Perifosine sensitizes curcumin-induced anti-colorectal cancer effects by targeting multiple signaling pathways both in vivo and in vitro

被引:42
作者
Chen, Min-Bin [2 ]
Wu, Xiao-Yang [3 ]
Tao, Guo-Qing [1 ]
Liu, Chao-Ying [4 ]
Chen, Jian [3 ]
Wang, Li-Qiang [2 ]
Lu, Pei-Hua [1 ]
机构
[1] Nanjing Med Univ, Affiliated Wuxi Peoples Hosp, Dept Gen Surg, Ctr Oncol, Wuxi 214023, Jiangsu, Peoples R China
[2] Jiangsu Univ, Kunshan Peoples Hosp 1, Dept Med Oncol, Kunshan, Jiangsu, Peoples R China
[3] Jiangsu Univ, Kunshan Peoples Hosp 1, Dept Gen Surg, Kunshan, Jiangsu, Peoples R China
[4] Nanjing Med Univ, Affiliated Wuxi Peoples Hosp, Dept Med Oncol, Ctr Oncol, Wuxi 214023, Jiangsu, Peoples R China
关键词
perifosine; curcumin; colorectal cancer; apoptosis; signal transduction; NF-KAPPA-B; ENDOPLASMIC-RETICULUM STRESS; LEUKEMIA-CELLS; ALKYL-LYSOPHOSPHOLIPIDS; ANTITUMOR-ACTIVITY; INHIBITION; APOPTOSIS; AKT; EXPRESSION; GROWTH;
D O I
10.1002/ijc.27548
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Our study shows that coadministration of curcumin and an orally bioactive alkylphospholipid perifosine results in a significant increase in colorectal cancer cell apoptosis and a marked inhibition of cell growth both in vitro and in vivo. This novel combinatorial regimen leads to changes of multiple cell signaling pathways including inactivation of Akt and nuclear factor-?B as well as activation of c-Jun N-terminal kinases and endoplasmic reticulum stress. Further, perifosine and curcumin synergistically increase intracellular level of reactive oxygen species and ceramide, and downregulate the expression of cyclin D1 and Bcl-2 in colorectal cancer cells. These changes at molecular level together account for the cancer cell apoptosis and growth inhibition. We conclude that perifosine sensitizes colorectal cancer cells to curcumin by modulating multiple signaling pathways. Adding perifosine with curcumin may represent an effective therapy regimen against colorectal cancers, and possible other aggressive tumors.
引用
收藏
页码:2487 / 2498
页数:12
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