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简明综述:雄激素受体在包括前列腺、胚胎、基质和造血谱系在内的干细胞/祖细胞中的不同作用。

Concise review: androgen receptor differential roles in stem/progenitor cells including prostate, embryonic, stromal, and hematopoietic lineages.

机构信息

Departments of Pathology, Urology, Radiation Oncology, the George Whipple Lab for Cancer Research, and The Wilmot Cancer Center, University of Rochester Medical Center, Rochester, New York, USA.

出版信息

Stem Cells. 2014 Sep;32(9):2299-308. doi: 10.1002/stem.1722.

Abstract

Stem/progenitor (S/P) cells are special types of cells that have the ability to generate tissues throughout their entire lifetime and play key roles in the developmental process. Androgen and the androgen receptor (AR) signals are the critical determinants in male gender development, suggesting that androgen and AR signals might modulate the behavior of S/P cells. In this review, we summarize the AR effects on the behavior of S/P cells, including self-renewal, proliferation, apoptosis, and differentiation in normal S/P cells, as well as proliferation, invasion, and self-renewal in prostate cancer S/P cells. AR plays a protective role in the oxidative stress-induced apoptosis in embryonic stem cells. AR inhibits the self-renewal of embryonic stem cells, bone marrow stromal cells, and prostate S/P cells, but promotes their differentiation except for adipogenesis. However, AR promotes the proliferation of hematopoietic S/P cells and stimulates hematopoietic lineage differentiation. In prostate cancer S/P cells, AR suppresses their self-renewal, metastasis, and invasion. Together, AR differentially influences the characteristics of normal S/P cells and prostate cancer S/P cells, and targeting AR might improve S/P cell transplantation therapy, especially in embryonic stem cells and bone marrow stromal cells.

摘要

干细胞/祖细胞(S/P)是具有在整个生命周期中产生组织的能力的特殊类型的细胞,并且在发育过程中发挥关键作用。雄激素和雄激素受体(AR)信号是男性性别发育的关键决定因素,这表明雄激素和 AR 信号可能调节 S/P 细胞的行为。在这篇综述中,我们总结了 AR 对 S/P 细胞行为的影响,包括正常 S/P 细胞中的自我更新、增殖、凋亡和分化,以及前列腺癌 S/P 细胞中的增殖、侵袭和自我更新。AR 在胚胎干细胞的氧化应激诱导凋亡中起保护作用。AR 抑制胚胎干细胞、骨髓基质细胞和前列腺 S/P 细胞的自我更新,但促进其分化,除了脂肪生成。然而,AR 促进造血 S/P 细胞的增殖并刺激造血谱系分化。在前列腺癌 S/P 细胞中,AR 抑制其自我更新、转移和侵袭。总之,AR 对正常 S/P 细胞和前列腺癌 S/P 细胞的特征有不同的影响,靶向 AR 可能改善 S/P 细胞移植治疗,特别是在胚胎干细胞和骨髓基质细胞中。

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