-fold lower) or higher CES2 mRNA levels. However, TP53 gene sequencing revealed no relationship between CES2 downregulation and TP53 mutational status. Moreover, while colorectal cancer cells expressing wild-type p53 exhibited p53-dependent upregulation of CES2, PRIMA-1(MET), a drug that restores the transcriptional activity of mutant p53, failed to upregulate CES2 expression in cells with TP53 missense mutations. These results, taken together, suggest that CES2 mRNA expression is decreased in human colorectal cancer independently of p53. |
format | Online Article Text |
id | pubmed-5831679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-58316792018-04-12 The Relationship between TP53 Gene Status and Carboxylesterase 2 Expression in Human Colorectal Cancer Ishimine, Momoko Lee, Hyeon-Cheol Nakaoka, Hirofumi Orita, Hajime Kobayashi, Toshiyuki Mizuguchi, Konomi Endo, Mikumi Inoue, Ituro Sato, Koichi Yokomizo, Takehiko Dis Markers Research Article Irinotecan (CPT-11) is an anticancer prodrug that is activated by the carboxylesterase CES2 and has been approved for the treatment of many types of solid tumors, including colorectal cancer. Recent studies with cell lines show that CES2 expression is regulated by the tumor suppressor protein p53. However, clinical evidence for this regulatory mechanism in cancer is lacking. In this study, we examined the relationship between TP53 gene status and CES2 expression in human colorectal cancer. Most colorectal cancer specimens (70%; 26 of 37) showed lower CES2 mRNA levels (≥1.5-fold lower) than the adjacent normal tissue, and only 30% (12 of 37) showed similar (<1.5-fold lower) or higher CES2 mRNA levels. However, TP53 gene sequencing revealed no relationship between CES2 downregulation and TP53 mutational status. Moreover, while colorectal cancer cells expressing wild-type p53 exhibited p53-dependent upregulation of CES2, PRIMA-1(MET), a drug that restores the transcriptional activity of mutant p53, failed to upregulate CES2 expression in cells with TP53 missense mutations. These results, taken together, suggest that CES2 mRNA expression is decreased in human colorectal cancer independently of p53. Hindawi 2018-01-31 /pmc/articles/PMC5831679/ /pubmed/29651325 http://dx.doi.org/10.1155/2018/5280736 Text en Copyright © 2018 Momoko Ishimine et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Ishimine, Momoko Lee, Hyeon-Cheol Nakaoka, Hirofumi Orita, Hajime Kobayashi, Toshiyuki Mizuguchi, Konomi Endo, Mikumi Inoue, Ituro Sato, Koichi Yokomizo, Takehiko The Relationship between TP53 Gene Status and Carboxylesterase 2 Expression in Human Colorectal Cancer |
title | The Relationship between TP53 Gene Status and Carboxylesterase 2 Expression in Human Colorectal Cancer |
title_full | The Relationship between TP53 Gene Status and Carboxylesterase 2 Expression in Human Colorectal Cancer |
title_fullStr | The Relationship between TP53 Gene Status and Carboxylesterase 2 Expression in Human Colorectal Cancer |
title_full_unstemmed | The Relationship between TP53 Gene Status and Carboxylesterase 2 Expression in Human Colorectal Cancer |
title_short | The Relationship between TP53 Gene Status and Carboxylesterase 2 Expression in Human Colorectal Cancer |
title_sort | relationship between tp53 gene status and carboxylesterase 2 expression in human colorectal cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5831679/ https://www.ncbi.nlm.nih.gov/pubmed/29651325 http://dx.doi.org/10.1155/2018/5280736 |
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