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Preclinical evaluation of sorafenib-eluting stent for suppression of human cholangiocarcinoma cells

BACKGROUND: Cholangiocarcinoma is a malignant tumor arising from the epithelium of the bile ducts. In this study, we prepared sorafenib-loaded biliary stents for potential application as drug-delivery systems for localized treatment of extrahepatic cholangiocarcinoma. METHODS: A sorafenib-coated met...

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Autores principales: Kim, Do Hyung, Jeong, Young-Il, Chung, Chung-Wook, Kim, Cy Hyun, Kwak, Tae Won, Lee, Hye Myeong, Kang, Dae Hwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3646502/
https://www.ncbi.nlm.nih.gov/pubmed/23658488
http://dx.doi.org/10.2147/IJN.S43508
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author Kim, Do Hyung
Jeong, Young-Il
Chung, Chung-Wook
Kim, Cy Hyun
Kwak, Tae Won
Lee, Hye Myeong
Kang, Dae Hwan
author_facet Kim, Do Hyung
Jeong, Young-Il
Chung, Chung-Wook
Kim, Cy Hyun
Kwak, Tae Won
Lee, Hye Myeong
Kang, Dae Hwan
author_sort Kim, Do Hyung
collection PubMed
description BACKGROUND: Cholangiocarcinoma is a malignant tumor arising from the epithelium of the bile ducts. In this study, we prepared sorafenib-loaded biliary stents for potential application as drug-delivery systems for localized treatment of extrahepatic cholangiocarcinoma. METHODS: A sorafenib-coated metal stent was prepared using an electrospray system with the aid of poly(ɛ-caprolactone) (PCL), and then its anticancer activity was investigated using human cholangiocellular carcinoma (HuCC)-T1 cells in vitro and a mouse tumor xenograft model in vivo. Anticancer activity of sorafenib against HuCC-T1 cells was evaluated by the proliferation test, matrix metalloproteinase (MMP) activity, cancer cell invasion, and angiogenesis assay in vitro and in vivo. RESULTS: The drug-release study showed that the increased drug content on the PCL film induced a faster drug-release rate. The growth of cancer cells on the sorafenib-loaded PCL film surfaces decreased in a dose-dependent manner. MMP-2 expression of HuCC-T1 cells gradually decreased according to sorafenib concentration. Furthermore, cancer cell invasion and tube formation of human umbilical vein endothelial cells significantly decreased at sorafenib concentrations higher than 10 mM. In the mouse tumor xenograft model with HuCC-T1 cells, sorafenib-eluting PCL films significantly inhibited the growth of tumor mass and induced apoptosis of tumor cells. Various molecular signals, such as B-cell lymphoma (Bcl)-2, Bcl-2-associated death promoter, Bcl-x, caspase-3, cleaved caspase-3, Fas, signal transducer and activator of transcription 5, extracellular signal-regulated kinases, MMP-9 and pan-janus kinase/stress-activated protein kinase 1, indicated that apoptosis, inhibition of growth and invasion was cleared on sorafenib-eluting PCL films. CONCLUSION: These sorafenib-loaded PCL films are effective in inhibiting angiogenesis, proliferation and invasion of cancer cells. We suggest that sorafenib-loaded PCL film is a promising candidate for the local treatment of cholangiocarcinoma.
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spelling pubmed-36465022013-05-08 Preclinical evaluation of sorafenib-eluting stent for suppression of human cholangiocarcinoma cells Kim, Do Hyung Jeong, Young-Il Chung, Chung-Wook Kim, Cy Hyun Kwak, Tae Won Lee, Hye Myeong Kang, Dae Hwan Int J Nanomedicine Original Research BACKGROUND: Cholangiocarcinoma is a malignant tumor arising from the epithelium of the bile ducts. In this study, we prepared sorafenib-loaded biliary stents for potential application as drug-delivery systems for localized treatment of extrahepatic cholangiocarcinoma. METHODS: A sorafenib-coated metal stent was prepared using an electrospray system with the aid of poly(ɛ-caprolactone) (PCL), and then its anticancer activity was investigated using human cholangiocellular carcinoma (HuCC)-T1 cells in vitro and a mouse tumor xenograft model in vivo. Anticancer activity of sorafenib against HuCC-T1 cells was evaluated by the proliferation test, matrix metalloproteinase (MMP) activity, cancer cell invasion, and angiogenesis assay in vitro and in vivo. RESULTS: The drug-release study showed that the increased drug content on the PCL film induced a faster drug-release rate. The growth of cancer cells on the sorafenib-loaded PCL film surfaces decreased in a dose-dependent manner. MMP-2 expression of HuCC-T1 cells gradually decreased according to sorafenib concentration. Furthermore, cancer cell invasion and tube formation of human umbilical vein endothelial cells significantly decreased at sorafenib concentrations higher than 10 mM. In the mouse tumor xenograft model with HuCC-T1 cells, sorafenib-eluting PCL films significantly inhibited the growth of tumor mass and induced apoptosis of tumor cells. Various molecular signals, such as B-cell lymphoma (Bcl)-2, Bcl-2-associated death promoter, Bcl-x, caspase-3, cleaved caspase-3, Fas, signal transducer and activator of transcription 5, extracellular signal-regulated kinases, MMP-9 and pan-janus kinase/stress-activated protein kinase 1, indicated that apoptosis, inhibition of growth and invasion was cleared on sorafenib-eluting PCL films. CONCLUSION: These sorafenib-loaded PCL films are effective in inhibiting angiogenesis, proliferation and invasion of cancer cells. We suggest that sorafenib-loaded PCL film is a promising candidate for the local treatment of cholangiocarcinoma. Dove Medical Press 2013 2013-04-30 /pmc/articles/PMC3646502/ /pubmed/23658488 http://dx.doi.org/10.2147/IJN.S43508 Text en © 2013 Kim et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Kim, Do Hyung
Jeong, Young-Il
Chung, Chung-Wook
Kim, Cy Hyun
Kwak, Tae Won
Lee, Hye Myeong
Kang, Dae Hwan
Preclinical evaluation of sorafenib-eluting stent for suppression of human cholangiocarcinoma cells
title Preclinical evaluation of sorafenib-eluting stent for suppression of human cholangiocarcinoma cells
title_full Preclinical evaluation of sorafenib-eluting stent for suppression of human cholangiocarcinoma cells
title_fullStr Preclinical evaluation of sorafenib-eluting stent for suppression of human cholangiocarcinoma cells
title_full_unstemmed Preclinical evaluation of sorafenib-eluting stent for suppression of human cholangiocarcinoma cells
title_short Preclinical evaluation of sorafenib-eluting stent for suppression of human cholangiocarcinoma cells
title_sort preclinical evaluation of sorafenib-eluting stent for suppression of human cholangiocarcinoma cells
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3646502/
https://www.ncbi.nlm.nih.gov/pubmed/23658488
http://dx.doi.org/10.2147/IJN.S43508
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