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NOTCH信号通路作为一种新型癌症治疗靶点。

NOTCH signaling as a novel cancer therapeutic target.

作者信息

Miele L, Miao H, Nickoloff B J

机构信息

Cutaneous Oncology Program, Cardinal Bernardin Cancer Center and Departments of Pathology and Microbiology-Immunology, Loyola University Chicago, Maywood, IL 60153, USA.

出版信息

Curr Cancer Drug Targets. 2006 Jun;6(4):313-23. doi: 10.2174/156800906777441771.

Abstract

NOTCH-ligand interaction is a highly conserved mechanism that regulates specific cell fate decision during development. In addition to its functions in developmental and cell maturation processes, studies indicate that NOTCH activation plays a role in the onset and progression of many human malignancies. The prevailing new strategy for rationally targeted cancer treatment is aimed at the development of target-selective "smart" drugs on the basis of characterized mechanisms of action. The connection between NOTCH signaling and tumorigenesis suggests that NOTCH may be such a target candidate. Gamma-secretase is a large membrane-integral multisubunit protease complex, which is essential for NOTCH receptor activation. Inhibitors of this enzyme are being developed for Alzheimer's disease, due to its role in cleaving beta-amyloid precursor in the brain. Recently, Gamma-secretase inhibitors (GSIs), as well as various biopharmaceutical or genetic NOTCH signaling inhibitors have been suggested as potential novel cancer therapeutic strategies. This review summarizes the evidence linking NOTCH signaling to several types of cancer, as well as the possible therapeutic indications of NOTCH inhibitors and the challenges facing their clinical development.

摘要

NOTCH配体相互作用是一种高度保守的机制,在发育过程中调节特定的细胞命运决定。除了在发育和细胞成熟过程中的功能外,研究表明NOTCH激活在许多人类恶性肿瘤的发生和发展中起作用。合理靶向癌症治疗的主要新策略旨在基于已明确的作用机制开发靶向选择性的“智能”药物。NOTCH信号传导与肿瘤发生之间的联系表明NOTCH可能是这样一个候选靶点。γ-分泌酶是一种大型膜整合多亚基蛋白酶复合体,对NOTCH受体激活至关重要。由于其在大脑中切割β-淀粉样前体蛋白的作用,该酶的抑制剂正在被开发用于治疗阿尔茨海默病。最近,γ-分泌酶抑制剂(GSIs)以及各种生物制药或基因NOTCH信号传导抑制剂已被提议作为潜在的新型癌症治疗策略。这篇综述总结了将NOTCH信号传导与几种癌症类型联系起来的证据,以及NOTCH抑制剂可能的治疗适应症和其临床开发面临的挑战。

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