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患有性别决定缺陷和生殖细胞癌个体的基因组不稳定性。

Genomic instability in individuals with sex determination defects and germ cell cancer.

作者信息

Krivega Maria, Zimmer Jutta, Slezko Anna, Frank-Herrmann Petra, Rehnitz Julia, Hohenfellner Markus, Bettendorf Markus, Luzarowski Marcin, Strowitzki Thomas

机构信息

Research Group of Gonadal Differentiation and Embryonic Development, Department of Gynecological Endocrinology & Fertility Disorders, Women Hospital, University of Heidelberg, 69120, Heidelberg, Germany.

Department of Gynecological Endocrinology & Fertility Disorders, Women Hospital, University of Heidelberg, 69120, Heidelberg, Germany.

出版信息

Cell Death Discov. 2023 May 23;9(1):173. doi: 10.1038/s41420-023-01470-6.

Abstract

The ability to transmit genetic information through generations depends on the preservation of genome integrity. Genetic abnormalities affect cell differentiation, causing tissue specification defects and cancer. We addressed genomic instability in individuals with Differences of Sex Development (DSD), characterized by gonadal dysgenesis, infertility, high susceptibility for different types of cancer, especially Germ Cell Tumors (GCT), and in men with testicular GCTs. Whole proteome analysis of leukocytes, supported by specific gene expression assessment, and dysgenic gonads characterization, uncovered DNA damage phenotypes with altered innate immune response and autophagy. Further examination of DNA damage response revealed a reliance on deltaTP53, which was compromised by mutations in the transactivation domain in DSD-individuals with GCT. Accordingly, drug-induced rescue of DNA damage was achieved by autophagy inhibition but not by stabilization of TP53 in DSD-individuals' blood in vitro. This study elucidates possibilities for prophylactic treatments of DSD-individuals, as well as new diagnostic approaches of GCT.

摘要

遗传信息跨代传递的能力取决于基因组完整性的维持。基因异常会影响细胞分化,导致组织特异性缺陷和癌症。我们研究了性发育差异(DSD)个体以及睾丸生殖细胞肿瘤(GCT)男性患者的基因组不稳定性,DSD个体的特征为性腺发育不全、不育、对不同类型癌症尤其是生殖细胞肿瘤(GCT)的高易感性。通过特定基因表达评估和发育异常性腺特征分析支持的白细胞全蛋白质组分析,发现了具有改变的先天免疫反应和自噬的DNA损伤表型。对DNA损伤反应的进一步研究揭示了对δTP53的依赖,而在患有GCT的DSD个体中,反式激活域的突变损害了这种依赖。因此,在体外,通过自噬抑制而非TP53的稳定来实现对DSD个体血液中DNA损伤的药物诱导挽救。这项研究阐明了DSD个体预防性治疗的可能性以及GCT的新诊断方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7692/10202957/0c4863223976/41420_2023_1470_Fig1_HTML.jpg

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