Suppr超能文献

PPP6R3-USP6扩增:恶性结节性筋膜炎中的新型致癌机制。

PPP6R3-USP6 amplification: Novel oncogenic mechanism in malignant nodular fasciitis.

作者信息

Guo Ruifeng, Wang Xiaoke, Chou Margaret M, Asmann Yan, Wenger Doris E, Al-Ibraheemi Alyaa, Molavi Diana W, Aboulafia Albert, Jin Long, Fritchie Karen, Oliveira Jennifer L, Jenkins Robert B, Westendorf Jennifer J, Dong Jie, Oliveira Andre M

机构信息

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

Department of Dermatology, Mayo Clinic, Rochester, MN.

出版信息

Genes Chromosomes Cancer. 2016 Aug;55(8):640-9. doi: 10.1002/gcc.22366. Epub 2016 May 30.

Abstract

Nodular fasciitis (NF) is a clonal self-limited neoplastic proliferation characterized by rearrangements of the USP6 locus in most examples. To our knowledge well-documented malignant behavior has never been previously observed in NF. In this report we present an unusual case of NF with classical histologic features that showed a protracted clinical course characterized by multiple recurrences and eventual metastatic behavior over a period of 10 years. Molecular analyses revealed the presence and amplification of the novel PPPR6-USP6 gene fusion, which resulted in USP6 mRNA transcriptional upregulation. These findings further support the oncogenic role of the USP6 protease in mesenchymal neoplasia and expand the biologic potential of NF. © 2016 Wiley Periodicals, Inc.

摘要

结节性筋膜炎(NF)是一种克隆性自限性肿瘤性增殖,在大多数病例中其特征为USP6基因座重排。据我们所知,此前从未在NF中观察到有充分记录的恶性行为。在本报告中,我们呈现了一例具有典型组织学特征的不寻常NF病例,该病例显示出长达10年的迁延临床病程,其特点是多次复发并最终出现转移行为。分子分析揭示了新型PPPR6-USP6基因融合的存在及扩增,这导致USP6 mRNA转录上调。这些发现进一步支持了USP6蛋白酶在间叶性肿瘤形成中的致癌作用,并扩展了NF的生物学潜能。© 2016威利期刊公司

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验