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雄激素类固醇驱动的猪卵巢类干细胞的调控有利于其肿瘤转化的发生。

Anabolic Steroids-Driven Regulation of Porcine Ovarian Putative Stem Cells Favors the Onset of Their Neoplastic Transformation.

机构信息

Department of Endocrinology, Faculty of Biology, Institute of Zoology and Biomedical Research, Jagiellonian University in Krakow, Gronostajowa 9 Street, 30-387 Krakow, Poland.

Department of Histology, Faculty of Medicine, Jagiellonian University Medical College, Kopernika 7 Street, 31-034 Krakow, Poland.

出版信息

Int J Mol Sci. 2021 Oct 30;22(21):11800. doi: 10.3390/ijms222111800.

Abstract

Nandrolone (Ndn) and boldenone (Bdn), the synthetic testosterone analogues with strong anabolic effects, despite being recognized as potentially carcinogenic compounds, are commonly abused by athletes and bodybuilders, which includes women, worldwide. This study tested the hypothesis that different doses of Ndn and Bdn can initiate neoplastic transformation of porcine ovarian putative stem cells (poPSCs). Immunomagnetically isolated poPSCs were expanded ex vivo in the presence of Ndn or Bdn, for 7 and 14 days. Results show that pharmacological doses of both Ndn and Bdn, already after 7 days of poPSCs culture, caused a significant increase of selected, stemness-related markers of cancer cells: CD44 and CD133. Notably, Ndn also negatively affected poPSCs growth not only by suppressing their proliferation and mitochondrial respiration but also by inducing apoptosis. This observation shows, for the first time, that chronic exposure to Ndn or Bdn represents a precondition that might enhance risk of poPSCs neoplastic transformation. These studies carried out to accomplish detailed molecular characterization of the ex vivo expanded poPSCs and their potentially cancerous derivatives (PCDs) might be helpful to determine their suitability as nuclear donor cells (NDCs) for further investigations focused on cloning by somatic cell nuclear transfer (SCNT). Such investigations might also be indispensable to estimate the capabilities of nuclear genomes inherited from poPSCs and their PCDs to be epigenetically reprogrammed (dedifferentiated) in cloned pig embryos generated by SCNT. This might open up new possibilities for biomedical research aimed at more comprehensively recognizing genetic and epigenetic mechanisms underlying not only tumorigenesis but also reversal/retardation of pro-tumorigenic intracellular events.

摘要

去氢睪酮(Ndn)和宝丹酮(Bdn)是具有强烈合成代谢作用的合成睪酮类似物,尽管被认为是潜在的致癌化合物,但仍被全世界的运动员和健美运动员滥用,包括女性。本研究检验了以下假设,即不同剂量的 Ndn 和 Bdn 可引发猪卵巢类原始干细胞(poPSCs)的肿瘤转化。使用免疫磁珠分离的 poPSCs 在 Ndn 或 Bdn 的存在下进行体外扩增,时间分别为 7 天和 14 天。结果表明,药理学剂量的 Ndn 和 Bdn 在培养 poPSCs7 天后,即可显著增加与癌细胞干性相关的特定标志物:CD44 和 CD133。值得注意的是,Ndn 不仅通过抑制细胞增殖和线粒体呼吸,还通过诱导细胞凋亡来抑制 poPSCs 的生长。这一观察结果首次表明,慢性暴露于 Ndn 或 Bdn 可能会增加 poPSCs 肿瘤转化的风险。这些研究旨在对体外扩增的 poPSCs 及其潜在的癌细胞衍生物(PCDs)进行详细的分子特征分析,这可能有助于确定它们作为核供体细胞(NDCs)的适用性,以便进一步进行集中于体细胞核转移(SCNT)的克隆研究。这些研究对于评估从 poPSCs 和其 PCDs 遗传的核基因组在通过 SCNT 产生的克隆猪胚胎中被重新编程(去分化)的能力也是必不可少的,这可能为旨在更全面地认识肿瘤发生以及肿瘤发生前细胞内事件的逆转/延缓的遗传和表观遗传机制的生物医学研究开辟新的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f8c/8583785/90d91f93f3e3/ijms-22-11800-g001.jpg

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