Targeting STAT3 with silibinin to improve cancer therapeutics

被引:94
作者
Bosch-Barrera, Joaquim [1 ,2 ,3 ]
Queralt, Bernardo [1 ,2 ,3 ]
Menendez, Javier A. [2 ,4 ]
机构
[1] Catalan Inst Oncol, Med Oncol, Girona, Catalonia, Spain
[2] Girona Biomed Res Inst IDIBGI, Girona, Catalonia, Spain
[3] Univ Girona, Med Sch, Dept Med Sci, Girona, Spain
[4] Catalan Inst Oncol, Metab & Canc Grp, ProCURE Program Canc Therapeut Resistance, Girona, Catalonia, Spain
关键词
Cancer; Silibinin; STAT3; Chemotherapy; Radiotherapy; Legasil (R); CELL LUNG-CANCER; TO-MESENCHYMAL TRANSITION; INDUCED GROWTH-INHIBITION; ACUTE MYELOID-LEUKEMIA; CARCINOMA DU145 CELLS; FACTOR-KAPPA-B; MILK THISTLE; DRUG-RESISTANCE; PROSTATE-CANCER; HEPATOCELLULAR-CARCINOMA;
D O I
10.1016/j.ctrv.2017.06.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Signal transducer and activator of transcription 3 (STAT3) has a prominent role in mediating resistance to conventional chemo-/radio-therapies and modern targeted drugs. While a number of STAT3 inhibitors have been shown to enhance the efficacy of therapeutic agents in vitro, the majority of them have yet to enter clinical evaluation mostly because of lack of efficacy issues. Silibinin is the main component of the silymarin complex, a standardized extract obtained from the seeds of the milk thistle herb Silybum marianum. This review summarizes current evidence supporting the ability of silibinin to function as a natural down-modulator of STAT3 activity. We examine the reported capacity of silibinin to reduce the toxicity of cancer treatments and to reverse tumor cell resistance via STAT3 inhibition. We also briefly review our clinical data in cancer patients treated with oral nutraceutical products containing silibinin. The beneficial effects of silibinin might accelerate the design of strategies aimed to overcome and prevent the emergence of STAT3-mediated cancer drug resistance in clinical settings. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:61 / 69
页数:9
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