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(−)-Gossypol Inhibits Growth and Promotes Apoptosis of Human Head and Neck Squamous Cell Carcinoma In Vivo

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
Source :
Neoplasia: An International Journal for Oncology Research, Vol 8, Iss 3, Pp 163-172 (2006)
Publication Year :
2006
Publisher :
Elsevier, 2006.

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.

Details

Language :
English
ISSN :
14765586 and 15228002
Volume :
8
Issue :
3
Database :
Directory of Open Access Journals
Journal :
Neoplasia: An International Journal for Oncology Research
Publication Type :
Academic Journal
Accession number :
edsdoj.8e746646c88343ee89054732a337a711
Document Type :
article
Full Text :
https://doi.org/10.1593/neo.05691