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Antitumor activity and macrophage nitric oxide producing action of medicinal herb, Crassocephalum crepidioides

BACKGROUND: Crassocephalum crepidioides, a plant distributed in Okinawa Islands, is known in folk medicine; however, its anticancer activity has not been investigated. The aim of this study was to determine the in vitro and in vivo antitumor activities of C. crepidioides on murine Sarcoma 180 (S-180...

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Autores principales: Tomimori, Koh, Nakama, Shinji, Kimura, Ryuichiro, Tamaki, Kazumi, Ishikawa, Chie, Mori, Naoki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3407475/
https://www.ncbi.nlm.nih.gov/pubmed/22720874
http://dx.doi.org/10.1186/1472-6882-12-78
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author Tomimori, Koh
Nakama, Shinji
Kimura, Ryuichiro
Tamaki, Kazumi
Ishikawa, Chie
Mori, Naoki
author_facet Tomimori, Koh
Nakama, Shinji
Kimura, Ryuichiro
Tamaki, Kazumi
Ishikawa, Chie
Mori, Naoki
author_sort Tomimori, Koh
collection PubMed
description BACKGROUND: Crassocephalum crepidioides, a plant distributed in Okinawa Islands, is known in folk medicine; however, its anticancer activity has not been investigated. The aim of this study was to determine the in vitro and in vivo antitumor activities of C. crepidioides on murine Sarcoma 180 (S-180) and related molecular mechanisms. METHODS: The antitumor effect of C. crepidioides was evaluated in S-180-cell-bearing mice. Cell growth was assessed using a colorimetric assay. Nitrite and nitrate levels were measured by colorimetry. The expression levels of inducible NO synthase (iNOS) in murine RAW264.7 macrophages was assessed by reverse transcriptase-polymerase chain reaction. Activation of iNOS promoter was detected by reporter gene. Activation of nuclear factor-κB (NF-κB) was evaluated by electrophoretic mobility shift assay. The role of NF-κB signaling was analyzed using inhibitors of NF-κB and dominant-negative mutants, and Western blot analysis. RESULTS: C. crepidioides extract delayed tumor growth in S-180-bearing mice. However, it did not inhibit S-180 cell growth in vitro. Supernatant of cultured C. crepidioides-stimulated RAW264.7 macrophages was cytotoxic to S-180 cells. This cytotoxicity was associated with nitric oxide (NO) production. NF-κB signaling pathway was crucial for the transcriptional activation of iNOS gene. Isochlorogenic acid, a component of C. crepidioides, induced NF-κB activation and iNOS expression. CONCLUSIONS: The results highlight the oncolytic and immunopotentiation properties of C. crepidioides mediated through NF-κB-induced release of NO from macrophages.
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spelling pubmed-34074752012-07-29 Antitumor activity and macrophage nitric oxide producing action of medicinal herb, Crassocephalum crepidioides Tomimori, Koh Nakama, Shinji Kimura, Ryuichiro Tamaki, Kazumi Ishikawa, Chie Mori, Naoki BMC Complement Altern Med Research Article BACKGROUND: Crassocephalum crepidioides, a plant distributed in Okinawa Islands, is known in folk medicine; however, its anticancer activity has not been investigated. The aim of this study was to determine the in vitro and in vivo antitumor activities of C. crepidioides on murine Sarcoma 180 (S-180) and related molecular mechanisms. METHODS: The antitumor effect of C. crepidioides was evaluated in S-180-cell-bearing mice. Cell growth was assessed using a colorimetric assay. Nitrite and nitrate levels were measured by colorimetry. The expression levels of inducible NO synthase (iNOS) in murine RAW264.7 macrophages was assessed by reverse transcriptase-polymerase chain reaction. Activation of iNOS promoter was detected by reporter gene. Activation of nuclear factor-κB (NF-κB) was evaluated by electrophoretic mobility shift assay. The role of NF-κB signaling was analyzed using inhibitors of NF-κB and dominant-negative mutants, and Western blot analysis. RESULTS: C. crepidioides extract delayed tumor growth in S-180-bearing mice. However, it did not inhibit S-180 cell growth in vitro. Supernatant of cultured C. crepidioides-stimulated RAW264.7 macrophages was cytotoxic to S-180 cells. This cytotoxicity was associated with nitric oxide (NO) production. NF-κB signaling pathway was crucial for the transcriptional activation of iNOS gene. Isochlorogenic acid, a component of C. crepidioides, induced NF-κB activation and iNOS expression. CONCLUSIONS: The results highlight the oncolytic and immunopotentiation properties of C. crepidioides mediated through NF-κB-induced release of NO from macrophages. BioMed Central 2012-06-21 /pmc/articles/PMC3407475/ /pubmed/22720874 http://dx.doi.org/10.1186/1472-6882-12-78 Text en Copyright ©2012 Tomimori et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Tomimori, Koh
Nakama, Shinji
Kimura, Ryuichiro
Tamaki, Kazumi
Ishikawa, Chie
Mori, Naoki
Antitumor activity and macrophage nitric oxide producing action of medicinal herb, Crassocephalum crepidioides
title Antitumor activity and macrophage nitric oxide producing action of medicinal herb, Crassocephalum crepidioides
title_full Antitumor activity and macrophage nitric oxide producing action of medicinal herb, Crassocephalum crepidioides
title_fullStr Antitumor activity and macrophage nitric oxide producing action of medicinal herb, Crassocephalum crepidioides
title_full_unstemmed Antitumor activity and macrophage nitric oxide producing action of medicinal herb, Crassocephalum crepidioides
title_short Antitumor activity and macrophage nitric oxide producing action of medicinal herb, Crassocephalum crepidioides
title_sort antitumor activity and macrophage nitric oxide producing action of medicinal herb, crassocephalum crepidioides
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3407475/
https://www.ncbi.nlm.nih.gov/pubmed/22720874
http://dx.doi.org/10.1186/1472-6882-12-78
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