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Synergistic inhibitory effects of cetuximab and curcumin on human cisplatin-resistant oral cancer CAR cells through intrinsic apoptotic process

Cetuximab, an epidermal growth factor receptor (EGFR)-targeting monoclonal antibody (mAb), is a novel targeted therapy for the treatment of patients with oral cancer. Cetuximab can be used in combination with chemotherapeutic agents to prolong the overall survival rates of patients with oral cancer....

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Autores principales: Chen, Chin-Fu, Lu, Chi-Cheng, Chiang, Jo-Hua, Chiu, Hong-Yi, Yang, Jai-Sing, Lee, Chao-Ying, Way, Tzong-Der, Huang, Hao-Jen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176463/
https://www.ncbi.nlm.nih.gov/pubmed/30333889
http://dx.doi.org/10.3892/ol.2018.9418
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author Chen, Chin-Fu
Lu, Chi-Cheng
Chiang, Jo-Hua
Chiu, Hong-Yi
Yang, Jai-Sing
Lee, Chao-Ying
Way, Tzong-Der
Huang, Hao-Jen
author_facet Chen, Chin-Fu
Lu, Chi-Cheng
Chiang, Jo-Hua
Chiu, Hong-Yi
Yang, Jai-Sing
Lee, Chao-Ying
Way, Tzong-Der
Huang, Hao-Jen
author_sort Chen, Chin-Fu
collection PubMed
description Cetuximab, an epidermal growth factor receptor (EGFR)-targeting monoclonal antibody (mAb), is a novel targeted therapy for the treatment of patients with oral cancer. Cetuximab can be used in combination with chemotherapeutic agents to prolong the overall survival rates of patients with oral cancer. Curcumin is a traditional Chinese medicine, and it has been demonstrated to have growth-inhibiting effects on oral cancer cells. However, information regarding the combination of cetuximab and curcumin in drug-resistant oral cancer cells is lacking, and its underlying mechanism remains unclear. The purpose of the present study was to explore the oral anticancer effects of cetuximab combined with curcumin on cisplatin-resistant oral cancer CAR cell apoptosis in vitro. The results demonstrated that combination treatment synergistically potentiated the effect of cetuximab and curcumin on the suppression of cell viability and induction of apoptosis in CAR cells. Cetuximab and curcumin combination induced apoptosis and dramatically increased caspase-3 and caspase-9 activities compared with singular treatment. Combination treatment also markedly suppressed the protein expression levels of EGFR and mitogen-activated protein kinases (MAPKs) signaling (phosphorylation of ERK, JNK and p38). The results demonstrated that co-treatment with cetuximab and curcumin exerts synergistic oral anticancer effects on CAR cells through the suppression of the EGFR signaling by regulation of the MAPK pathway.
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spelling pubmed-61764632018-10-17 Synergistic inhibitory effects of cetuximab and curcumin on human cisplatin-resistant oral cancer CAR cells through intrinsic apoptotic process Chen, Chin-Fu Lu, Chi-Cheng Chiang, Jo-Hua Chiu, Hong-Yi Yang, Jai-Sing Lee, Chao-Ying Way, Tzong-Der Huang, Hao-Jen Oncol Lett Articles Cetuximab, an epidermal growth factor receptor (EGFR)-targeting monoclonal antibody (mAb), is a novel targeted therapy for the treatment of patients with oral cancer. Cetuximab can be used in combination with chemotherapeutic agents to prolong the overall survival rates of patients with oral cancer. Curcumin is a traditional Chinese medicine, and it has been demonstrated to have growth-inhibiting effects on oral cancer cells. However, information regarding the combination of cetuximab and curcumin in drug-resistant oral cancer cells is lacking, and its underlying mechanism remains unclear. The purpose of the present study was to explore the oral anticancer effects of cetuximab combined with curcumin on cisplatin-resistant oral cancer CAR cell apoptosis in vitro. The results demonstrated that combination treatment synergistically potentiated the effect of cetuximab and curcumin on the suppression of cell viability and induction of apoptosis in CAR cells. Cetuximab and curcumin combination induced apoptosis and dramatically increased caspase-3 and caspase-9 activities compared with singular treatment. Combination treatment also markedly suppressed the protein expression levels of EGFR and mitogen-activated protein kinases (MAPKs) signaling (phosphorylation of ERK, JNK and p38). The results demonstrated that co-treatment with cetuximab and curcumin exerts synergistic oral anticancer effects on CAR cells through the suppression of the EGFR signaling by regulation of the MAPK pathway. D.A. Spandidos 2018-11 2018-09-07 /pmc/articles/PMC6176463/ /pubmed/30333889 http://dx.doi.org/10.3892/ol.2018.9418 Text en Copyright: © Chen et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Chen, Chin-Fu
Lu, Chi-Cheng
Chiang, Jo-Hua
Chiu, Hong-Yi
Yang, Jai-Sing
Lee, Chao-Ying
Way, Tzong-Der
Huang, Hao-Jen
Synergistic inhibitory effects of cetuximab and curcumin on human cisplatin-resistant oral cancer CAR cells through intrinsic apoptotic process
title Synergistic inhibitory effects of cetuximab and curcumin on human cisplatin-resistant oral cancer CAR cells through intrinsic apoptotic process
title_full Synergistic inhibitory effects of cetuximab and curcumin on human cisplatin-resistant oral cancer CAR cells through intrinsic apoptotic process
title_fullStr Synergistic inhibitory effects of cetuximab and curcumin on human cisplatin-resistant oral cancer CAR cells through intrinsic apoptotic process
title_full_unstemmed Synergistic inhibitory effects of cetuximab and curcumin on human cisplatin-resistant oral cancer CAR cells through intrinsic apoptotic process
title_short Synergistic inhibitory effects of cetuximab and curcumin on human cisplatin-resistant oral cancer CAR cells through intrinsic apoptotic process
title_sort synergistic inhibitory effects of cetuximab and curcumin on human cisplatin-resistant oral cancer car cells through intrinsic apoptotic process
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176463/
https://www.ncbi.nlm.nih.gov/pubmed/30333889
http://dx.doi.org/10.3892/ol.2018.9418
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