(-)-Gossypol inhibits growth and promotes apoptosis of human head and neck squamous cell carcinoma in vivo

被引:105
作者
Wolter, Keith G.
Wang, Steven J.
Henson, Bradley S.
Wang, Shaomeng
Griffith, Kent A.
Kumar, Bhavna
Chen, Jianyong
Carey, Thomas E.
Bradford, Carol R.
D'Silva, Nisha J.
机构
[1] Univ Michigan, Sch Dent, Dept Periodont & Oral Med, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Dept Otolaryngol, Lab Head & Neck Canc Biol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Sch Med, Dept Surg, Sect Plast Surg, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Sch Med, Dept Surg, Dept Internal Med, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Ctr Comprehens Canc, Biostat Core, Ann Arbor, MI 48109 USA
来源
NEOPLASIA | 2006年 / 8卷 / 03期
关键词
chemoresistance; (-)-gossypol; head and neck cancer; oral cancer; Bcl-x(L);
D O I
10.1593/neo.05691
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 Bcl-x(L). (-)-Gossypol, the negative enantiomer of a cottonseed polyphenol, binds to Bcl-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 xenograft model of HNSCC, using two human HNSCC cell lines with high Bcl-x(L) 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.
引用
收藏
页码:163 / 172
页数:10
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