分解 p53 的代谢活性和肿瘤抑制活性。

IF 11.4 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Yoshitaka Sakurai, Naoto Kubota, Takashi Kadowaki
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引用次数: 0

摘要

肿瘤抑制因子 p53 可调节代谢平衡。最近,Tsaousidou 等人报告说,尽管存在肥胖和胰岛素抵抗,但通过下调 Tudor 交互修复调节因子(TIRR)选择性地激活 p53,可获得抗癌保护,这为了解 p53 在肿瘤发生和系统代谢交汇处的作用提供了新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dissociating the metabolic and tumor-suppressive activity of p53.

The tumor suppressor p53 regulates metabolic homeostasis. Recently, Tsaousidou et al. reported that selective activation of p53 via downregulation of Tudor interacting repair regulator (TIRR) confers protection against cancer despite obesity and insulin resistance, providing new insights into the role of p53 at the intersection of oncogenesis and systemic metabolism.

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来源期刊
Trends in Endocrinology and Metabolism
Trends in Endocrinology and Metabolism 医学-内分泌学与代谢
CiteScore
20.10
自引率
0.00%
发文量
98
审稿时长
82 days
期刊介绍: Trends in Endocrinology and Metabolism (TEM) stands as a premier Reviews journal in the realms of metabolism and endocrinology. Our commitment is reflected in the publication of refined, concise, and highly impactful articles that delve into cutting-edge topics, encompassing basic, translational, and clinical aspects. From state-of-the-art treatments for endocrine diseases to groundbreaking developments in molecular biology, TEM provides comprehensive coverage. Explore recent advancements in diabetes, endocrine diseases, obesity, neuroendocrinology, immunometabolism, molecular and cellular biology, and a myriad of other areas through our journal. TEM serves as an invaluable resource for researchers, clinicians, lecturers, teachers, and students. Each monthly issue is anchored by Reviews and Opinion articles, with Reviews meticulously chronicling recent and significant developments, often contributed by leading researchers in specific fields. Opinion articles foster debate and hypotheses. Our shorter pieces include Science & Society, shedding light on issues at the intersection of science, society, and policy; Spotlights, which focus on exciting recent developments in the literature, and single-point hypotheses as Forum articles. We wholeheartedly welcome and encourage responses to previously published TEM content in the form of Letters.
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