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血液系统恶性肿瘤中的凋亡抑制蛋白(IAP):分子机制和治疗机会。

Inhibitor of Apoptosis (IAP) proteins in hematological malignancies: molecular mechanisms and therapeutic opportunities.

机构信息

Institute for Experimental Cancer Research in Pediatrics, Goethe-University, Frankfurt, Germany.

出版信息

Leukemia. 2014 Jul;28(7):1414-22. doi: 10.1038/leu.2014.56. Epub 2014 Feb 3.

Abstract

Inhibitor of Apoptosis (IAP) proteins exert essential functions during tumorigenesis as well as treatment resistance by simultaneously blocking cell death pathways and promoting cell survival. As IAP proteins are typically aberrantly expressed in human cancers including hematological malignancies, they represent in principle promising targets for therapeutic interventions. There are currently exciting opportunities to rationally exploit the therapeutic targeting of IAP proteins for the treatment of leukemia and lymphoma. Further insights into the signaling pathways that are under the control of IAP proteins and into the specific IAP protein-dependent vulnerabilities of hematological neoplasms are expected to pave the avenue to novel treatment strategies.

摘要

凋亡抑制蛋白(IAP)在肿瘤发生以及治疗耐药中发挥重要作用,同时阻断细胞死亡途径并促进细胞存活。由于 IAP 蛋白通常在包括血液恶性肿瘤在内的人类癌症中异常表达,因此它们原则上代表了治疗干预的有希望的靶点。目前,合理利用 IAP 蛋白的治疗靶向治疗白血病和淋巴瘤具有令人兴奋的机会。进一步深入了解受 IAP 蛋白控制的信号通路以及血液恶性肿瘤中特定的 IAP 蛋白依赖性脆弱性,有望为新的治疗策略铺平道路。

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