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USP6 诱导性肿瘤:动脉瘤样骨囊肿和结节性筋膜炎的生物学谱。

USP6-induced neoplasms: the biologic spectrum of aneurysmal bone cyst and nodular fasciitis.

机构信息

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA; Department of Orthopedics, Mayo Clinic, Rochester, MN, USA.

出版信息

Hum Pathol. 2014 Jan;45(1):1-11. doi: 10.1016/j.humpath.2013.03.005. Epub 2013 Jun 12.

Abstract

USP6 (also known as TRE17) is a ubiquitin-specific protease that was identified as an oncogene in transfection experiments with Ewing sarcoma DNA 2 decades ago. Until recently, little was known about USP6 function and mechanisms of oncogenic activation. The identification of USP6 fusion genes in aneurysmal bone cyst (ABC) and, more recently, in nodular fasciitis led to a better understanding of the pathogenesis of these lesions. Furthermore, the detection of USP6 genomic rearrangements or USP6 fusion genes may be used as a diagnostic tool for these lesions. In this review, we discuss the clinicopathologic features, molecular pathology, and pathogenesis of ABC and nodular fasciitis. We also discuss the possible line of differentiation of ABC and its relationship to nodular fasciitis and other lesions.

摘要

USP6(也称为 TRE17)是一种泛素特异性蛋白酶,在 20 年前用尤文肉瘤 DNA 进行转染实验时被鉴定为致癌基因。直到最近,人们对 USP6 的功能及其致癌激活机制知之甚少。在动脉瘤样骨囊肿(ABC)中发现 USP6 融合基因,最近在结节性筋膜炎中也发现了 USP6 融合基因,这使人们对这些病变的发病机制有了更好的理解。此外,检测 USP6 基因组重排或 USP6 融合基因可用作这些病变的诊断工具。在这篇综述中,我们讨论了 ABC 和结节性筋膜炎的临床病理特征、分子病理学和发病机制。我们还讨论了 ABC 的可能分化途径及其与结节性筋膜炎和其他病变的关系。

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