子宫内膜样癌前体病变的基因和表观遗传学改变。

IF 5.6 2区 医学 Q1 ONCOLOGY The Journal of Pathology Pub Date : 2024-05-11 DOI:10.1002/path.6278
Osamu Gotoh, Yuko Sugiyama, Akiko Tonooka, Mayuko Kosugi, Sunao Kitaura, Ryu Minegishi, Masatoshi Sano, Sayuri Amino, Rie Furuya, Norio Tanaka, Tomoko Kaneyasu, Kohei Kumegawa, Akiko Abe, Hidetaka Nomura, Yutaka Takazawa, Hiroyuki Kanao, Reo Maruyama, Tetsuo Noda, Seiichi Mori
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引用次数: 0

摘要

增生-癌变序列是子宫内膜癌的一个阶梯式致瘤过程,在这一过程中,正常的子宫内膜上皮会在无抑制雌激素的影响下,通过非典型子宫内膜增生(NAEH)和非典型子宫内膜增生(AEH)而发生癌变。众所周知,NAEH 和 AEH 分别表现为多克隆和单克隆细胞生长;然而,除了局灶性 PTEN 蛋白缺失外,细胞转变过程中发生的遗传和表观遗传学改变在很大程度上仍不为人所知。我们试图探索促进NAEH-AEH转变的潜在分子机制,并确定有助于区分这两种状态的分子标记。我们对 596 个基因(包括 96 个子宫内膜癌驱动基因)的编码外显子进行了靶组测序,并对 48 个 NAEH 和 44 个 AEH 病变进行了 DNA 甲基化组芯片分析,这些病变是分别从 30 个病例的子宫内膜组织中通过宏观或微观切片采集的。测序分析表明,AEH样本中存在PTEN突变和肿瘤细胞的克隆扩增。此外,在整个转变过程中,DNA甲基组的改变表现为启动子/增强子区域和CpG岛的高甲基化,以及与子宫内膜细胞分化和/或肿瘤发生相关的转录因子(包括FOXA2、SOX17和HAND2)DNA结合区域的低甲基化和高甲基化。所确定的区分NAEH和AEH病变的DNA甲基化特征在验证队列中具有可重复性和适度的鉴别能力。这些发现不仅支持了从NAEH到AEH的转变是子宫内膜上皮肿瘤细胞转化过程中的一个重要步骤这一概念,而且还深入揭示了致瘤程序的分子机制。© 2024 作者。病理学杂志》由约翰威利父子有限公司代表大不列颠及爱尔兰病理学会出版。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Genetic and epigenetic alterations in precursor lesions of endometrial endometrioid carcinoma

The hyperplasia–carcinoma sequence is a stepwise tumourigenic programme towards endometrial cancer in which normal endometrial epithelium becomes neoplastic through non-atypical endometrial hyperplasia (NAEH) and atypical endometrial hyperplasia (AEH), under the influence of unopposed oestrogen. NAEH and AEH are known to exhibit polyclonal and monoclonal cell growth, respectively; yet, aside from focal PTEN protein loss, the genetic and epigenetic alterations that occur during the cellular transition remain largely unknown. We sought to explore the potential molecular mechanisms that promote the NAEH–AEH transition and identify molecular markers that could help to differentiate between these two states. We conducted target-panel sequencing on the coding exons of 596 genes, including 96 endometrial cancer driver genes, and DNA methylome microarrays for 48 NAEH and 44 AEH lesions that were separately collected via macro- or micro-dissection from the endometrial tissues of 30 cases. Sequencing analyses revealed acquisition of the PTEN mutation and the clonal expansion of tumour cells in AEH samples. Further, across the transition, alterations to the DNA methylome were characterised by hypermethylation of promoter/enhancer regions and CpG islands, as well as hypo- and hyper-methylation of DNA-binding regions for transcription factors relevant to endometrial cell differentiation and/or tumourigenesis, including FOXA2, SOX17, and HAND2. The identified DNA methylation signature distinguishing NAEH and AEH lesions was reproducible in a validation cohort with modest discriminative capability. These findings not only support the concept that the transition from NAEH to AEH is an essential step within neoplastic cell transformation of endometrial epithelium but also provide deep insight into the molecular mechanism of the tumourigenic programme. © 2024 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

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来源期刊
The Journal of Pathology
The Journal of Pathology 医学-病理学
CiteScore
14.10
自引率
1.40%
发文量
144
审稿时长
3-8 weeks
期刊介绍: The Journal of Pathology aims to serve as a translational bridge between basic biomedical science and clinical medicine with particular emphasis on, but not restricted to, tissue based studies. The main interests of the Journal lie in publishing studies that further our understanding the pathophysiological and pathogenetic mechanisms of human disease. The Journal of Pathology welcomes investigative studies on human tissues, in vitro and in vivo experimental studies, and investigations based on animal models with a clear relevance to human disease, including transgenic systems. As well as original research papers, the Journal seeks to provide rapid publication in a variety of other formats, including editorials, review articles, commentaries and perspectives and other features, both contributed and solicited.
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