Curcumin sensitizes human lung cancer cells to apoptosis and metastasis synergistically combined with carboplatin

被引:58
作者
Kang, Ji Ho [1 ]
Kang, Hye Seon [1 ]
Kim, In Kyoung [1 ]
Lee, Hwa Young [1 ]
Ha, Jick Hwan [1 ]
Yeo, Chang Dong [1 ]
Kang, Hyun Hui [1 ]
Moon, Hwa Sik [1 ]
Lee, Sang Haak [1 ]
机构
[1] Catholic Univ Korea, Div Pulm Crit Care & Sleep Med, Dept Internal Med, Coll Med, Seoul 137701, South Korea
关键词
Curcumin; carboplatin; synergism; lung neoplasm; proliferation; NF-KAPPA-B; MOLECULAR-MECHANISMS; PLATINUM DRUGS; INHIBITION; KINASE; CHEMOTHERAPY; CARCINOMA; INDUCTION; CISPLATIN; PATHWAY;
D O I
10.1177/1535370215571881
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Although carboplatin is one of the standard chemotherapeutic agents for non-small cell lung cancer (NSCLC), it has limited therapeutic efficacy due to activation of a survival signaling pathway and the induction of multidrug resistance. Curcumin, a natural compound isolated from the plant Curcuma longa, is known to sensitize tumors to different chemotherapeutic agents. The aim of this study is to evaluate whether curcumin can chemosensitize lung cancer cells to carboplatin and to analyze the signaling pathway underlying this synergism. We investigated the synergistic effect of both agents on cell proliferation, apoptosis, invasion, migration, and expression of related signaling proteins using the human NSCLC cell line, A549. A549 cell was treated with different concentrations of curcumin and carboplatin alone and in combination. Combined treatment with curcumin and carboplatin inhibited tumor cell growth, migration, and invasion compared with either drug alone. Matrix metalloproteinase (MMP)-2 and MMP-9 were more efficiently downregulated by co-treatment than by each treatment alone. mRNA and protein expression of caspase-3 and caspase-9 and proapoptotic genes was increased in cells treated with a combination of curcumin and carboplatin, whereas expression of the antiapoptotic Bcl-2 gene was suppressed. Co-treatment of both agents substantially suppressed NF-B activation and increased expression of p53. Phosphorylation of Akt, a protein upstream of NF-B, was reduced, resulting in inhibition of the degradation of inhibitor of B(IB), whereas the activity of extracellular signal-regulated kinase (ERK1/2) was enhanced. Our study demonstrated that the synergistic antitumor activity of curcumin combined with carboplatin is mediated by multiple mechanisms involving suppression of NF-B via inhibition of the Akt/IKK pathway and enhanced ERK1/2 activity. Based on this mechanism, curcumin has potential as a chemosensitizer for carboplatin in the treatment of patients with NSCLC.
引用
收藏
页码:1416 / 1425
页数:10
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