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Evaluation of anti-tumorigenic activity of BP3B against colon cancer with patient-derived tumor xenograft model

BACKGROUND: KIOM-CRC#BP3B (BP3B) is a novel herbal prescription that is composed of three plant extracts. Our preliminary study identified that BP3B exhibited potent anti-proliferative activity against various types of cancer cell lines in vitro. Because the in vivo anti-tumor effect of BP3B is not...

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Autores principales: Kim, Hye-Youn, Kim, Jinhee, Ha Thi, Huyen Trang, Bang, Ok-Sun, Lee, Won-Suk, Hong, Suntaek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116142/
https://www.ncbi.nlm.nih.gov/pubmed/27863496
http://dx.doi.org/10.1186/s12906-016-1447-8
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author Kim, Hye-Youn
Kim, Jinhee
Ha Thi, Huyen Trang
Bang, Ok-Sun
Lee, Won-Suk
Hong, Suntaek
author_facet Kim, Hye-Youn
Kim, Jinhee
Ha Thi, Huyen Trang
Bang, Ok-Sun
Lee, Won-Suk
Hong, Suntaek
author_sort Kim, Hye-Youn
collection PubMed
description BACKGROUND: KIOM-CRC#BP3B (BP3B) is a novel herbal prescription that is composed of three plant extracts. Our preliminary study identified that BP3B exhibited potent anti-proliferative activity against various types of cancer cell lines in vitro. Because the in vivo anti-tumor effect of BP3B is not evaluated before clinical trial, we want to test it using patient’s samples. METHODS: To confirm the in vivo anti-cancer effect of BP3B, we used genetically characterized patient-derived colon tumor xenograft (PDTX) mouse model. Anti-cancer activity was evaluated with apoptosis, proliferation, angiogenesis and histological analysis. RESULTS: Oral administration of BP3B significantly inhibited the tumor growth in two PDTX models. Furthermore, TUNEL assay showed that BP3B induced apoptosis of tumor tissues, which was associated with degradation of PARP and Caspase 8 and activation of Caspase 3. We also observed that BP3B inhibited cancer cell proliferation by down-regulation of Cyclin D1 and induction of p27 proteins. Inhibition of angiogenesis in BP3B-treated group was observed with immunofluorescence staining using CD31 and Tie-2 antibodies. CONCLUSION: These findings indicated that BP3B has a strong growth-inhibitory activity against colon cancer in in vivo model and will be a good therapeutic candidate for treatment of refractory colon cancer. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12906-016-1447-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-51161422016-11-25 Evaluation of anti-tumorigenic activity of BP3B against colon cancer with patient-derived tumor xenograft model Kim, Hye-Youn Kim, Jinhee Ha Thi, Huyen Trang Bang, Ok-Sun Lee, Won-Suk Hong, Suntaek BMC Complement Altern Med Research Article BACKGROUND: KIOM-CRC#BP3B (BP3B) is a novel herbal prescription that is composed of three plant extracts. Our preliminary study identified that BP3B exhibited potent anti-proliferative activity against various types of cancer cell lines in vitro. Because the in vivo anti-tumor effect of BP3B is not evaluated before clinical trial, we want to test it using patient’s samples. METHODS: To confirm the in vivo anti-cancer effect of BP3B, we used genetically characterized patient-derived colon tumor xenograft (PDTX) mouse model. Anti-cancer activity was evaluated with apoptosis, proliferation, angiogenesis and histological analysis. RESULTS: Oral administration of BP3B significantly inhibited the tumor growth in two PDTX models. Furthermore, TUNEL assay showed that BP3B induced apoptosis of tumor tissues, which was associated with degradation of PARP and Caspase 8 and activation of Caspase 3. We also observed that BP3B inhibited cancer cell proliferation by down-regulation of Cyclin D1 and induction of p27 proteins. Inhibition of angiogenesis in BP3B-treated group was observed with immunofluorescence staining using CD31 and Tie-2 antibodies. CONCLUSION: These findings indicated that BP3B has a strong growth-inhibitory activity against colon cancer in in vivo model and will be a good therapeutic candidate for treatment of refractory colon cancer. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12906-016-1447-8) contains supplementary material, which is available to authorized users. BioMed Central 2016-11-18 /pmc/articles/PMC5116142/ /pubmed/27863496 http://dx.doi.org/10.1186/s12906-016-1447-8 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Kim, Hye-Youn
Kim, Jinhee
Ha Thi, Huyen Trang
Bang, Ok-Sun
Lee, Won-Suk
Hong, Suntaek
Evaluation of anti-tumorigenic activity of BP3B against colon cancer with patient-derived tumor xenograft model
title Evaluation of anti-tumorigenic activity of BP3B against colon cancer with patient-derived tumor xenograft model
title_full Evaluation of anti-tumorigenic activity of BP3B against colon cancer with patient-derived tumor xenograft model
title_fullStr Evaluation of anti-tumorigenic activity of BP3B against colon cancer with patient-derived tumor xenograft model
title_full_unstemmed Evaluation of anti-tumorigenic activity of BP3B against colon cancer with patient-derived tumor xenograft model
title_short Evaluation of anti-tumorigenic activity of BP3B against colon cancer with patient-derived tumor xenograft model
title_sort evaluation of anti-tumorigenic activity of bp3b against colon cancer with patient-derived tumor xenograft model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116142/
https://www.ncbi.nlm.nih.gov/pubmed/27863496
http://dx.doi.org/10.1186/s12906-016-1447-8
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