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塔斯帕酶1:一种充满诸多生物学惊喜的蛋白酶。

Taspase 1: A protease with many biological surprises.

作者信息

Niizuma Hidetaka, Cheng Emily H, Hsieh James J

机构信息

Human Oncology & Pathogenesis Program; Memorial Sloan-Kettering Cancer Center; New York, NY, USA; Department of Pediatrics; Tohoku University Graduate School of Medicine; Sendai, Miyagi, Japan.

Human Oncology & Pathogenesis Program; Memorial Sloan-Kettering Cancer Center; New York, NY, USA; Department of Pathology; Memorial Sloan-Kettering Cancer Center; New York, NY, USA.

出版信息

Mol Cell Oncol. 2015 Jan 23;2(4):e999513. doi: 10.1080/23723556.2014.999513. eCollection 2015 Oct-Dec.

Abstract

Taspase 1 (TASP1) cleaves the mixed-lineage leukemia (MLL) and transcription factor (TF) IIA families of nuclear proteins to orchestrate various biological processes. TASP1 is not a classical oncogene, but assists in cell proliferation and permits oncogenic initiation through cleavage of MLL and TFIIA. TASP1 is thus better classified as a "non-oncogene addiction" protease, and targeting TASP1 offers a novel and attractive anticancer therapeutic strategy.

摘要

塔斯帕酶1(TASP1)可切割核蛋白的混合谱系白血病(MLL)和转录因子(TF)IIA家族,以协调各种生物学过程。TASP1不是经典的癌基因,但通过切割MLL和TFIIA来协助细胞增殖并促进致癌起始。因此,TASP1更适合归类为“非癌基因成瘾”蛋白酶,靶向TASP1提供了一种新颖且有吸引力的抗癌治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1712/4905357/101171b53f40/kmco-02-04-999513-g001.jpg

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