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Infrequent Mutation of Lysophosphatidic Acid Receptor-1 Gene in Hamster Pancreatic Duct Adenocarcinomas and Established Cell Lines
To evaluate the involvement of lysophosphatidic acid receptor-1 (LPA1) gene alteration in pancreatic carcinogenesis, we investigated mutations in the LPA1 gene in hamster pancreatic duct adenocarcinomas (PDAs) and established cell lines. Female Syrian golden hamsters received 30 mg/kg of N-nitrosobi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Japanese Society of Toxicologic Pathology
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3246023/ https://www.ncbi.nlm.nih.gov/pubmed/22271981 http://dx.doi.org/10.1293/tox.22.89 |
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author | Tsujiuchi, Toshifumi Furukawa, Mami Obo, Yumi Yamasaki, Ayako Hotta, Mayuko Kusunoki, Chie Suyama, Naoko Mori, Toshio Honoki, Kanya Fukushima, Nobuyuki |
author_facet | Tsujiuchi, Toshifumi Furukawa, Mami Obo, Yumi Yamasaki, Ayako Hotta, Mayuko Kusunoki, Chie Suyama, Naoko Mori, Toshio Honoki, Kanya Fukushima, Nobuyuki |
author_sort | Tsujiuchi, Toshifumi |
collection | PubMed |
description | To evaluate the involvement of lysophosphatidic acid receptor-1 (LPA1) gene alteration in pancreatic carcinogenesis, we investigated mutations in the LPA1 gene in hamster pancreatic duct adenocarcinomas (PDAs) and established cell lines. Female Syrian golden hamsters received 30 mg/kg of N-nitrosobis(2-oxopropyl)amine (BOP) followed by repeated exposure to an augmentation pressure regimen consisting of a choline-deficient diet combined with DL-ethionine and then L-methionine and a further administration of 20 mg/kg BOP. A total of 10 PDAs obtained 10 weeks after beginning the experiment and three cell lines established from subcutaneously transplantable PDAs in syngeneic hamsters were examined for mutations using reverse transcription-polymerase chain reaction-single strand conformation polymorphism (RT-PCR-SSCP) analysis. A mutation was detected in only one PDA (1/10, 10%) in the form of a GGA to GTA (Gly to Val) transversion at codon 355, and no mutations were detected in the three cell lines. These results suggest that the LPA1 gene mutation may play roles in a limited fraction of BOP-induced pancreatic duct carcinogenesis in hamsters. |
format | Online Article Text |
id | pubmed-3246023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | The Japanese Society of Toxicologic Pathology |
record_format | MEDLINE/PubMed |
spelling | pubmed-32460232012-01-23 Infrequent Mutation of Lysophosphatidic Acid Receptor-1 Gene in Hamster Pancreatic Duct Adenocarcinomas and Established Cell Lines Tsujiuchi, Toshifumi Furukawa, Mami Obo, Yumi Yamasaki, Ayako Hotta, Mayuko Kusunoki, Chie Suyama, Naoko Mori, Toshio Honoki, Kanya Fukushima, Nobuyuki J Toxicol Pathol Short Communication To evaluate the involvement of lysophosphatidic acid receptor-1 (LPA1) gene alteration in pancreatic carcinogenesis, we investigated mutations in the LPA1 gene in hamster pancreatic duct adenocarcinomas (PDAs) and established cell lines. Female Syrian golden hamsters received 30 mg/kg of N-nitrosobis(2-oxopropyl)amine (BOP) followed by repeated exposure to an augmentation pressure regimen consisting of a choline-deficient diet combined with DL-ethionine and then L-methionine and a further administration of 20 mg/kg BOP. A total of 10 PDAs obtained 10 weeks after beginning the experiment and three cell lines established from subcutaneously transplantable PDAs in syngeneic hamsters were examined for mutations using reverse transcription-polymerase chain reaction-single strand conformation polymorphism (RT-PCR-SSCP) analysis. A mutation was detected in only one PDA (1/10, 10%) in the form of a GGA to GTA (Gly to Val) transversion at codon 355, and no mutations were detected in the three cell lines. These results suggest that the LPA1 gene mutation may play roles in a limited fraction of BOP-induced pancreatic duct carcinogenesis in hamsters. The Japanese Society of Toxicologic Pathology 2009-04-06 2009-03 /pmc/articles/PMC3246023/ /pubmed/22271981 http://dx.doi.org/10.1293/tox.22.89 Text en ©2009 The Japanese Society of Toxicologic Pathology http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. |
spellingShingle | Short Communication Tsujiuchi, Toshifumi Furukawa, Mami Obo, Yumi Yamasaki, Ayako Hotta, Mayuko Kusunoki, Chie Suyama, Naoko Mori, Toshio Honoki, Kanya Fukushima, Nobuyuki Infrequent Mutation of Lysophosphatidic Acid Receptor-1 Gene in Hamster Pancreatic Duct Adenocarcinomas and Established Cell Lines |
title | Infrequent Mutation of Lysophosphatidic Acid Receptor-1 Gene in Hamster Pancreatic Duct Adenocarcinomas and Established Cell Lines |
title_full | Infrequent Mutation of Lysophosphatidic Acid Receptor-1 Gene in Hamster Pancreatic Duct Adenocarcinomas and Established Cell Lines |
title_fullStr | Infrequent Mutation of Lysophosphatidic Acid Receptor-1 Gene in Hamster Pancreatic Duct Adenocarcinomas and Established Cell Lines |
title_full_unstemmed | Infrequent Mutation of Lysophosphatidic Acid Receptor-1 Gene in Hamster Pancreatic Duct Adenocarcinomas and Established Cell Lines |
title_short | Infrequent Mutation of Lysophosphatidic Acid Receptor-1 Gene in Hamster Pancreatic Duct Adenocarcinomas and Established Cell Lines |
title_sort | infrequent mutation of lysophosphatidic acid receptor-1 gene in hamster pancreatic duct adenocarcinomas and established cell lines |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3246023/ https://www.ncbi.nlm.nih.gov/pubmed/22271981 http://dx.doi.org/10.1293/tox.22.89 |
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