靶向MDM2-p53蛋白相互作用的新型戊烯基查尔酮:合成及抗肿瘤活性评价

Pedro Brandão, J. A. Loureiro, S. G. M. Carvalho, Meriem Hadjer Hamadou, S. Cravo, J. Moreira, D. Pereira, M. Pinto, H. Cidade
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引用次数: 0

摘要

在黄酮类化合物的化学领域中,烯丙基化衍生物因其具有多种生物活性而备受关注,其中查尔酮因其对多种肿瘤细胞系具有抗肿瘤活性而被广泛报道。事实上,已经证明,类黄酮的异戊二烯化显著增加了其对人类肿瘤细胞系[2]的生长抑制作用。我们合成了一系列戊烯基查尔酮,并利用酵母实验[3]评估了它们抑制MDM2-p53相互作用的能力。我们对所有合成的烯丙基查尔酮及其非烯丙基前体抑制人结肠癌HCT116细胞生长的能力进行了评价和比较。总体结果导致鉴定出一种hit化合物,该化合物在酵母中表现为MDM2-p53相互作用的潜在抑制剂,并且对表达野生型p53的人类肿瘤细胞表现出改善的细胞毒性。在HCT116癌细胞中,也发现这种烯丙基查尔酮的生长抑制作用与诱导细胞周期阻滞和凋亡有关。S. Venturelli等。营养学报,2016,32(11-12),1171-1178。M.P. Neves等。化学。Biodivers。中文信息学报,2012,9,1133-1143。P. Brandao等。中华医学杂志,2018,26(5):711-721。本研究部分由战略基金UID/Multi/04423/2013和UID/Multi/ 04378/2013通过FCT和ERDF提供的国家基金支持,在PT2020计划框架内,项目poci -01-0145-联邦-028736,PTDC/MAR-BIO/4694/2014(参考文献poci -01-0145-联邦-016790;项目3599-PPCDT), PTDC/AAGTEC/0739/2014(参考文献poci -01-0145- federal -016793;项目9471-PPCDT), PTDC/DTPFTO/1981/2014(参考文献pocl -01-0145-联邦-016581),以及INNOVMAR -海洋资源管理和开发中的创新和可持续性项目(参考文献NORTE-01-0145-联邦-000035,研究线NOVELMAR),由北葡萄牙区域业务计划(NORTE 2020)根据葡萄牙2020伙伴关系协议通过欧洲区域发展基金(ERDF)提供支持。
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New prenylchalcones targeting the MDM2-p53 protein-protein interaction: synthesis and evaluation of antitumor activity
Among the chemical world of flavonoids, prenylated derivatives have been attracting the attention because of the myriad of their biological activities, with chalcones being widely reported for their antitumor activity against a variety of tumor cell lines [1]. In fact, it has been demonstrated that isoprenylation of flavonoids significantly increased their growth inhibitory effect on human tumor cell lines [2]. A series of prenylchalcones was synthesized and evaluated for the ability to inhibit the MDM2-p53 interaction using a yeast-based assay [3]. The capacity of all synthesized prenylchalcones and their non-prenylated precursors to inhibit the growth of human colon tumor HCT116 cells was evaluated and compared [3]. The overall results led to the identification of a hit compound, which behaved as potential inhibitor of the MDM2-p53 interaction in yeast, and showed improved cytotoxicity against human tumor cells expressing wild-type p53. In HCT116 cancer cells, it was also shown that the growth inhibitory effect of this prenylchalcone was associated with the induction of cell cycle arrest, and apoptosis. S. Venturelli et al. Nutrition, 2016, 32(11-12), 1171-1178. M.P. Neves et al. Chem. Biodivers., 2012, 9, 1133-1143. P. Brandao et al. Eur J Med Chem, 2018, 156, 711-721. This research was partially supported by the Strategic Funding UID/Multi/04423/2013 and UID/MULTI/04378/2013 through national funds provided by FCT and ERDF, in the framework of the programme PT2020, the projects POCI-01-0145-FEDER-028736, PTDC/MAR-BIO/4694/2014 (reference POCI-01-0145-FEDER-016790; Project 3599–PPCDT), PTDC/AAGTEC/0739/2014 (reference POCI-01-0145-FEDER-016793; Project 9471–PPCDT), and PTDC/DTPFTO/1981/2014 (reference POCl-01-0145-FEDER-016581), as well as by the project INNOVMAR - Innovation and Sustainability in the Management and Exploitation of Marine Resources (reference NORTE-01-0145-FEDER-000035, within Research Line NOVELMAR), supported by North Portugal Regional Operational Programme (NORTE 2020), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (ERDF).
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