Dcona M Michael, Morris Benjamin L, Ellis Keith C, Grossman Steven R
a Department of Internal Medicine , Virginia Commonwealth University , Richmond , VA , USA.
b Department of Human and Molecular Genetics , Virginia Commonwealth University , Richmond , VA , USA.
Cancer Biol Ther. 2017 Jun 3;18(6):379-391. doi: 10.1080/15384047.2017.1323586. Epub 2017 May 22.
C-terminal Binding Proteins (CtBP) 1 and 2 are oncogenic transcriptional co-regulators overexpressed in many cancer types, with their expression level correlating to worse prognostic outcomes and aggressive tumor features. CtBP negatively regulates the expression of many tumor suppressor genes, while coactivating genes that promote proliferation, epithelial-mesenchymal transition, and cancer stem cell self-renewal activity. In light of this evidence, the development of novel inhibitors that mitigate CtBP function may provide clinically actionable therapeutic tools. This review article focuses on the progress made in understanding CtBP structure, role in tumor progression, and discovery and development of CtBP inhibitors that target CtBP's dehydrogenase activity and other functions, with a focus on the theory and rationale behind the designs of current inhibitors. We provide insight into the future development and use of rational combination therapy that may further augment the efficacy of CtBP inhibitors, specifically addressing metastasis and cancer stem cell populations within tumors.
C 末端结合蛋白(CtBP)1 和 2 是致癌转录共调节因子,在许多癌症类型中过表达,其表达水平与较差的预后结果和侵袭性肿瘤特征相关。CtBP 负向调节许多肿瘤抑制基因的表达,同时共激活促进增殖、上皮-间质转化和癌症干细胞自我更新活性的基因。鉴于此证据,开发减轻 CtBP 功能的新型抑制剂可能提供临床可行的治疗工具。这篇综述文章重点关注在理解 CtBP 结构、在肿瘤进展中的作用以及靶向 CtBP 脱氢酶活性和其他功能的 CtBP 抑制剂的发现与开发方面所取得的进展,重点是当前抑制剂设计背后的理论和基本原理。我们深入探讨了合理联合治疗的未来发展和应用,这可能会进一步增强 CtBP 抑制剂的疗效,特别针对肿瘤内的转移和癌症干细胞群体。