BCL6, a key oncogene, in the placenta, pre-eclampsia and endometriosis

IF 14.8 1区 医学 Q1 OBSTETRICS & GYNECOLOGY
F. Louwen, N. Kreis, A. Ritter, A. Friemel, C. Solbach, Juping Yuan
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引用次数: 5

Abstract

Abstract BACKGROUND The key oncogene B-cell lymphoma 6 (BCL6) drives malignant progression by promoting proliferation, overriding DNA damage checkpoints and blocking cell terminal differentiation. However, its functions in the placenta and the endometrium remain to be defined. OBJECTIVE AND RATIONALE Recent studies provide evidence that BCL6 may play various roles in the human placenta and the endometrium. Deregulated BCL6 might be related to the pathogenesis of pre-eclampsia (PE) as well as endometriosis. In this narrative review, we aimed to summarize the current knowledge regarding the pathophysiological role of BCL6 in these two reproductive organs, discuss related molecular mechanisms, and underline associated research perspectives. SEARCH METHODS We conducted a comprehensive literature search using PubMed for human, animal and cellular studies published until October 2021 in the following areas: BCL6 in the placenta, in PE and in endometriosis, in combination with its functions in proliferation, fusion, migration, invasion, differentiation, stem/progenitor cell maintenance and lineage commitment. OUTCOMES The data demonstrate that BCL6 is important in cell proliferation, survival, differentiation, migration and invasion of trophoblastic cells. BCL6 may have critical roles in stem/progenitor cell survival and differentiation in the placenta and the endometrium. BCL6 is aberrantly upregulated in pre-eclamptic placentas and endometriotic lesions through various mechanisms, including changes in gene transcription and mRNA translation as well as post-transcriptional/translational modifications. Importantly, increased endometrial BCL6 is considered to be a non-invasive diagnostic marker for endometriosis and a predictor for poor outcomes of IVF. These data highlight that BCL6 is crucial for placental development and endometrium homeostasis, and its upregulation is associated with the pathogenesis of PE, endometriosis and infertility. WIDER IMPLICATIONS The lesson learned from studies of the key oncogene BCL6 reinforces the notion that numerous signaling pathways and regulators are shared by tumors and reproductive organs. Their alteration may promote the progression of malignancies as well as the development of gestational and reproductive disorders.
BCL6是胎盘、子痫前期和子宫内膜异位症的关键致癌基因
摘要背景关键癌基因B细胞淋巴瘤6(BCL6)通过促进增殖、克服DNA损伤检查点和阻断细胞末端分化来驱动恶性进展。然而,它在胎盘和子宫内膜中的功能仍有待确定。目的与原理最近的研究证明BCL6可能在人类胎盘和子宫内膜中发挥多种作用。BCL6的下调可能与子痫前期(PE)和子宫内膜异位症的发病机制有关。在这篇叙述性综述中,我们旨在总结目前关于BCL6在这两个生殖器官中的病理生理作用的知识,讨论相关的分子机制,并强调相关的研究前景。检索方法我们使用PubMed对截至2021年10月发表的以下领域的人类、动物和细胞研究进行了全面的文献检索:胎盘、PE和子宫内膜异位症中的BCL6及其在增殖、融合、迁移、侵袭、分化、干/祖细胞维持和谱系承诺中的功能。结果表明BCL6在滋养层细胞的增殖、存活、分化、迁移和侵袭中具有重要作用。BCL6可能在胎盘和子宫内膜的干/祖细胞存活和分化中发挥关键作用。BCL6在先兆子痫胎盘和子宫内膜异位病变中通过各种机制异常上调,包括基因转录和mRNA翻译的变化以及转录后/翻译修饰。重要的是,子宫内膜BCL6的增加被认为是子宫内膜异位症的非侵入性诊断标志物,也是IVF不良结果的预测因素。这些数据强调,BCL6对胎盘发育和子宫内膜稳态至关重要,其上调与PE、子宫内膜异位症和不孕的发病机制有关。更广泛的意义从关键癌基因BCL6的研究中吸取的教训强化了肿瘤和生殖器官共享许多信号通路和调节因子的概念。它们的改变可能促进恶性肿瘤的进展以及妊娠和生殖疾病的发展。
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来源期刊
Human Reproduction Update
Human Reproduction Update 医学-妇产科学
CiteScore
28.80
自引率
1.50%
发文量
38
期刊介绍: Human Reproduction Update is the leading journal in its field, boasting a Journal Impact FactorTM of 13.3 and ranked first in Obstetrics & Gynecology and Reproductive Biology (Source: Journal Citation ReportsTM from Clarivate, 2023). It specializes in publishing comprehensive and systematic review articles covering various aspects of human reproductive physiology and medicine. The journal prioritizes basic, transitional, and clinical topics related to reproduction, encompassing areas such as andrology, embryology, infertility, gynaecology, pregnancy, reproductive endocrinology, reproductive epidemiology, reproductive genetics, reproductive immunology, and reproductive oncology. Human Reproduction Update is published on behalf of the European Society of Human Reproduction and Embryology (ESHRE), maintaining the highest scientific and editorial standards.
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