Enhanced anticancer effect of gemcitabine by genistein in osteosarcoma: the role of Akt and nuclear factor-κB

被引:54
作者
Zhang, Bo [1 ]
Shi, Zhong-Li [2 ]
Liu, Bing [1 ]
Yan, Xiao-Bo [1 ]
Feng, Jie [2 ]
Tao, Hui-Min [1 ]
机构
[1] Zhejiang Univ, Dept Orthoped, Affiliated Hosp 2, Sch Med, Hangzhou 310009, Zhejiang, Peoples R China
[2] Zhejiang Univ, Inst Orthoped Res, Affiliated Hosp 2, Sch Med, Hangzhou 310009, Zhejiang, Peoples R China
关键词
Akt; apoptosis; gemcitabine; genistein; nuclear factor-kappa B; osteosarcoma; SOY ISOFLAVONE GENISTEIN; PHASE-II TRIAL; PANCREATIC-CANCER; IN-VITRO; CHEMOTHERAPEUTIC-AGENTS; MOLECULAR EVIDENCE; ANTITUMOR-ACTIVITY; BREAST-CANCER; CELL-LINES; INHIBITOR;
D O I
10.1097/CAD.0b013e328334da17
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Genistein, a nontoxic flavonoid compound, has potent antitumor activity in various cancer cell lines. This study was designed to investigate whether combination therapy with gemcitabine and genistein enhances antitumor efficacy in osteosarcoma cell lines (MG-63 and U2OS). Our results show that significant reduction in cell viability and corresponding induction of apoptosis were observed with combination treatment in both cell lines. On the molecular level, we found that gemcitabine alone can activate nuclear factor kappa B (NF-kappa B) in osteosarcoma, suggesting the potential mechanism of acquired chemoresistance. In contrast, genistein reversed the cancer's resistance to gemcitabine through the downregulation of NF-kappa B activity and the suppression of Akt. These findings suggest that the combination of gemcitabine and genistein enhanced the antitumor efficacy by abrogating the Akt/NF-kappa B pathway. The marked ability to induce apoptosis with a combination of gemcitabine and genistein suggests that this could be a rational and novel approach for osteosarcoma preclinical and clinical trials. Anti-Cancer Drugs 21: 288-296 (C) 2010 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
引用
收藏
页码:288 / 296
页数:9
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