PPAR受体和配体在血液恶性肿瘤发病和治疗中的作用

IF 0.9 Q4 HEMATOLOGY Hemato Pub Date : 2022-06-30 DOI:10.3390/hemato3030029
J Wu, M. Zhang, Allison Faircloth
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引用次数: 0

摘要

过氧化物酶体增殖物激活受体(PPARs)在调节细胞分化、增殖和胱天蛋白酶介导的细胞死亡途径中发挥着至关重要的作用。它们被认为是抗肿瘤药物开发的有前景的靶点,特别是针对多发性骨髓瘤(MM)和不同的血液系统恶性肿瘤。进行了几项早期临床试验,以衡量PPAR激动剂,特别是PPARα和PPARγ激动剂对各种癌症的临床实用性。广泛的研究已经调查了PPARs在代谢调节中的表达。此外,有人认为,仔细设计PPARs的部分激动剂可能会显示出副作用的改善,并增加治疗价值。本文综述了PPARs的有机化学和代谢作用,以及其激动剂在临床开发中的治疗潜力。研究血液系统恶性肿瘤的治疗剂。
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Role of PPAR Receptor and Ligands in the Pathogenesis and Therapy of Hematologic Malignancies
The Peroxisome proliferator-activated receptors (PPARs) play vital roles in regulating cellular differentiation, proliferation, and caspase-mediated cell death pathways. They are regarded as promising targets for anti-tumor drug development, particularly for multiple myeloma (MM) and different hematological malignancies. Several early section clinical trials are conducted to measure the clinical practicableness of PPAR agonists, notably PPARα and PPARγ agonists, against various cancers. A spread of studies has investigated PPARs expression in metabolic regulation. Furthermore, it has been suggested that careful designing of partial agonists for PPARs may show improvement with side effects and increase the therapeutic value. This review summarizes the organic chemistry and metabolic actions of PPARs, and the therapeutic potential of their agonists underneath clinical development. It investigates therapeutic agents for hematologic malignancies.
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CiteScore
1.30
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0.00%
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审稿时长
11 weeks
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