Xu Ling, Jin Longmei, Yang Baohua, Wang Lifeng, Xia Ziyin, Zhang Qian, Xu Jun
Department of Obstetrics and Gynecology, Minhang Branch, Zhongshan Hospital, Fudan University, Shanghai, China.
Minhang District Maternal and Child Health Hospital, Shanghai, China.
Oncotarget. 2017 Dec 19;9(2):2384-2394. doi: 10.18632/oncotarget.23415. eCollection 2018 Jan 5.
ABC294640 is a specific sphingosine kinase 2 (SphK2) inhibitor. The anti-cervical carcinoma activity by ABC294640 was tested in this study. ABC294640 inhibited growth of the established (C33A and HeLa lines) and primary human cervical carcinoma cells. The SphK2 inhibitor also induced G1-S arrest and apoptosis in cervical carcinoma cells. It was yet non-cytotoxic to SphK2-low human cervical epithelial cells. ABC294640 inhibited SphK activation, causing sphingosine-1-phosphate depletion, signal transducer and activator of transcription 3 in-activation and ceramide production. Bcl-2 is a key resistance factor of ABC294640. Pharmacological Bcl-2 inhibition or Bcl-2 shRNA potentiated ABC294640-induced C33A cell growth inhibition and apoptosis. On the other hand, exogenous over-expression of Bcl-2 attenuated ABC294640's cytotoxicity against C33A cells. , ABC294640 administration inhibited C33A xenograft tumor growth in mice. Co-administration of the Bcl-2 inhibitor GDC-0199 further potentiated ABC294640's anti-tumor activity. Together, we suggest that ABC294640 might have translational value for the treatment of human cervical carcinoma.
ABC294640是一种特异性的鞘氨醇激酶2(SphK2)抑制剂。本研究检测了ABC294640的抗宫颈癌活性。ABC294640抑制已建立的(C33A和HeLa细胞系)及原代人宫颈癌细胞的生长。这种SphK2抑制剂还可诱导宫颈癌细胞发生G1-S期阻滞和凋亡。它对SphK2表达水平低的人宫颈上皮细胞无细胞毒性。ABC294640抑制SphK激活,导致1-磷酸鞘氨醇耗竭、信号转导子和转录激活子3失活以及神经酰胺生成。Bcl-2是ABC294640的关键耐药因子。药理学抑制Bcl-2或Bcl-2短发夹RNA可增强ABC294640诱导的C33A细胞生长抑制和凋亡。另一方面,外源性过表达Bcl-2可减弱ABC294640对C33A细胞的细胞毒性。此外,给予ABC294640可抑制小鼠体内C33A异种移植瘤的生长。联合给予Bcl-2抑制剂GDC-0199可进一步增强ABC294640的抗肿瘤活性。综上所述,我们认为ABC294640可能对人类宫颈癌的治疗具有转化应用价值。