Suppr超能文献

过氧化物酶体增殖物激活受体γ配体的抗白血病作用。

Anti-leukemic effects of PPARγ ligands.

机构信息

Gyeongsang National University Hospital, Gyeongsang National University School of Medicine, Jinju, South Korea.

Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.

出版信息

Cancer Lett. 2018 Apr 1;418:10-19. doi: 10.1016/j.canlet.2018.01.020. Epub 2018 Jan 11.

Abstract

The peroxisome proliferator-activated receptor (PPAR) γ, a subtype of PPARs, is a member of the nuclear receptor family. PPARγ and its ligands contribute to various types of diseases including cancer. Given that currently developed therapies against leukemia are not very effective or safe, PPARγ ligands have been shown to be a new class of compounds with the potential to treat hematologic malignancies, particularly leukemia. The capability of PPARγ ligands to induce apoptosis, inhibit proliferation, and promote differentiation of leukemia cells suggests it has significant potential as a drug against leukemia. However, the specific mechanisms and molecules involved are not well-understood, although a number of PPARγ ligands with anti-leukemic effects have been identified. This may explain why PPARγ ligands have not been widely evaluated in clinical trials. To fill the gaps in the lack of understanding of specific anti-leukemic processes of PPARγ ligands and further adapt these molecules as anti-leukemic agents, this review describes previous studies of the anti-leukemic effects of PPARγ ligands.

摘要

过氧化物酶体增殖物激活受体 (PPAR)γ 是 PPAR 亚型之一,是核受体家族的成员。PPARγ 及其配体与多种疾病有关,包括癌症。鉴于目前针对白血病的治疗方法不是非常有效或安全,PPARγ 配体已被证明是一类具有治疗血液恶性肿瘤(尤其是白血病)潜力的新型化合物。PPARγ 配体诱导白血病细胞凋亡、抑制增殖和促进分化的能力表明,它具有作为白血病药物的巨大潜力。然而,涉及的具体机制和分子尚不清楚,尽管已经确定了一些具有抗白血病作用的 PPARγ 配体。这可能解释了为什么 PPARγ 配体尚未在临床试验中广泛评估。为了填补对 PPARγ 配体特定抗白血病过程缺乏了解的空白,并进一步将这些分子作为抗白血病药物,本综述描述了之前关于 PPARγ 配体抗白血病作用的研究。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验