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

被引:35
作者
Chen, Chin-Fu [1 ]
Lu, Chi-Cheng [2 ]
Chiang, Jo-Hua [3 ]
Chiu, Hong-Yi [2 ]
Yang, Jai-Sing [4 ]
Lee, Chao-Ying [5 ]
Way, Tzong-Der [6 ]
Huang, Hao-Jen [1 ,7 ]
机构
[1] Natl Cheng Kung Univ, Dept Life Sci, 1 Univ Rd, Tainan 701, Taiwan
[2] Buddhist Tzu Chi Gen Hosp, Dept Pharm, Hualien 970, Taiwan
[3] Chung Jen Catholic Jr Coll, Dept Nursing, Chiayi 622, Chiayi County, Taiwan
[4] China Med Univ, China Med Univ Hosp, Dept Med Res, Taichung, Taiwan
[5] China Med Univ, Dept Pharm, Taichung 404, Taiwan
[6] China Med Univ, Dept Biol Sci & Technol, 91 Hsueh Shih Rd, Taichung 404, Taiwan
[7] Natl Cheng Kung Univ, Inst Trop Plant Sci, Tainan 701, Taiwan
关键词
cetuximab; curcumin; epidermal growth factor receptor; MAPK signaling; cisplatin-resistant oral cancer CAR cells; GROWTH-FACTOR RECEPTOR; TARGETING MONOCLONAL-ANTIBODIES; ENDOPLASMIC-RETICULUM STRESS; MOLECULAR TARGETS; IN-VITRO; HEAD; CARCINOMA; EGFR; THERAPY; DEATH;
D O I
10.3892/ol.2018.9418
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
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.
引用
收藏
页码:6323 / 6330
页数:8
相关论文
共 62 条
[11]
Effect of bis(hydroxymethyl) alkanoate curcuminoid derivative MTH-3 on cell cycle arrest, apoptotic and autophagic pathway in triple-negative breast adenocarcinoma MDA-MB-231 cells: an in vitro study [J].
Chang, Ling-Chu ;
Hsieh, Min-Tsang ;
Yang, Jai-Sing ;
Lu, Chi-Cheng ;
Tsai, Fuu-Jen ;
Tsao, Je-Wei ;
Chiu, Yu-Jen ;
Kuo, Sheng-Chu ;
Lee, Kuo-Hsiung .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2018, 52 (01) :67-76
[12]
Curcumin-loaded nanoparticles induce apoptotic cell death through regulation of the function of MDR1 and reactive oxygen species in cisplatin-resistant CAR human oral cancer cells [J].
Chang, Pei-Ying ;
Peng, Shu-Fen ;
Lee, Chao-Ying ;
Lu, Chi-Cheng ;
Tsai, Shih-Chang ;
Shieh, Tzong-Ming ;
Wu, Tian-Shung ;
Tu, Ming-Gene ;
Chen, Michael Yuanchien ;
Yang, Jai-Sing .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2013, 43 (04) :1141-1150
[13]
Progresses in TCM Metal-Based Antitumour Agents [J].
Chen, Zhen-Feng ;
Liang, Hong .
ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY, 2010, 10 (05) :412-423
[14]
Newly synthesized quinazolinone HMJ-38 suppresses angiogenetic responses and triggers human umbilical vein endothelial cell apoptosis through p53-modulated Fas/death receptor signaling [J].
Chiang, Jo-Hua ;
Yang, Jai-Sing ;
Lu, Chi-Cheng ;
Hour, Mann-Jen ;
Chang, Shu-Jen ;
Lee, Tsung-Han ;
Chung, Jing-Gung .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2013, 269 (02) :150-162
[15]
Cetuximab inhibits oral squamous cell carcinoma invasion and metastasis via degradation of epidermal growth factor receptor [J].
Dai, Wei ;
Li, Yanshu ;
Zhou, Qing ;
Xu, Zhongfei ;
Sun, Changfu ;
Tan, Xuexin ;
Lu, Li .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 2014, 43 (04) :250-257
[16]
Cisplatin in cancer therapy: Molecular mechanisms of action [J].
Dasari, Shaloam ;
Tchounwou, Paul Bernard .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2014, 740 :364-378
[17]
Targeting miRNAs by polyphenols: Novel therapeutic strategy for cancer [J].
Devi, Kasi Pandima ;
Rajavel, Tamilselvam ;
Daglia, Maria ;
Nabavi, Seyed Fazel ;
Bishayee, Anupam ;
Nabavi, Seyed Mohammad .
SEMINARS IN CANCER BIOLOGY, 2017, 46 :146-157
[18]
Beyond Yellow Curry: Assessing Commercial Curcumin Absorption Technologies [J].
Douglass, Brad J. ;
Clouatre, Dallas L. .
JOURNAL OF THE AMERICAN COLLEGE OF NUTRITION, 2015, 34 (04) :347-358
[19]
Molecular targets for anticancer redox chemotherapy and cisplatin-induced ototoxicity: the role of curcumin on pSTAT3 and Nrf-2 signalling [J].
Fetoni, A. R. ;
Paciello, F. ;
Mezzogori, D. ;
Rolesi, R. ;
Eramo, S. L. M. ;
Paludetti, G. ;
Troiani, D. .
BRITISH JOURNAL OF CANCER, 2015, 113 (10) :1434-1444
[20]
Acquired cisplatin resistance in the head-neck cancer cell line Cal27 is associated with decreased DKK1 expression and can partially be reversed by overexpression of DKK1 [J].
Gosepath, Eva M. ;
Eckstein, Niels ;
Hamacher, Alexandra ;
Servan, Kati ;
von Jonquieres, Georg ;
Lage, Hermann ;
Gyoerffy, Balazs ;
Royer, Hans D. ;
Kassack, Matthias U. .
INTERNATIONAL JOURNAL OF CANCER, 2008, 123 (09) :2013-2019