Resveratrol enhances radiation sensitivity in prostate cancer by inhibiting cell proliferation and promoting cell senescence and apoptosis

被引:101
作者
Fang, Yujiang [1 ,2 ]
DeMarco, Vincent G. [3 ,4 ]
Nicholl, Michael B. [1 ,2 ]
机构
[1] Univ Missouri, Sch Med, Dept Surg, Columbia, MO 65211 USA
[2] Univ Missouri, Sch Med, Ellis Fischel Canc Ctr, Columbia, MO USA
[3] Univ Missouri, Sch Med, Dept Internal Med, Columbia, MO USA
[4] Univ Missouri, Sch Med, Dept Med Physiol & Pharmacol, Columbia, MO USA
关键词
MUTANT P53 EXPRESSION; MOLECULAR-MECHANISMS; DOWN-REGULATION; TGF-BETA; SENSITIZATION; TRAIL; INTEGRATION; GAMMA-H2AX; RECEPTOR; P21;
D O I
10.1111/j.1349-7006.2012.02272.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Radiation therapy (XRT) for treatment of localized prostate cancer (PCA) has outcomes similar to surgery and medical therapy. Toxicities of XRT and the relative radioresistance of PCA limit the effectiveness of this treatment method. Safe and effective radiosensitizing agents are lacking to enhance the effectiveness for XRT for PCA. In this study, the effect of XRT in combination with the radiosensitizing agent resveratrol (RSV) was investigated in a radioresistant PCA cell line, PC-3. Our results show the addition of RSV to XRT (XRT/RSV) synergistically enhanced XRT-induced apoptosis and inhibition of PC-3 proliferation. The antiproliferative effect of XRT/RSV treatment correlated with increased expression of p15, p21, and mutant p53 and decreased expression of cyclin B, cyclin D, and cdk2. Increased apoptosis correlated with increased expression of Fas and TRAILR1. Furthermore, XRT/RSV had little effect on the expression of p-AKT, whereas it increased the expression level of p-H2A.X, a marker for senescence. These data highlight the potential of RSV as a radiation sensitizer for PCA treatment and warrant further investigation. (Cancer Sci 2012; 103: 10901098)
引用
收藏
页码:1090 / 1098
页数:9
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