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Anticancer activity of streptochlorin, a novel antineoplastic agent, in cholangiocarcinoma
BACKGROUND: The aim of this study is to investigate the anticancer activity of streptochlorin, a novel antineoplastic agent, in cholangiocarcinoma. METHODS: The anticancer activity of streptochlorin was evaluated in vitro in various cholangiocarcinoma cell lines for apoptosis, proliferation, invasiv...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4404940/ https://www.ncbi.nlm.nih.gov/pubmed/25931814 http://dx.doi.org/10.2147/DDDT.S80205 |
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author | Kwak, Tae Won Shin, Hee Jae Jeong, Young-Il Han, Myoung-Eun Oh, Sae-Ock Kim, Hyun-Jung Kim, Do Hyung Kang, Dae Hwan |
author_facet | Kwak, Tae Won Shin, Hee Jae Jeong, Young-Il Han, Myoung-Eun Oh, Sae-Ock Kim, Hyun-Jung Kim, Do Hyung Kang, Dae Hwan |
author_sort | Kwak, Tae Won |
collection | PubMed |
description | BACKGROUND: The aim of this study is to investigate the anticancer activity of streptochlorin, a novel antineoplastic agent, in cholangiocarcinoma. METHODS: The anticancer activity of streptochlorin was evaluated in vitro in various cholangiocarcinoma cell lines for apoptosis, proliferation, invasiveness, and expression of various protein levels. A liver metastasis model was prepared by splenic injection of HuCC-T1 cholangiocarcinoma cells using a BALB/c nude mouse model to study the systemic antimetastatic efficacy of streptochlorin 5 mg/kg at 8 weeks. The antitumor efficacy of subcutaneously injected streptochlorin was also assessed using a solid tumor xenograft model of SNU478 cells for 22 days in the BALB/c nude mouse. RESULTS: Streptochlorin inhibited growth and secretion of vascular endothelial growth factor by cholangiocarcinoma cells in a dose-dependent manner and induced apoptosis in vitro. In addition, streptochlorin effectively inhibited invasion and migration of cholangiocarcinoma cells. Secretion of vascular endothelial growth factor and activity of matrix metalloproteinase-9 in cholangiocarcinoma cells were also suppressed by treatment with streptochlorin. Streptochlorin effectively regulated metastasis of HuCC-T1 cells in a mouse model of liver metastasis. In a tumor xenograft study using SNU478 cells, streptochlorin significantly inhibited tumor growth without changes in body weight when compared with the control. CONCLUSION: These results reveal that streptochlorin is a promising chemotherapeutic agent to the treatment of cholangiocarcinoma. |
format | Online Article Text |
id | pubmed-4404940 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44049402015-04-30 Anticancer activity of streptochlorin, a novel antineoplastic agent, in cholangiocarcinoma Kwak, Tae Won Shin, Hee Jae Jeong, Young-Il Han, Myoung-Eun Oh, Sae-Ock Kim, Hyun-Jung Kim, Do Hyung Kang, Dae Hwan Drug Des Devel Ther Original Research BACKGROUND: The aim of this study is to investigate the anticancer activity of streptochlorin, a novel antineoplastic agent, in cholangiocarcinoma. METHODS: The anticancer activity of streptochlorin was evaluated in vitro in various cholangiocarcinoma cell lines for apoptosis, proliferation, invasiveness, and expression of various protein levels. A liver metastasis model was prepared by splenic injection of HuCC-T1 cholangiocarcinoma cells using a BALB/c nude mouse model to study the systemic antimetastatic efficacy of streptochlorin 5 mg/kg at 8 weeks. The antitumor efficacy of subcutaneously injected streptochlorin was also assessed using a solid tumor xenograft model of SNU478 cells for 22 days in the BALB/c nude mouse. RESULTS: Streptochlorin inhibited growth and secretion of vascular endothelial growth factor by cholangiocarcinoma cells in a dose-dependent manner and induced apoptosis in vitro. In addition, streptochlorin effectively inhibited invasion and migration of cholangiocarcinoma cells. Secretion of vascular endothelial growth factor and activity of matrix metalloproteinase-9 in cholangiocarcinoma cells were also suppressed by treatment with streptochlorin. Streptochlorin effectively regulated metastasis of HuCC-T1 cells in a mouse model of liver metastasis. In a tumor xenograft study using SNU478 cells, streptochlorin significantly inhibited tumor growth without changes in body weight when compared with the control. CONCLUSION: These results reveal that streptochlorin is a promising chemotherapeutic agent to the treatment of cholangiocarcinoma. Dove Medical Press 2015-04-16 /pmc/articles/PMC4404940/ /pubmed/25931814 http://dx.doi.org/10.2147/DDDT.S80205 Text en © 2015 Kwak et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Kwak, Tae Won Shin, Hee Jae Jeong, Young-Il Han, Myoung-Eun Oh, Sae-Ock Kim, Hyun-Jung Kim, Do Hyung Kang, Dae Hwan Anticancer activity of streptochlorin, a novel antineoplastic agent, in cholangiocarcinoma |
title | Anticancer activity of streptochlorin, a novel antineoplastic agent, in cholangiocarcinoma |
title_full | Anticancer activity of streptochlorin, a novel antineoplastic agent, in cholangiocarcinoma |
title_fullStr | Anticancer activity of streptochlorin, a novel antineoplastic agent, in cholangiocarcinoma |
title_full_unstemmed | Anticancer activity of streptochlorin, a novel antineoplastic agent, in cholangiocarcinoma |
title_short | Anticancer activity of streptochlorin, a novel antineoplastic agent, in cholangiocarcinoma |
title_sort | anticancer activity of streptochlorin, a novel antineoplastic agent, in cholangiocarcinoma |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4404940/ https://www.ncbi.nlm.nih.gov/pubmed/25931814 http://dx.doi.org/10.2147/DDDT.S80205 |
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