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Metformin suppressed the proliferation of LoVo cells and induced a time-dependent metabolic and transcriptional alteration
Metformin is a widely used anti-diabetic drug with potential anti-tumor activity. However, little is known about its global metabolic and transcriptional impacts on tumor cells. In current study, we performed a metabolic profiling on human-derived colon cancer LoVo cells treated by 10 mM metformin f...
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/PMC4663508/ https://www.ncbi.nlm.nih.gov/pubmed/26616174 http://dx.doi.org/10.1038/srep17423 |
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author | He, Jiaojiao Wang, Ke Zheng, Ningning Qiu, Yunping Xie, Guoxiang Su, Mingming Jia, Wei Li, Houkai |
author_facet | He, Jiaojiao Wang, Ke Zheng, Ningning Qiu, Yunping Xie, Guoxiang Su, Mingming Jia, Wei Li, Houkai |
author_sort | He, Jiaojiao |
collection | PubMed |
description | Metformin is a widely used anti-diabetic drug with potential anti-tumor activity. However, little is known about its global metabolic and transcriptional impacts on tumor cells. In current study, we performed a metabolic profiling on human-derived colon cancer LoVo cells treated by 10 mM metformin for 8, 24 and 48 h. An obvious time-dependent metabolic alteration was observed from 8 to 48 h, prior to the reduction of cell viability. A total of 47, 45 and 66 differential metabolites were identified between control and metformin-treated cells at three time points. Most of the metabolites were up-regulated at 8 h, but down-regulated at 24 and 48 h by metformin. These metabolites were mainly involved in carbohydrates, lipids, amino acids, vitamins and nucleotides metabolism pathways. Meanwhile, the transcirptomic profile revealed 134 and 3061 differentially expressed genes at 8 and 24 h by metformin. In addition to the cancer signaling pathways, expression of genes involved in cell energy metabolism pathways was significantly altered, which were further validated with genes in glucose metabolism pathway. Altogether, our current data indicate that metformin suppressed the proliferation of LoVo cells, which may be due to the modulation on cell energy metabolism at both metabolic and transcriptional levels in a time-dependent way. |
format | Online Article Text |
id | pubmed-4663508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46635082015-12-03 Metformin suppressed the proliferation of LoVo cells and induced a time-dependent metabolic and transcriptional alteration He, Jiaojiao Wang, Ke Zheng, Ningning Qiu, Yunping Xie, Guoxiang Su, Mingming Jia, Wei Li, Houkai Sci Rep Article Metformin is a widely used anti-diabetic drug with potential anti-tumor activity. However, little is known about its global metabolic and transcriptional impacts on tumor cells. In current study, we performed a metabolic profiling on human-derived colon cancer LoVo cells treated by 10 mM metformin for 8, 24 and 48 h. An obvious time-dependent metabolic alteration was observed from 8 to 48 h, prior to the reduction of cell viability. A total of 47, 45 and 66 differential metabolites were identified between control and metformin-treated cells at three time points. Most of the metabolites were up-regulated at 8 h, but down-regulated at 24 and 48 h by metformin. These metabolites were mainly involved in carbohydrates, lipids, amino acids, vitamins and nucleotides metabolism pathways. Meanwhile, the transcirptomic profile revealed 134 and 3061 differentially expressed genes at 8 and 24 h by metformin. In addition to the cancer signaling pathways, expression of genes involved in cell energy metabolism pathways was significantly altered, which were further validated with genes in glucose metabolism pathway. Altogether, our current data indicate that metformin suppressed the proliferation of LoVo cells, which may be due to the modulation on cell energy metabolism at both metabolic and transcriptional levels in a time-dependent way. Nature Publishing Group 2015-11-30 /pmc/articles/PMC4663508/ /pubmed/26616174 http://dx.doi.org/10.1038/srep17423 Text en Copyright © 2015, Macmillan Publishers Limited 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 to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article He, Jiaojiao Wang, Ke Zheng, Ningning Qiu, Yunping Xie, Guoxiang Su, Mingming Jia, Wei Li, Houkai Metformin suppressed the proliferation of LoVo cells and induced a time-dependent metabolic and transcriptional alteration |
title | Metformin suppressed the proliferation of LoVo cells and induced a time-dependent metabolic and transcriptional alteration |
title_full | Metformin suppressed the proliferation of LoVo cells and induced a time-dependent metabolic and transcriptional alteration |
title_fullStr | Metformin suppressed the proliferation of LoVo cells and induced a time-dependent metabolic and transcriptional alteration |
title_full_unstemmed | Metformin suppressed the proliferation of LoVo cells and induced a time-dependent metabolic and transcriptional alteration |
title_short | Metformin suppressed the proliferation of LoVo cells and induced a time-dependent metabolic and transcriptional alteration |
title_sort | metformin suppressed the proliferation of lovo cells and induced a time-dependent metabolic and transcriptional alteration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4663508/ https://www.ncbi.nlm.nih.gov/pubmed/26616174 http://dx.doi.org/10.1038/srep17423 |
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