Utilization of arsenic trioxide as a treatment of cisplatin-resistant non-small cell lung cancer PC-9/CDDP and PC-14/CDDP cells

被引:11
作者
Suzuki, Toshihiro [1 ]
Ishibashi, Kenichi [1 ]
Yumoto, Atsushi [1 ]
Nishio, Kazuto [2 ]
Ogasawara, Yuki [1 ]
机构
[1] Meiji Pharmaceut Univ, Dept Analyt Biochem, Tokyo 2048588, Japan
[2] Kinki Univ, Dept Genome Biol, Osaka, Osaka 5898511, Japan
基金
日本学术振兴会;
关键词
cisplatin resistance; arsenic trioxicle; glutathione; adenosine triphosphate-binding cassette subfamily C transporter; GAMMA-GLUTAMYLCYSTEINE SYNTHETASE; MULTIDRUG-RESISTANCE; OVARIAN-CANCER; TRANSPORT; PUMP;
D O I
10.3892/ol.2015.3352
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cisplatin is a commonly used drug in combination chemotherapy. However, various malignant tumors frequently acquire resistance to cisplatin. Arsenic trioxide (ATO) has been approved as a chemotherapeutic drug for the treatment of acute promyelocytic leukemia, and the combination of ATE) and cisplatin has been revealed to demonstrate synergistic effects in ovarian and small cell lung cancer cells. Thus, it was hypothesized that ATO may also be active against cisplatin-resistant non-small cell lung cancer (NSCLC) PC-9/CDDP and PC-114./CDDP cells. The present study also evaluated the effects of ATO on the cisplatin-sensitive NSCLC PC-9 and PC-14 cell lines. Notably, ATO demonstrated a markedly decreased IC in the cisplatin-resistant PC-9/CDDP and PC-14/CDDP cells compared with the IC in the cisplatiri-sensitive parental PC-9 and PC-14 cells. Additionally, it was found that arsenite accumulation in the PC-9 cell line was affected through the downregulation of GS -X pump systems. Although it is likely that cisplatin resistance in PC-9 cells does not depend on the GS-X pump systems, ATE) was effective against cisplatin-resistant NSCLC PC-9/CDDP and PC-14/CDDP cells in combination chemotherapy.
引用
收藏
页码:805 / 809
页数:5
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