Antibody ligation of CM1 on cisplatin-exposed HeLa cells induces apoptosis through reactive oxygen species-dependent Fas ligand expression

被引:2
作者
Park, Ga Bin [1 ,2 ]
Kim, Daejin [1 ,2 ]
Yoon, Hoi Soo [1 ,2 ]
Kim, Yeong-Seok [1 ,2 ]
Lee, Hyun-Kyung [3 ]
Kim, Ki Tae [4 ]
Jeong, Dae Hoon [4 ]
Hur, Dae Young [4 ]
机构
[1] Inje Univ, Coll Med, Dept Anat, Pusan 614735, South Korea
[2] Inje Univ, Coll Med, Res Ctr Woman Dis, Pusan 614735, South Korea
[3] Inje Univ, Busan Paik Hosp, Dept Internal Med, Pusan 614735, South Korea
[4] Inje Univ, Busan Paik Hosp, Dept Obstet & Gynecol, Pusan 614735, South Korea
关键词
cisplatin; HeLa cells; ROS; Fas ligand; CM1; CANCER-CELLS; CERVICAL-CANCER; UP-REGULATION; C-JUN; RESISTANCE; ACTIVATION; MECHANISMS; GROWTH; DEATH;
D O I
10.3892/ijo.2014.2361
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Centrocyte/centroblast marker 1 (CM1) has been identified as a pro-apoptosis molecule on B-cell lymphoma cells as well as several types of cancer cells. In this study, we investigated its signaling mechanism in He La cells after treatment with cisplatin in order to potentially identify a new therapeutic target. The CM1 molecule was induced on the surface of cisplatin-exposed He La cells. In these cells, ligation of CM1 with anti-CM1 monoclonal antibodies inhibited cell proliferation and produced reactive oxygen species. Fas ligand (FasL) expression was upregulated without upregulating Fas in cisplatin-exposed He La cells after CM1 stimulation. Pretreatment with N-acetylcysteine, a pan-capase inhibitor, and ZB4, an antagonistic anti-Fas antibody, effectively inhibited the apoptotic effect triggered by CM1. CM1 ligation induced apoptosis through disruption of the mitochondrial membrane potential, decreased Bcl-2 and phosphorylated ERK expression. These findings identify CM1 as a potential new therapeutic target related to cisplatin-exposed cervical cancer.
引用
收藏
页码:2016 / 2024
页数:9
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