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解析上皮样血管内皮瘤的生物学特性,一种由TAZ-CAMTA1融合驱动的肉瘤。

Unraveling the Biology of Epithelioid Hemangioendothelioma, a TAZ-CAMTA1 Fusion Driven Sarcoma.

作者信息

Seavey Caleb N, Pobbati Ajaybabu V, Rubin Brian P

机构信息

Department of Cancer Biology, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH 44195, USA.

Department of General Surgery, Digestive Disease and Surgery Institute, Cleveland Clinic Foundation, Cleveland, OH 44195, USA.

出版信息

Cancers (Basel). 2022 Jun 16;14(12):2980. doi: 10.3390/cancers14122980.

Abstract

The activities of YAP and TAZ, the end effectors of the Hippo pathway, are consistently altered in cancer, and this dysregulation drives aggressive tumor phenotypes. While the actions of these two proteins aid in tumorigenesis in the majority of cancers, the dysregulation of these proteins is rarely sufficient for initial tumor development. Herein, we present a unique TAZ-driven cancer, epithelioid hemangioendothelioma (EHE), which harbors a gene fusion in at least 90% of cases. Recent investigations have elucidated the mechanisms by which YAP/TAP-fusion oncoproteins function and drive tumorigenesis. This review presents a critical evaluation of this recent work, with a particular focus on how the oncoproteins alter the normal activity of TAZ and YAP, and, concurrently, we generate a framework for how we can target the gene fusions in patients. Since EHE represents a paradigm of YAP/TAZ dysregulation in cancer, targeted therapies for EHE may also be effective against other YAP/TAZ-dependent cancers.

摘要

Hippo信号通路的终末效应分子YAP和TAZ的活性在癌症中持续发生改变,这种失调驱动了侵袭性肿瘤表型。虽然这两种蛋白的作用在大多数癌症的肿瘤发生过程中发挥作用,但这些蛋白的失调很少足以引发初始肿瘤发展。在此,我们介绍一种独特的由TAZ驱动的癌症——上皮样血管内皮瘤(EHE),在至少90%的病例中存在基因融合。最近的研究阐明了YAP/TAP融合癌蛋白发挥功能并驱动肿瘤发生的机制。本综述对这项最新研究进行了批判性评估,特别关注癌蛋白如何改变TAZ和YAP的正常活性,同时,我们构建了一个针对患者基因融合的靶向治疗框架。由于EHE代表了癌症中YAP/TAZ失调的范例,针对EHE的靶向治疗可能对其他YAP/TAZ依赖性癌症也有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3933/9221450/030f19994b22/cancers-14-02980-g001.jpg

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