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Metabolic characterization of invaded cells of the pancreatic cancer cell line, PANC‐1
We previously reported that about 0.4% of cells in the cultured human pancreatic cancer cell line, PANC‐1, can invade matrigel during the transwell invasion assay, suggesting that these invaded PANC‐1 cells may have specific characteristics to keep their invasive potential. To identify the metabolic...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5448609/ https://www.ncbi.nlm.nih.gov/pubmed/28256041 http://dx.doi.org/10.1111/cas.13220 |
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author | Fujita, Mayumi Imadome, Kaori Imai, Takashi |
author_facet | Fujita, Mayumi Imadome, Kaori Imai, Takashi |
author_sort | Fujita, Mayumi |
collection | PubMed |
description | We previously reported that about 0.4% of cells in the cultured human pancreatic cancer cell line, PANC‐1, can invade matrigel during the transwell invasion assay, suggesting that these invaded PANC‐1 cells may have specific characteristics to keep their invasive potential. To identify the metabolic characterization specific in the invaded PANC‐1 cells, metabolome analysis of the invaded PANC‐1 compared with the whole cultured PANC‐1 was performed using CE‐TOFMS, and concentrations of 110 metabolites were measured. In contrast to the whole cultured cells, the invaded PANC‐1 was characterized as a population with reduced levels of amino acids and TCA cycle intermediates, and decreased and increased intermediates in glycolysis and nucleic acid metabolism. In particular, the ratio of both adenosine and guanosine energy charge was reduced in the invaded cells, revealing that the consumption of ATP and GTP was high in the invaded cells, and thus suggesting that ATP‐ or GTP‐generating pathways are stimulated. In addition, the GSH/GSSG ratio was low in the invaded cells, but these cells had a higher surviving fraction after exposure to hydrogen peroxide. Thus, the invaded cells were the population resistant to oxidative stress. Furthermore, reduction in intracellular GSH content inhibited PANC‐1 invasiveness, indicated that GSH has an important role in PANC‐1 invasiveness. Overall, we propose the invaded cells have several unique metabolic profiles. |
format | Online Article Text |
id | pubmed-5448609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54486092017-06-01 Metabolic characterization of invaded cells of the pancreatic cancer cell line, PANC‐1 Fujita, Mayumi Imadome, Kaori Imai, Takashi Cancer Sci Original Articles We previously reported that about 0.4% of cells in the cultured human pancreatic cancer cell line, PANC‐1, can invade matrigel during the transwell invasion assay, suggesting that these invaded PANC‐1 cells may have specific characteristics to keep their invasive potential. To identify the metabolic characterization specific in the invaded PANC‐1 cells, metabolome analysis of the invaded PANC‐1 compared with the whole cultured PANC‐1 was performed using CE‐TOFMS, and concentrations of 110 metabolites were measured. In contrast to the whole cultured cells, the invaded PANC‐1 was characterized as a population with reduced levels of amino acids and TCA cycle intermediates, and decreased and increased intermediates in glycolysis and nucleic acid metabolism. In particular, the ratio of both adenosine and guanosine energy charge was reduced in the invaded cells, revealing that the consumption of ATP and GTP was high in the invaded cells, and thus suggesting that ATP‐ or GTP‐generating pathways are stimulated. In addition, the GSH/GSSG ratio was low in the invaded cells, but these cells had a higher surviving fraction after exposure to hydrogen peroxide. Thus, the invaded cells were the population resistant to oxidative stress. Furthermore, reduction in intracellular GSH content inhibited PANC‐1 invasiveness, indicated that GSH has an important role in PANC‐1 invasiveness. Overall, we propose the invaded cells have several unique metabolic profiles. John Wiley and Sons Inc. 2017-05-05 2017-05 /pmc/articles/PMC5448609/ /pubmed/28256041 http://dx.doi.org/10.1111/cas.13220 Text en © 2017 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Fujita, Mayumi Imadome, Kaori Imai, Takashi Metabolic characterization of invaded cells of the pancreatic cancer cell line, PANC‐1 |
title | Metabolic characterization of invaded cells of the pancreatic cancer cell line, PANC‐1 |
title_full | Metabolic characterization of invaded cells of the pancreatic cancer cell line, PANC‐1 |
title_fullStr | Metabolic characterization of invaded cells of the pancreatic cancer cell line, PANC‐1 |
title_full_unstemmed | Metabolic characterization of invaded cells of the pancreatic cancer cell line, PANC‐1 |
title_short | Metabolic characterization of invaded cells of the pancreatic cancer cell line, PANC‐1 |
title_sort | metabolic characterization of invaded cells of the pancreatic cancer cell line, panc‐1 |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5448609/ https://www.ncbi.nlm.nih.gov/pubmed/28256041 http://dx.doi.org/10.1111/cas.13220 |
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