DAZ基因缺失与睾丸生殖细胞肿瘤发生和不育有关:来自人胚胎干细胞种系分化的证据。

IF 2.9 3区 医学 Q2 ONCOLOGY
American journal of cancer research Pub Date : 2025-09-25 eCollection Date: 2025-01-01 DOI:10.62347/NDPD8973
Junqing Chen, Chuyu Li, Shuangshuang Qiu, Wenrui Zhu, Xi He, Dawei Gao, Zifeng Chen, Xingli Tong, Feiyang Diao
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引用次数: 0

摘要

y染色体AZFc缺陷,包括DAZ基因家族,是严重男性不育最常见的遗传原因之一。流行病学和分子证据表明生殖细胞发育异常与睾丸生殖细胞肿瘤(TGCT)之间存在发育联系,但DAZ缺乏是否以及如何与TGCT易感性相关仍不清楚。利用特定的人胚胎干细胞(hESC)模型,我们构建了一株daz缺失细胞系(SKLRMe001-A)并对其进行了表征,并将其诱导为人原始生殖细胞样细胞(hpgclc)的效率与H1对照细胞系进行了比较。我们评估了胚胎样网络和HMGA1-P53-MAPK/PI3K通路之间的交集,以探索DAZ缺陷和TGCT易感性之间的潜在联系。DAZ缺乏显著降低了hPGCLC的诱导效率,下调了SOX17、BLIMP1和TFAP2C等早期谱系标记,并伴有s期缩短、细胞周期失调和凋亡增加。RNA测序和富集分析表明,HMGA1持续上调,并指出P53应激反应和PI3K/AKT和MAPK信号轴的稳态失调。这些发现与TGCT的特征一致,包括维持胚胎样程序、激活增殖信号和增强DNA损伤反应。因此,我们认为DAZ缺乏导致的谱系分化缺陷和应激与生存信号之间的不匹配可能在体内产生“未分化易感”细胞群,增加TGCT的风险,同时也解释了男性不育的发育基础。利用人类体外模型,本研究将DAZ缺陷与不孕症和TGCT易感性联系起来,并确定HMGA1是中心转录信号枢纽。这一发现为DAZ缺乏人群的风险分层和早期监测提供了分子线索,并提示针对HMGA1、PI3K/AKT和MAPK通路的干预可能同时改善种系分化和降低潜在的肿瘤风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Deficiency of DAZ genes links testicular germ cell tumorigenesis and infertility: evidence from human embryonic stem cell germline differentiation.

Y-chromosome AZFc deficiency, which includes the DAZ gene family, is one of the most common genetic causes of severe male infertility. Epidemiological and molecular evidence suggest a developmental link between abnormalities in germ cell development and testicular germ cell tumor (TGCT), but whether and how DAZ deficiency is associated with TGCT susceptibility remains unclear. Using a specific human embryonic stem cell (hESC) model, we constructed and characterized a DAZ-deleted cell line (SKLRMe001-A) and compared its efficiency of induction into human primordial germ cell-like cells (hPGCLCs) with that of the H1 control line. We assessed intersections between embryonic-like networks and HMGA1-P53-MAPK/PI3K pathways to explore the potential connection between DAZ deficiency and TGCT susceptibility. DAZ deficiency significantly reduced hPGCLC induction efficiency and downregulated early lineage markers such as SOX17, BLIMP1, and TFAP2C, accompanied by S-phase shortening, cell cycle dysregulation, and increased apoptosis. RNA sequencing and enrichment analyses indicated sustained upregulation of HMGA1 and pointed to dysregulated homeostasis of P53 stress responses and PI3K/AKT and MAPK signaling axes. These findings are consistent with features of TGCT, including maintenance of embryonic-like programs, activation of proliferative signals, and heightened DNA damage responses. Therefore, we propose that lineage differentiation defects and mismatches between stress and survival signaling caused by DAZ deficiency may produce in vivo a population of "undifferentiated and susceptible" cells that increase the risk of TGCT, while also explaining the developmental basis of male infertility. Using a human in vitro model, this study links DAZ deficiency to both infertility and TGCT susceptibility and identifies HMGA1 as a central transcriptional-signaling hub. This finding provides molecular clues for risk stratification and early surveillance in populations with DAZ deficiency and suggests that interventions targeting HMGA1 and the PI3K/AKT and MAPK pathways may simultaneously improve germline differentiation and reduce potential tumor risk.

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来源期刊
自引率
3.80%
发文量
263
期刊介绍: The American Journal of Cancer Research (AJCR) (ISSN 2156-6976), is an independent open access, online only journal to facilitate rapid dissemination of novel discoveries in basic science and treatment of cancer. It was founded by a group of scientists for cancer research and clinical academic oncologists from around the world, who are devoted to the promotion and advancement of our understanding of the cancer and its treatment. The scope of AJCR is intended to encompass that of multi-disciplinary researchers from any scientific discipline where the primary focus of the research is to increase and integrate knowledge about etiology and molecular mechanisms of carcinogenesis with the ultimate aim of advancing the cure and prevention of this increasingly devastating disease. To achieve these aims AJCR will publish review articles, original articles and new techniques in cancer research and therapy. It will also publish hypothesis, case reports and letter to the editor. Unlike most other open access online journals, AJCR will keep most of the traditional features of paper print that we are all familiar with, such as continuous volume, issue numbers, as well as continuous page numbers to retain our comfortable familiarity towards an academic journal.
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