Characterization of dihydroartemisinin-resistant colon carcinoma HCT116/R cell line

被引:22
|
作者
Lu, Jin-Jian [1 ,2 ]
Chen, Si-Meng [1 ]
Ding, Jian [1 ]
Meng, Ling-Hua [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Mat Med, Div Antitumor Pharmacol, State Key Lab Drug Res, Shanghai 201203, Peoples R China
[2] Zhejiang Chinese Med Univ, Coll Life Sci, Hangzhou 310053, Zhejiang, Peoples R China
关键词
Dihydroartemisinin; Resistant; Proteomics; Anti-tumor; HCT116; PANCREATIC-CANCER CELLS; OVARIAN-CANCER; IN-VITRO; BORTEZOMIB RESISTANCE; MULTIDRUG-RESISTANCE; PLATINUM-RESISTANCE; PROTEOMIC ANALYSIS; LEUKEMIA-CELLS; ARTEMISININ; APOPTOSIS;
D O I
10.1007/s11010-011-1072-2
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dihydroartemisinin (DHA) is an important artemisinin derivative and presents profound anti-tumor potential. A DHA-resistant cell line named HCT116/R derived from colon carcinoma cell line HCT116 was established in our previous study. Herein, we found that HCT116/R cells were much more resistant to DHA- or artesunate-induced proliferation inhibition and more tolerant to DHA-induced cell cycle arrest and apoptosis compared with those of the parent HCT116 cells. The protein levels of P-glycoprotein and MDR-associated protein 1 and the accumulation of doxorubicin in cells were similar in both cell lines. Moreover, HCT116/R cells were still sensitive to camptothecin- and doxorubicin-induced cell growth inhibition. To further explore the characterization of HCT116/R cell line, a proteomic study employing two-dimensional gel electrophoresis and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry was performed. Eight different expressed proteins between the two cell lines were identified including some heat shock proteins, annexins, etc. This study not only indicates that exposure to DHA may not induce a tumor multi-drug-resistant phenotype but also affords new clues for the further investigation of the anti-cancer mechanisms of DHA and other artemisinin derivatives.
引用
收藏
页码:329 / 337
页数:9
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