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The combined anticancer of peanut skin procyanidins and resveratrol to CACO‐2 colorectal cancer cells

Colorectal cancer is one of the leading causes of cancer deaths worldwide. Currently, chemotherapy is the primary way for colorectal cancer, but with severe side effects. Therefore, it is urgent to find safer and more effective adjuvant treatment methods. At present, natural active substances are pr...

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Autores principales: Wang, Na, Gao, Enguang, Cui, Chenxu, Wang, Fan, Ren, Hongtao, Xu, Chao, Ning, Cancan, Zheng, Yuru, Liu, Qingqing, Yu, Qiuying, Zhang, Gaiping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563709/
https://www.ncbi.nlm.nih.gov/pubmed/37831732
http://dx.doi.org/10.1002/fsn3.3590
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author Wang, Na
Gao, Enguang
Cui, Chenxu
Wang, Fan
Ren, Hongtao
Xu, Chao
Ning, Cancan
Zheng, Yuru
Liu, Qingqing
Yu, Qiuying
Zhang, Gaiping
author_facet Wang, Na
Gao, Enguang
Cui, Chenxu
Wang, Fan
Ren, Hongtao
Xu, Chao
Ning, Cancan
Zheng, Yuru
Liu, Qingqing
Yu, Qiuying
Zhang, Gaiping
author_sort Wang, Na
collection PubMed
description Colorectal cancer is one of the leading causes of cancer deaths worldwide. Currently, chemotherapy is the primary way for colorectal cancer, but with severe side effects. Therefore, it is urgent to find safer and more effective adjuvant treatment methods. At present, natural active substances are promising alternatives, as numerous studies have demonstrated possible synergistic anticancer effects in plant‐active polyphenols. In the present study, the combined effect of procyanidins (PC) (from peanut skin) and resveratrol (RES) (from peanut buds) on the synergistic anticancer potential was investigated. CACO‐2 and HCT‐8 cells were served as colorectal cancer models, and HEPG‐2 and HUH‐7 cells were served as liver cancer models to observe the effects of PC and RES alone or in combination on the growth and proliferation of these four types of cancer cells. The results revealed that both PC and RES could inhibit the cells’ proliferation in a manner with concentration‐dependent, but they exerted synergistic anticancer effects only on CACO‐2 cells. PC and RES could synergistically inhibit CACO‐2 cell clone formation, inducing apoptosis of CACO‐2 cells and blocking their cell cycle in G0/G1 phase. Additionally, as observed by the results of Western blot assay, the combined effect of PC and RES also inhibited the phosphorylation of Thr308, Ser473, and ERK and promoted the phosphorylation of IKBα and NF‐κB in CACO‐2 cells. These findings collectively indicate that PC combined with RES might exert synergistic anticancer effects by regulating AKT, ERK, and NF‐κB signaling pathways.
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spelling pubmed-105637092023-10-11 The combined anticancer of peanut skin procyanidins and resveratrol to CACO‐2 colorectal cancer cells Wang, Na Gao, Enguang Cui, Chenxu Wang, Fan Ren, Hongtao Xu, Chao Ning, Cancan Zheng, Yuru Liu, Qingqing Yu, Qiuying Zhang, Gaiping Food Sci Nutr Original Articles Colorectal cancer is one of the leading causes of cancer deaths worldwide. Currently, chemotherapy is the primary way for colorectal cancer, but with severe side effects. Therefore, it is urgent to find safer and more effective adjuvant treatment methods. At present, natural active substances are promising alternatives, as numerous studies have demonstrated possible synergistic anticancer effects in plant‐active polyphenols. In the present study, the combined effect of procyanidins (PC) (from peanut skin) and resveratrol (RES) (from peanut buds) on the synergistic anticancer potential was investigated. CACO‐2 and HCT‐8 cells were served as colorectal cancer models, and HEPG‐2 and HUH‐7 cells were served as liver cancer models to observe the effects of PC and RES alone or in combination on the growth and proliferation of these four types of cancer cells. The results revealed that both PC and RES could inhibit the cells’ proliferation in a manner with concentration‐dependent, but they exerted synergistic anticancer effects only on CACO‐2 cells. PC and RES could synergistically inhibit CACO‐2 cell clone formation, inducing apoptosis of CACO‐2 cells and blocking their cell cycle in G0/G1 phase. Additionally, as observed by the results of Western blot assay, the combined effect of PC and RES also inhibited the phosphorylation of Thr308, Ser473, and ERK and promoted the phosphorylation of IKBα and NF‐κB in CACO‐2 cells. These findings collectively indicate that PC combined with RES might exert synergistic anticancer effects by regulating AKT, ERK, and NF‐κB signaling pathways. John Wiley and Sons Inc. 2023-08-03 /pmc/articles/PMC10563709/ /pubmed/37831732 http://dx.doi.org/10.1002/fsn3.3590 Text en © 2023 The Authors. Food Science & Nutrition published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Wang, Na
Gao, Enguang
Cui, Chenxu
Wang, Fan
Ren, Hongtao
Xu, Chao
Ning, Cancan
Zheng, Yuru
Liu, Qingqing
Yu, Qiuying
Zhang, Gaiping
The combined anticancer of peanut skin procyanidins and resveratrol to CACO‐2 colorectal cancer cells
title The combined anticancer of peanut skin procyanidins and resveratrol to CACO‐2 colorectal cancer cells
title_full The combined anticancer of peanut skin procyanidins and resveratrol to CACO‐2 colorectal cancer cells
title_fullStr The combined anticancer of peanut skin procyanidins and resveratrol to CACO‐2 colorectal cancer cells
title_full_unstemmed The combined anticancer of peanut skin procyanidins and resveratrol to CACO‐2 colorectal cancer cells
title_short The combined anticancer of peanut skin procyanidins and resveratrol to CACO‐2 colorectal cancer cells
title_sort combined anticancer of peanut skin procyanidins and resveratrol to caco‐2 colorectal cancer cells
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563709/
https://www.ncbi.nlm.nih.gov/pubmed/37831732
http://dx.doi.org/10.1002/fsn3.3590
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