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Androgen Receptor Roles in Insulin Resistance and Obesity in Males: The Linkage of Androgen-Deprivation Therapy to Metabolic Syndrome

机译:雄激素受体在男性胰岛素抵抗和肥胖中的作用:雄激素剥夺疗法与代谢综合征的联系

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摘要

Prostate cancer (PCa) is one of the most frequently diagnosed malignancies in men. Androgen-deprivation therapy (ADT) is the first-line treatment and fundamental management for men with advanced PCa to suppress functions of androgen/androgen receptor (AR) signaling. ADT is effective at improving cancer symptoms and prolonging survival. However, epidemiologi-cal and clinical studies support the notion that testosterone deficiency in men leads to the development of metabolic syndrome that increases cardiovascular disease risk. The underlying mechanisms by which androgen/AR signaling regulates metabolic ho-meostasis in men are complex, and in this review, we discuss molecular mechanisms mediated by AR signaling that link ADT to metabolic syndrome. Results derived from various AR knockout mouse models reveal tissue-specific AR signaling that is involved in regulation of metabolism. These data suggest that steps be taken early to manage metabolic complications associated with PCa patients receiving ADT, which could be accomplished using tissue-selective modulation of AR signaling and by treatment with insulin-sensitizing agents.
机译:前列腺癌(PCa)是男性中最常被诊断出的恶性肿瘤之一。雄激素剥夺疗法(ADT)是患有晚期PCa的男性的一线治疗和基础治疗,可抑制雄激素/雄激素受体(AR)信号传导功能。 ADT可有效改善癌症症状并延长生存期。然而,流行病学和临床研究支持以下观念:男性睾丸激素缺乏会导致代谢综合征的发展,从而增加心血管疾病的风险。雄激素/ AR信号调节男性代谢ho-稳态的潜在机制是复杂的,在本综述中,我们讨论了由AR信号介导的将ADT与代谢综合症联系起来的分子机制。从各种AR基因敲除小鼠模型得出的结果表明,组织特异性AR信号传导参与代谢的调节。这些数据表明,应尽早采取措施来管理与接受ADT的PCa患者相关的代谢并发症,这可以通过AR信号的组织选择性调节和胰岛素增敏剂的治疗来完成。

著录项

  • 来源
    《Diabetes》 |2014年第10期|3180-3188|共9页
  • 作者单位

    Department of Pathology, George Whipple Laboratory for Cancer Research,University of Rochester Medical Center, Rochester, NY,Department of Urology, George Whipple Laboratory for Cancer Research, University of Rochester Medical Center, Rochester, NY,Wilmot Cancer Center, University of Rochester Medical Center, Rochester, NY;

    Department of Pathology, George Whipple Laboratory for Cancer Research,University of Rochester Medical Center, Rochester, NY,Department of Urology, George Whipple Laboratory for Cancer Research, University of Rochester Medical Center, Rochester, NY,Wilmot Cancer Center, University of Rochester Medical Center, Rochester, NY;

    Department of Pathology, George Whipple Laboratory for Cancer Research,University of Rochester Medical Center, Rochester, NY,Department of Urology, George Whipple Laboratory for Cancer Research, University of Rochester Medical Center, Rochester, NY,Wilmot Cancer Center, University of Rochester Medical Center, Rochester, NY;

    Department of Pathology, George Whipple Laboratory for Cancer Research,University of Rochester Medical Center, Rochester, NY,Department of Urology, George Whipple Laboratory for Cancer Research, University of Rochester Medical Center, Rochester, NY,Wilmot Cancer Center, University of Rochester Medical Center, Rochester, NY;

    Department of Pathology, George Whipple Laboratory for Cancer Research,University of Rochester Medical Center, Rochester, NY,Department of Urology, George Whipple Laboratory for Cancer Research, University of Rochester Medical Center, Rochester, NY,Wilmot Cancer Center, University of Rochester Medical Center, Rochester, NY,Sex Hormone Research Center, China Medical University/Hospital, Taichung, Taiwan;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:46:21

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