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TPGS-1000 exhibits potent anticancer activity for hepatocellular carcinoma in vitro and in vivo

D-alpha-tocopheryl polyethylene glycol 1000 succinate (TPGS1000) is the most active water-soluble derivative of vitamin E and has been widely used as a carrier of solvents, plasticizers, emulsifiers, absorbent agents and refractory drug delivery systems. However, its anti-hepatocellular carcinoma (H...

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Autores principales: Chen, Yidan, Mo, Liqin, Wang, Xuan, Chen, Bi, Hua, Yunfen, Gong, Linyan, Yang, Fei, Li, Yongqiang, Chen, Fangfang, Zhu, Guiting, Ni, Wei, Zhang, Cheng, Cheng, Yuming, Luo, Yan, Shi, Junping, Qiu, Mengsheng, Wu, Shixiu, Tan, Zhou, Wang, Kaifeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7053644/
https://www.ncbi.nlm.nih.gov/pubmed/31986488
http://dx.doi.org/10.18632/aging.102704
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author Chen, Yidan
Mo, Liqin
Wang, Xuan
Chen, Bi
Hua, Yunfen
Gong, Linyan
Yang, Fei
Li, Yongqiang
Chen, Fangfang
Zhu, Guiting
Ni, Wei
Zhang, Cheng
Cheng, Yuming
Luo, Yan
Shi, Junping
Qiu, Mengsheng
Wu, Shixiu
Tan, Zhou
Wang, Kaifeng
author_facet Chen, Yidan
Mo, Liqin
Wang, Xuan
Chen, Bi
Hua, Yunfen
Gong, Linyan
Yang, Fei
Li, Yongqiang
Chen, Fangfang
Zhu, Guiting
Ni, Wei
Zhang, Cheng
Cheng, Yuming
Luo, Yan
Shi, Junping
Qiu, Mengsheng
Wu, Shixiu
Tan, Zhou
Wang, Kaifeng
author_sort Chen, Yidan
collection PubMed
description D-alpha-tocopheryl polyethylene glycol 1000 succinate (TPGS1000) is the most active water-soluble derivative of vitamin E and has been widely used as a carrier of solvents, plasticizers, emulsifiers, absorbent agents and refractory drug delivery systems. However, its anti-hepatocellular carcinoma (HCC) properties have not been explored. HCC cells were treated with different concentrations of TPGS1000. Cell survival was tested by CCK8 assay, and cell migration was tested by wound healing and Transwell assay. EdU staining verified cell proliferation, and signalling pathway was assayed by Western blot analysis. The BALB/c-nu mouse xenograft model was established to test HCC cell growth in vivo. In vitro TPGS1000 significantly inhibited the viability and mobility of HCC cells (HepG2, Hep3B and Huh7) in a dose-dependent manner. Cell cycle analysis indicated that TPGS1000 treatment arrested the HCC cell cycle in the G0/G1 phase, and induction of cell apoptosis was confirmed by TUNEL and Annexin V-7-AAD staining. Further pharmacological analysis indicated that collapse of the transmembrane potential of mitochondria, increased ROS generation, PARP-induced cell apoptosis and FoxM1-p21-mediated cell cycle arresting, were involved in the anti-HCC activity of TPGS1000. Moreover, treatment in vivo with TPGS1000 effectively impaired the growth of HCC xenografts in nude mice.
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spelling pubmed-70536442020-03-12 TPGS-1000 exhibits potent anticancer activity for hepatocellular carcinoma in vitro and in vivo Chen, Yidan Mo, Liqin Wang, Xuan Chen, Bi Hua, Yunfen Gong, Linyan Yang, Fei Li, Yongqiang Chen, Fangfang Zhu, Guiting Ni, Wei Zhang, Cheng Cheng, Yuming Luo, Yan Shi, Junping Qiu, Mengsheng Wu, Shixiu Tan, Zhou Wang, Kaifeng Aging (Albany NY) Research Paper D-alpha-tocopheryl polyethylene glycol 1000 succinate (TPGS1000) is the most active water-soluble derivative of vitamin E and has been widely used as a carrier of solvents, plasticizers, emulsifiers, absorbent agents and refractory drug delivery systems. However, its anti-hepatocellular carcinoma (HCC) properties have not been explored. HCC cells were treated with different concentrations of TPGS1000. Cell survival was tested by CCK8 assay, and cell migration was tested by wound healing and Transwell assay. EdU staining verified cell proliferation, and signalling pathway was assayed by Western blot analysis. The BALB/c-nu mouse xenograft model was established to test HCC cell growth in vivo. In vitro TPGS1000 significantly inhibited the viability and mobility of HCC cells (HepG2, Hep3B and Huh7) in a dose-dependent manner. Cell cycle analysis indicated that TPGS1000 treatment arrested the HCC cell cycle in the G0/G1 phase, and induction of cell apoptosis was confirmed by TUNEL and Annexin V-7-AAD staining. Further pharmacological analysis indicated that collapse of the transmembrane potential of mitochondria, increased ROS generation, PARP-induced cell apoptosis and FoxM1-p21-mediated cell cycle arresting, were involved in the anti-HCC activity of TPGS1000. Moreover, treatment in vivo with TPGS1000 effectively impaired the growth of HCC xenografts in nude mice. Impact Journals 2020-01-27 /pmc/articles/PMC7053644/ /pubmed/31986488 http://dx.doi.org/10.18632/aging.102704 Text en Copyright © 2020 Chen 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 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Chen, Yidan
Mo, Liqin
Wang, Xuan
Chen, Bi
Hua, Yunfen
Gong, Linyan
Yang, Fei
Li, Yongqiang
Chen, Fangfang
Zhu, Guiting
Ni, Wei
Zhang, Cheng
Cheng, Yuming
Luo, Yan
Shi, Junping
Qiu, Mengsheng
Wu, Shixiu
Tan, Zhou
Wang, Kaifeng
TPGS-1000 exhibits potent anticancer activity for hepatocellular carcinoma in vitro and in vivo
title TPGS-1000 exhibits potent anticancer activity for hepatocellular carcinoma in vitro and in vivo
title_full TPGS-1000 exhibits potent anticancer activity for hepatocellular carcinoma in vitro and in vivo
title_fullStr TPGS-1000 exhibits potent anticancer activity for hepatocellular carcinoma in vitro and in vivo
title_full_unstemmed TPGS-1000 exhibits potent anticancer activity for hepatocellular carcinoma in vitro and in vivo
title_short TPGS-1000 exhibits potent anticancer activity for hepatocellular carcinoma in vitro and in vivo
title_sort tpgs-1000 exhibits potent anticancer activity for hepatocellular carcinoma in vitro and in vivo
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7053644/
https://www.ncbi.nlm.nih.gov/pubmed/31986488
http://dx.doi.org/10.18632/aging.102704
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