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Metformin potentiates anti-tumor effect of resveratrol on pancreatic cancer by down-regulation of VEGF-B signaling pathway

Our previous study showed that resveratrol (RSV) exhibited not only anti-tumor effect, but also had potential tumor promotion effect on pancreatic cancer (Paca) cells through up-regulation of VEGF-B. We determined whether metformin (MET) could potentiate the anti-tumor effect of RSV on PaCa in this...

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Autores principales: Zhu, Mengmeng, Zhang, Qiong, Wang, Xiaoling, Kang, Licheng, Yang, Yinan, Liu, Yuansheng, Yang, Lei, Li, Jing, Yang, Liang, Liu, Jie, Li, Yin, Zu, Lingling, Shen, Yanna, Qi, Zhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356654/
https://www.ncbi.nlm.nih.gov/pubmed/27705937
http://dx.doi.org/10.18632/oncotarget.12391
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author Zhu, Mengmeng
Zhang, Qiong
Wang, Xiaoling
Kang, Licheng
Yang, Yinan
Liu, Yuansheng
Yang, Lei
Li, Jing
Yang, Liang
Liu, Jie
Li, Yin
Zu, Lingling
Shen, Yanna
Qi, Zhi
author_facet Zhu, Mengmeng
Zhang, Qiong
Wang, Xiaoling
Kang, Licheng
Yang, Yinan
Liu, Yuansheng
Yang, Lei
Li, Jing
Yang, Liang
Liu, Jie
Li, Yin
Zu, Lingling
Shen, Yanna
Qi, Zhi
author_sort Zhu, Mengmeng
collection PubMed
description Our previous study showed that resveratrol (RSV) exhibited not only anti-tumor effect, but also had potential tumor promotion effect on pancreatic cancer (Paca) cells through up-regulation of VEGF-B. We determined whether metformin (MET) could potentiate the anti-tumor effect of RSV on PaCa in this study. Combination of RSV (100 μmol/l) and MET (20 mmol/l) significantly inhibited tumor growth and increased apoptosis of human PaCa in comparison with RSV or MET alone treatment in PaCa cell lines (Miapaca-2, Panc-1 and Capan-2). Combination of RSV (60 mg/kg, gavage) and MET (250 mg/kg, i.p.) significantly inhibited tumor growth in PaCa bearing nude mice (subcutaneous injection of 5 × 10(6) Miapaca-2 cells) in comparison with RSV or MET alone treatment on day 40. Combination treatment significantly decreased VEGF-B expression and inhibited activity of GSK-3β when compared to the RSV alone treatment. Up-regulated expressions of Bax, cleaved caspase-3 and down-regulated expression of Bcl-2 were observed in RSV+ MET group in comparison with RSV group either in vitro or in vivo. Inhibition of VEGF-B by VEGF-B small interfering RNA (siRNA) mimicked the effects of MET on PaCa cells. These results suggested that MET, a potential pharmacological inhibitor of VEGF-B signaling pathway, potentiated the anti-tumor effect of RSV on PaCa, and combination of MET and RSV would be a promising modality for clinical PaCa therapy.
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spelling pubmed-53566542017-04-26 Metformin potentiates anti-tumor effect of resveratrol on pancreatic cancer by down-regulation of VEGF-B signaling pathway Zhu, Mengmeng Zhang, Qiong Wang, Xiaoling Kang, Licheng Yang, Yinan Liu, Yuansheng Yang, Lei Li, Jing Yang, Liang Liu, Jie Li, Yin Zu, Lingling Shen, Yanna Qi, Zhi Oncotarget Research Paper Our previous study showed that resveratrol (RSV) exhibited not only anti-tumor effect, but also had potential tumor promotion effect on pancreatic cancer (Paca) cells through up-regulation of VEGF-B. We determined whether metformin (MET) could potentiate the anti-tumor effect of RSV on PaCa in this study. Combination of RSV (100 μmol/l) and MET (20 mmol/l) significantly inhibited tumor growth and increased apoptosis of human PaCa in comparison with RSV or MET alone treatment in PaCa cell lines (Miapaca-2, Panc-1 and Capan-2). Combination of RSV (60 mg/kg, gavage) and MET (250 mg/kg, i.p.) significantly inhibited tumor growth in PaCa bearing nude mice (subcutaneous injection of 5 × 10(6) Miapaca-2 cells) in comparison with RSV or MET alone treatment on day 40. Combination treatment significantly decreased VEGF-B expression and inhibited activity of GSK-3β when compared to the RSV alone treatment. Up-regulated expressions of Bax, cleaved caspase-3 and down-regulated expression of Bcl-2 were observed in RSV+ MET group in comparison with RSV group either in vitro or in vivo. Inhibition of VEGF-B by VEGF-B small interfering RNA (siRNA) mimicked the effects of MET on PaCa cells. These results suggested that MET, a potential pharmacological inhibitor of VEGF-B signaling pathway, potentiated the anti-tumor effect of RSV on PaCa, and combination of MET and RSV would be a promising modality for clinical PaCa therapy. Impact Journals LLC 2016-10-01 /pmc/articles/PMC5356654/ /pubmed/27705937 http://dx.doi.org/10.18632/oncotarget.12391 Text en Copyright: © 2016 Zhu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Zhu, Mengmeng
Zhang, Qiong
Wang, Xiaoling
Kang, Licheng
Yang, Yinan
Liu, Yuansheng
Yang, Lei
Li, Jing
Yang, Liang
Liu, Jie
Li, Yin
Zu, Lingling
Shen, Yanna
Qi, Zhi
Metformin potentiates anti-tumor effect of resveratrol on pancreatic cancer by down-regulation of VEGF-B signaling pathway
title Metformin potentiates anti-tumor effect of resveratrol on pancreatic cancer by down-regulation of VEGF-B signaling pathway
title_full Metformin potentiates anti-tumor effect of resveratrol on pancreatic cancer by down-regulation of VEGF-B signaling pathway
title_fullStr Metformin potentiates anti-tumor effect of resveratrol on pancreatic cancer by down-regulation of VEGF-B signaling pathway
title_full_unstemmed Metformin potentiates anti-tumor effect of resveratrol on pancreatic cancer by down-regulation of VEGF-B signaling pathway
title_short Metformin potentiates anti-tumor effect of resveratrol on pancreatic cancer by down-regulation of VEGF-B signaling pathway
title_sort metformin potentiates anti-tumor effect of resveratrol on pancreatic cancer by down-regulation of vegf-b signaling pathway
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356654/
https://www.ncbi.nlm.nih.gov/pubmed/27705937
http://dx.doi.org/10.18632/oncotarget.12391
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