STAT3 as a target for cancer drug discovery

被引:79
作者
Costantino, Luca [1 ]
Barlocco, Daniela [2 ]
机构
[1] Univ Modena & Reggio Emilia, Dipartimento Sci Farmaceut, I-41100 Modena, Italy
[2] Univ Milan, Ist Sci Farmaceut & Tossicol Pietro Pratesi, I-20133 Milan, Italy
关键词
antitumor agents; Stat-3; peptide-based antagonists; small molecules; natural compounds;
D O I
10.2174/092986708783955464
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Stat-3 ( Signal Transduction and Activator of Transcription) is a member of the Stat family of latent, cytosolic transcription factors that directly relate signals from the plasma membrane to the nucleus. This protein is constitutively activated by aberrant upstream tyrosine kinase activities in a broad spectrum of human tumors, and it has been identified as a promising target for cancer drug discovery. This review deals with the recent developments of peptides and peptidomimetics or even non-peptidic small molecules, able to bind to the SH2 domain of Stat-3, thus blocking its functions. Moreover, several compounds able to alter the Stat-3 pathway by inhibition of kinases upstream to Stat-3, or even with unknown targets, were reviewed.
引用
收藏
页码:834 / 843
页数:10
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