Kuttikrishnan Shilpa, Prabhu Kirti S, Al Sharie Ahmed H, Al Zu'bi Yazan O, Alali Feras Q, Oberlies Nicholas H, Ahmad Aamir, El-Elimat Tamam, Uddin Shahab
Translational Research Institute, Academic Health System, Hamad Medical Corporation, Doha, Qatar; Biomedical and Pharmaceutical Research Unit, QU Health, Qatar University, Doha, Qatar.
Translational Research Institute, Academic Health System, Hamad Medical Corporation, Doha, Qatar.
Drug Discov Today. 2022 Feb;27(2):547-557. doi: 10.1016/j.drudis.2021.10.001. Epub 2021 Oct 13.
Resorcylic acid lactones (RALs) are fungal polyketides that consist of a β-resorcylic acid residue (2,4-dihydroxybenzoic acid) embedded in a macrolactone ring. RALs exhibit a broad range of biological activities, including anticancer activities. Following discovery of the selective Hsp90 inhibition activity of radicicol, the kinase inhibition activity of hypothemycin, monocillin II, 5Z-7-oxo-zeaenol, and L-783,277 RALs, and the nuclear factor kappa B (NF-κB) inhibition activity of the RAL zearalenone, have attracted great attention as potential therapeutics for cancer treatment. In this minireview, we focus on natural RALs that possess cytotoxic activities [IC values < 10 μM (or 4-5 μg/ml)], discussing their structures, isolation, occurrence, biological activities, and anticancer molecular mechanisms.
间苯二酚内酯(RALs)是一类真菌聚酮化合物,由嵌入大环内酯环中的β-间苯二酚残基(2,4-二羟基苯甲酸)组成。RALs具有广泛的生物活性,包括抗癌活性。继发现萝卜灵具有选择性热休克蛋白90(Hsp90)抑制活性、腐草霉素、单青霉素II、5Z-7-氧代-玉米烯醇和L-783,277 RALs具有激酶抑制活性,以及RAL玉米赤霉烯酮具有核因子κB(NF-κB)抑制活性之后,它们作为癌症治疗的潜在疗法引起了极大关注。在本综述中,我们聚焦于具有细胞毒性活性[半数抑制浓度(IC)值<10μM(或4-5μg/ml)]的天然RALs,讨论它们的结构、分离、来源、生物活性和抗癌分子机制。