(−)-gossypol inhibits growth and promotes apoptosis of human head and neck squamous cell carcinoma in vivo
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ID: 167841
2006
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Abstract
Resistance to chemotherapy is a common problem encountered in the treatment of head and neck squamous cell carcinoma (HNSCC). Chemoresistant HNSCC tumors frequently overexpress antiapoptotic proteins, such as BCI-xL. (−)-Gossypol, the negative enantiomer of a cottonseed polyphenol, binds to BCI-xL and was recently been shown to inhibit HNSCC proliferation in vitro. In this study, we assessed the in vivo efficacy of (−)-gossypol in an orthotopic xenograff model of HNSCC, using two human HNSCC cell lines with high BCI-xL expression levels. Both produced tumors in a murine floor-of-mouth model that mimics human HNSCC, exhibiting growth and invasion into adjacent tissues. Mice were randomized into three groups: vehicle control and two daily intraperitoneal (−)-gossypol treatment groups (5 and 15 mg/kg). Tumors were measured twice weekly. In the control group, tumors grew progressively, whereas in (−)-gossypol treatment groups, tumor growth was significantly suppressed. The mitotic rate in tumors from (−)-gossypol-treated animals was significantly lower than that in controls, and an increase in the percentage of apoptotic cells was observed in treated tumors versus controls. Residual tumors remained growth-suppressed for 2 weeks after cessation of (−)-gossypol treatment. Our results demonstrate that (−)-gossypol can inhibit tumor growth in an orthotopic model of aggressive HNSCC.
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| Reference Key |
wolter2006neoplasia:()-gossypol
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| Authors | ;Keith G. Wolter;Steven J. Wang;Bradley S. Henson;Shaomeng Wang;Kent A. Griffith;Bhavna Kumar;Jianyong Chen;Thomas E. Carey;Carol R. Bradford;Nisha J. D'Silva |
| Journal | ACS chemical neuroscience |
| Year | 2006 |
| DOI |
10.1593/neo.05691
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