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IAPs:从细胞胱冬酶抑制剂到 NF-κB、炎症和癌症的调节剂。

IAPs: from caspase inhibitors to modulators of NF-kappaB, inflammation and cancer.

机构信息

Biotech Research and Innovation Centre, University of Copenhagen, Ole Maaløes Vej 5, Copenhagen DK2200, Denmark.

出版信息

Nat Rev Cancer. 2010 Aug;10(8):561-74. doi: 10.1038/nrc2889.

Abstract

The realization that alterations in inhibitor of apoptosis (IAP) proteins are found in many types of human cancer and are associated with chemoresistance, disease progression and poor prognosis, has sparked a worldwide frenzy in the development of small pharmacological inhibitors of IAPs. The development of such inhibitors has radically changed our knowledge of the signalling processes that are regulated by IAPs. Recent studies indicate that IAPs not only regulate caspases and apoptosis, but also modulate inflammatory signalling and immunity, mitogenic kinase signalling, proliferation and mitosis, as well as cell invasion and metastasis.

摘要

人们认识到凋亡抑制蛋白(IAP)在许多类型的人类癌症中发生改变,并与化疗耐药性、疾病进展和预后不良相关,这激发了全世界开发 IAP 小分子药理学抑制剂的热潮。此类抑制剂的开发极大地改变了我们对 IAP 调控的信号转导过程的认识。最近的研究表明,IAP 不仅调节胱天蛋白酶和细胞凋亡,还调节炎症信号和免疫、有丝分裂原激酶信号、增殖和有丝分裂以及细胞侵袭和转移。

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