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Merkel 细胞癌的奇特案例:表观遗传年轻化和缺乏多能性。

The curious case of Merkel cell carcinoma: epigenetic youth and lack of pluripotency.

机构信息

Department of Pathology, GROW-School for Oncology & Developmental Biology, Maastricht University, Medical Centre+ , Maastricht, The Netherlands.

Institute for Biomedical Engineering, Department of Cell Biology, RWTH Aachen, University Hospital , Aachen, Germany.

出版信息

Epigenetics. 2020 Dec;15(12):1319-1324. doi: 10.1080/15592294.2020.1773096. Epub 2020 May 30.

Abstract

Merkel cell carcinoma (MCC) is a very rare, but highly aggressive skin cancer which occurs mainly in elderly patients. MCC cells show an expression pattern of three cell lineages: epithelial, neuroendocrine, and B-cell progenitor. This trilinear expression pattern suggests stemness activity in MCC. The etiopathogenesis of MCC is either linked to the Merkel cell polyomavirus (MCPyV) or in a smaller proportion (20%) to high levels of UV-induced somatic mutations. Both viral presence and accumulation of mutations have been shown to be associated with accelerated DNA methylation Age (DNAmAge) compared to chronological age. The MCC DNAmAge was significantly lower compared to the chronological age, which was irrespective of the viral presence or mutational burden. Although these features indicate some aspects of stemness in MCC cells, gene-expression-based pluripotency testing did not provide evidence for pluripotency of MCC cells.

摘要

默克尔细胞癌(Merkel cell carcinoma,MCC)是一种非常罕见但侵袭性很强的皮肤癌,主要发生在老年患者中。MCC 细胞表现出三种细胞谱系的表达模式:上皮、神经内分泌和 B 细胞祖细胞。这种三线表达模式提示 MCC 具有干性活动。MCC 的病因学要么与 Merkel 细胞多瘤病毒(Merkel cell polyomavirus,MCPyV)有关,要么在较小比例(20%)与高水平的紫外线诱导的体细胞突变有关。病毒的存在和突变的积累都与与实际年龄相比加速的 DNA 甲基化年龄(DNAmAge)有关。与实际年龄相比,MCC 的 DNAmAge 明显较低,而与病毒的存在或突变负担无关。尽管这些特征表明 MCC 细胞具有一些干性方面,但基于基因表达的多能性测试并未提供 MCC 细胞多能性的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af13/7678933/09a9f99b9209/KEPI_A_1773096_F0001_C.jpg

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