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Geijigajakyak decoction inhibits the motility and tumorigenesis of colorectal cancer cells

BACKGROUND: Recent studies report that inflammatory diseases of the large intestine are associated with colorectal cancer. Geijigajakyak Decoction (GJD) has antispasmodic and anti-inflammatory effects on the gastrointestinal tract. Thus, in light of the connection between chronic bowel inflammation...

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Autores principales: Lee, Soong-in, Bae, Jeong A, Ko, Yoo-Seung, Lee, Kyoung-in, Kim, Hangun, Kim, Kyung Keun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986256/
https://www.ncbi.nlm.nih.gov/pubmed/27527352
http://dx.doi.org/10.1186/s12906-016-1281-z
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author Lee, Soong-in
Bae, Jeong A
Ko, Yoo-Seung
Lee, Kyoung-in
Kim, Hangun
Kim, Kyung Keun
author_facet Lee, Soong-in
Bae, Jeong A
Ko, Yoo-Seung
Lee, Kyoung-in
Kim, Hangun
Kim, Kyung Keun
author_sort Lee, Soong-in
collection PubMed
description BACKGROUND: Recent studies report that inflammatory diseases of the large intestine are associated with colorectal cancer. Geijigajakyak Decoction (GJD) has antispasmodic and anti-inflammatory effects on the gastrointestinal tract. Thus, in light of the connection between chronic bowel inflammation and colorectal cancer (CRC), we asked whether GJD inhibits colorectal tumorigenesis. METHODS: The effects of GJD on the viability and proliferation of CRC cells were evaluated using MTT and BrdU assays, respectively. The motility of CRC cells was examined by a Transwell migration/invasion assay and immunoblot analysis was used to examine the signaling pathways associated with migration. A syngeneic Balb/c mice allograft model, in which CT26 cells were injected into the dorsum, was used to evaluate the anti-tumor effects of GJD in vivo. RESULTS: GJD had no cytotoxic effects against HCT116 CRC cells, although it did inhibit their proliferation. GJD inhibited the migration of HCT116 cells, and suppressed the invasion of HCT116, Caco2, and CSC221 CRC cells. In addition, GJD downregulated the expression of p-JNK and p-p38 MAPK, which are downstream signaling molecules associated with invasiveness. Furthermore, oral administration of GJD (333 mg/kg, twice a day) inhibited tumor growth in a mouse xenograft model. CONCLUSIONS: GJD inhibited the motility of human CRC cells and suppressed tumorigenesis in a mouse model. These results suggest that GJD warrants further study as a potential adjuvant anti-cancer therapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12906-016-1281-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-49862562016-08-17 Geijigajakyak decoction inhibits the motility and tumorigenesis of colorectal cancer cells Lee, Soong-in Bae, Jeong A Ko, Yoo-Seung Lee, Kyoung-in Kim, Hangun Kim, Kyung Keun BMC Complement Altern Med Research Article BACKGROUND: Recent studies report that inflammatory diseases of the large intestine are associated with colorectal cancer. Geijigajakyak Decoction (GJD) has antispasmodic and anti-inflammatory effects on the gastrointestinal tract. Thus, in light of the connection between chronic bowel inflammation and colorectal cancer (CRC), we asked whether GJD inhibits colorectal tumorigenesis. METHODS: The effects of GJD on the viability and proliferation of CRC cells were evaluated using MTT and BrdU assays, respectively. The motility of CRC cells was examined by a Transwell migration/invasion assay and immunoblot analysis was used to examine the signaling pathways associated with migration. A syngeneic Balb/c mice allograft model, in which CT26 cells were injected into the dorsum, was used to evaluate the anti-tumor effects of GJD in vivo. RESULTS: GJD had no cytotoxic effects against HCT116 CRC cells, although it did inhibit their proliferation. GJD inhibited the migration of HCT116 cells, and suppressed the invasion of HCT116, Caco2, and CSC221 CRC cells. In addition, GJD downregulated the expression of p-JNK and p-p38 MAPK, which are downstream signaling molecules associated with invasiveness. Furthermore, oral administration of GJD (333 mg/kg, twice a day) inhibited tumor growth in a mouse xenograft model. CONCLUSIONS: GJD inhibited the motility of human CRC cells and suppressed tumorigenesis in a mouse model. These results suggest that GJD warrants further study as a potential adjuvant anti-cancer therapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12906-016-1281-z) contains supplementary material, which is available to authorized users. BioMed Central 2016-08-15 /pmc/articles/PMC4986256/ /pubmed/27527352 http://dx.doi.org/10.1186/s12906-016-1281-z 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
Lee, Soong-in
Bae, Jeong A
Ko, Yoo-Seung
Lee, Kyoung-in
Kim, Hangun
Kim, Kyung Keun
Geijigajakyak decoction inhibits the motility and tumorigenesis of colorectal cancer cells
title Geijigajakyak decoction inhibits the motility and tumorigenesis of colorectal cancer cells
title_full Geijigajakyak decoction inhibits the motility and tumorigenesis of colorectal cancer cells
title_fullStr Geijigajakyak decoction inhibits the motility and tumorigenesis of colorectal cancer cells
title_full_unstemmed Geijigajakyak decoction inhibits the motility and tumorigenesis of colorectal cancer cells
title_short Geijigajakyak decoction inhibits the motility and tumorigenesis of colorectal cancer cells
title_sort geijigajakyak decoction inhibits the motility and tumorigenesis of colorectal cancer cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986256/
https://www.ncbi.nlm.nih.gov/pubmed/27527352
http://dx.doi.org/10.1186/s12906-016-1281-z
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