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Argininosuccinate synthetase 1 suppression and arginine restriction inhibit cell migration in gastric cancer cell lines
Gastric cancer metastasis remains a major cause of cancer-related deaths. There is an urgent need to develop new therapeutic approaches targeting metastatic gastric cancer. Argininosuccinate synthetase 1 (ASS1) expression is increased in gastric cancer. We detected the protein expression of ASS1 in...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415574/ https://www.ncbi.nlm.nih.gov/pubmed/25928182 http://dx.doi.org/10.1038/srep09783 |
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author | Shan, Yan-Shen Hsu, Hui-Ping Lai, Ming-Derg Yen, Meng-Chi Chen, Wei-Ching Fang, Jung-Hua Weng, Tzu-Yang Chen, Yi-Ling |
author_facet | Shan, Yan-Shen Hsu, Hui-Ping Lai, Ming-Derg Yen, Meng-Chi Chen, Wei-Ching Fang, Jung-Hua Weng, Tzu-Yang Chen, Yi-Ling |
author_sort | Shan, Yan-Shen |
collection | PubMed |
description | Gastric cancer metastasis remains a major cause of cancer-related deaths. There is an urgent need to develop new therapeutic approaches targeting metastatic gastric cancer. Argininosuccinate synthetase 1 (ASS1) expression is increased in gastric cancer. We detected the protein expression of ASS1 in human gastric cancer cell lines (AGS, NCI-N87, and MKN45) and in murine gastric cancer cell lines (3I and 3IB2). We used vector-mediated short hairpin RNA (shRNA) expression to silence ASS1 expression in the MKN45 and 3IB2 cell lines, and analyzed the effects of this protein on cell migration and metastasis. We demonstrated that ASS1 silencing suppressed cell migration in the MKN45 and 3IB2 cell lines. ASS1 knockdown significantly reduced liver metastasis in mice after the intrasplenic implantation of 3IB2 cancer cell clones. To determine whether arginine restriction may represent a therapeutic approach to treat gastric cancer, the sensitivity of tumor cells to arginine depletion was determined in gastric cancer cells. Arginine depletion significantly inhibited cell migration in the gastric cancer cell line. The silencing of ASS1 expression in MKN45 and 3IB2 gastric cancer cells markedly decreased STAT3 protein expression. In conclusion, our results indicate that the ASS1 protein is required for cell migration in gastric cancer cell lines. |
format | Online Article Text |
id | pubmed-4415574 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-44155742015-05-08 Argininosuccinate synthetase 1 suppression and arginine restriction inhibit cell migration in gastric cancer cell lines Shan, Yan-Shen Hsu, Hui-Ping Lai, Ming-Derg Yen, Meng-Chi Chen, Wei-Ching Fang, Jung-Hua Weng, Tzu-Yang Chen, Yi-Ling Sci Rep Article Gastric cancer metastasis remains a major cause of cancer-related deaths. There is an urgent need to develop new therapeutic approaches targeting metastatic gastric cancer. Argininosuccinate synthetase 1 (ASS1) expression is increased in gastric cancer. We detected the protein expression of ASS1 in human gastric cancer cell lines (AGS, NCI-N87, and MKN45) and in murine gastric cancer cell lines (3I and 3IB2). We used vector-mediated short hairpin RNA (shRNA) expression to silence ASS1 expression in the MKN45 and 3IB2 cell lines, and analyzed the effects of this protein on cell migration and metastasis. We demonstrated that ASS1 silencing suppressed cell migration in the MKN45 and 3IB2 cell lines. ASS1 knockdown significantly reduced liver metastasis in mice after the intrasplenic implantation of 3IB2 cancer cell clones. To determine whether arginine restriction may represent a therapeutic approach to treat gastric cancer, the sensitivity of tumor cells to arginine depletion was determined in gastric cancer cells. Arginine depletion significantly inhibited cell migration in the gastric cancer cell line. The silencing of ASS1 expression in MKN45 and 3IB2 gastric cancer cells markedly decreased STAT3 protein expression. In conclusion, our results indicate that the ASS1 protein is required for cell migration in gastric cancer cell lines. Nature Publishing Group 2015-04-30 /pmc/articles/PMC4415574/ /pubmed/25928182 http://dx.doi.org/10.1038/srep09783 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Shan, Yan-Shen Hsu, Hui-Ping Lai, Ming-Derg Yen, Meng-Chi Chen, Wei-Ching Fang, Jung-Hua Weng, Tzu-Yang Chen, Yi-Ling Argininosuccinate synthetase 1 suppression and arginine restriction inhibit cell migration in gastric cancer cell lines |
title | Argininosuccinate synthetase 1 suppression and arginine restriction inhibit cell
migration in gastric cancer cell lines |
title_full | Argininosuccinate synthetase 1 suppression and arginine restriction inhibit cell
migration in gastric cancer cell lines |
title_fullStr | Argininosuccinate synthetase 1 suppression and arginine restriction inhibit cell
migration in gastric cancer cell lines |
title_full_unstemmed | Argininosuccinate synthetase 1 suppression and arginine restriction inhibit cell
migration in gastric cancer cell lines |
title_short | Argininosuccinate synthetase 1 suppression and arginine restriction inhibit cell
migration in gastric cancer cell lines |
title_sort | argininosuccinate synthetase 1 suppression and arginine restriction inhibit cell
migration in gastric cancer cell lines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415574/ https://www.ncbi.nlm.nih.gov/pubmed/25928182 http://dx.doi.org/10.1038/srep09783 |
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