The sphingosine kinase 2 inhibitor ABC294640 inhibits cervical carcinoma cell growth
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Ling Xu1,*, Longmei Jin2,*, Baohua Yang1,*, Lifeng Wang1, Ziyin Xia1, Qian Zhang3 and Jun Xu1
1Department of Obstetrics and Gynecology, Minhang Branch, Zhongshan Hospital, Fudan University, Shanghai, China
2Minhang District Maternal and Child Health Hospital, Shanghai, China
3Department of Medicinal Chemistry, School of Pharmacy, Fudan University, Shanghai, China
Jun Xu, email: firstname.lastname@example.org
Qian Zhang, email: email@example.com
Keywords: cervical carcinoma; sphingosine kinase 2; ABC294640; Bcl-2; ceramide
Received: October 26, 2017 Accepted: December 05, 2017 Published: December 19, 2017
ABC294640 is a specific sphingosine kinase 2 (SphK2) inhibitor. The anti-cervical carcinoma activity by ABC294640 was tested in this study. ABC294640 inhibited in vitro 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. In vivo, 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.
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