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Synergistic anti-tumor effects of liraglutide with metformin on pancreatic cancer cells
Either metformin or liraglutide has been reported to have anti-tumor effects on pancreatic cancer cells. However, it is not clear whether their combined treatment has additive or synergistic anti-tumor effects on pancreatic cancer cells. In this study, the human pancreatic cancer cell line MiaPaca-2...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999272/ https://www.ncbi.nlm.nih.gov/pubmed/29897998 http://dx.doi.org/10.1371/journal.pone.0198938 |
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author | Lu, Ran Yang, Jin Wei, Rui Ke, Jing Tian, Qing Yu, Fei Liu, Junling Zhang, Jingjing Hong, Tianpei |
author_facet | Lu, Ran Yang, Jin Wei, Rui Ke, Jing Tian, Qing Yu, Fei Liu, Junling Zhang, Jingjing Hong, Tianpei |
author_sort | Lu, Ran |
collection | PubMed |
description | Either metformin or liraglutide has been reported to have anti-tumor effects on pancreatic cancer cells. However, it is not clear whether their combined treatment has additive or synergistic anti-tumor effects on pancreatic cancer cells. In this study, the human pancreatic cancer cell line MiaPaca-2 was incubated with liraglutide and/or metformin. The cell Counting Kit-8 (CCK-8), colony formation, flow cytometry, and wound-healing and transwell migration assays were used to detect cell viability, clonogenic survival, cell cycle and cell migration, respectively. RT-PCR and western blot analyses were used to determine the mRNA and protein levels of related molecules. Results showed that combination treatment with liraglutide (100 nmol/L) and metformin (0.75 mmol/L) significantly decreased cell viability and colony formation, caused cell cycle arrest, upregulated the level of pro-apoptotic proteins Bax and cleaved caspase-3, and inhibited cell migration in the cells, although their single treatment did not exhibit such effects. Combination index value for cell viability indicated a synergistic interaction of liraglutide and metformin. Moreover, the combined treatment with liraglutide and metformin could activate the phosphorylation of AMP-activated protein kinase (AMPK) more potently than their single treatment in the cells. These results suggest that liraglutide in combination with metformin has a synergistic anti-tumor effect on the pancreatic cancer cells, which may be at least partly due to activation of AMPK signaling. Our study provides new insights into the treatment of patients with type 2 diabetes and pancreatic cancer. |
format | Online Article Text |
id | pubmed-5999272 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-59992722018-06-21 Synergistic anti-tumor effects of liraglutide with metformin on pancreatic cancer cells Lu, Ran Yang, Jin Wei, Rui Ke, Jing Tian, Qing Yu, Fei Liu, Junling Zhang, Jingjing Hong, Tianpei PLoS One Research Article Either metformin or liraglutide has been reported to have anti-tumor effects on pancreatic cancer cells. However, it is not clear whether their combined treatment has additive or synergistic anti-tumor effects on pancreatic cancer cells. In this study, the human pancreatic cancer cell line MiaPaca-2 was incubated with liraglutide and/or metformin. The cell Counting Kit-8 (CCK-8), colony formation, flow cytometry, and wound-healing and transwell migration assays were used to detect cell viability, clonogenic survival, cell cycle and cell migration, respectively. RT-PCR and western blot analyses were used to determine the mRNA and protein levels of related molecules. Results showed that combination treatment with liraglutide (100 nmol/L) and metformin (0.75 mmol/L) significantly decreased cell viability and colony formation, caused cell cycle arrest, upregulated the level of pro-apoptotic proteins Bax and cleaved caspase-3, and inhibited cell migration in the cells, although their single treatment did not exhibit such effects. Combination index value for cell viability indicated a synergistic interaction of liraglutide and metformin. Moreover, the combined treatment with liraglutide and metformin could activate the phosphorylation of AMP-activated protein kinase (AMPK) more potently than their single treatment in the cells. These results suggest that liraglutide in combination with metformin has a synergistic anti-tumor effect on the pancreatic cancer cells, which may be at least partly due to activation of AMPK signaling. Our study provides new insights into the treatment of patients with type 2 diabetes and pancreatic cancer. Public Library of Science 2018-06-13 /pmc/articles/PMC5999272/ /pubmed/29897998 http://dx.doi.org/10.1371/journal.pone.0198938 Text en © 2018 Lu et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Lu, Ran Yang, Jin Wei, Rui Ke, Jing Tian, Qing Yu, Fei Liu, Junling Zhang, Jingjing Hong, Tianpei Synergistic anti-tumor effects of liraglutide with metformin on pancreatic cancer cells |
title | Synergistic anti-tumor effects of liraglutide with metformin on pancreatic cancer cells |
title_full | Synergistic anti-tumor effects of liraglutide with metformin on pancreatic cancer cells |
title_fullStr | Synergistic anti-tumor effects of liraglutide with metformin on pancreatic cancer cells |
title_full_unstemmed | Synergistic anti-tumor effects of liraglutide with metformin on pancreatic cancer cells |
title_short | Synergistic anti-tumor effects of liraglutide with metformin on pancreatic cancer cells |
title_sort | synergistic anti-tumor effects of liraglutide with metformin on pancreatic cancer cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999272/ https://www.ncbi.nlm.nih.gov/pubmed/29897998 http://dx.doi.org/10.1371/journal.pone.0198938 |
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