酚肽作为抗氧化剂和抗增殖剂

Azucena Marset-Castro, Álvaro López-Gallardo, H. López-Muñoz, L. Sánchez-Sánchez, Inés Maya, Ó. López, J. Fernández-Bolaños
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引用次数: 3

摘要

我们报道了从3,4-二羟基苯乙酸(DOPAC)和l配置的氨基酸酯(甘氨酸、苯丙氨酸、缬氨酸、丝氨酸、色氨酸和胱氨酸)开始,使用不同的偶联剂高效合成酚肽。酚醛支架与氨基酸残基的结合可能会调节标题衍生物的生物利用度和治疗特性。此外,具有固有氧化还原活性的儿茶酚基团的掺入可以改变癌细胞的氧化还原状态,从而提供抗增殖特性。对三种人宫颈癌细胞系(HeLa、ViBo和CaSki)和正常淋巴细胞的抗氧化活性(即清除自由基和H2O2以及抑制脂质过氧化)和抗增殖活性进行了评价。所有化合物均表现出优异的抗氧化活性;值得注意的是,从l-胱氨酸中提取的肽具有最好的抗氧化活性,与天然的2-(3 ',4 ' -二羟基苯基)乙醇(hydroxytyrosol, HT)相比,其自由基清除活性提高了2.5倍。此外,该化合物对3种人类肿瘤细胞系的抗肿瘤活性最强(IC50值为108 ~ 122 μM),与天然DOPAC和HT相比,其活性提高了2 ~ 7倍。重要的是,这些酚类肽模拟物对正常人类淋巴细胞的细胞毒活性非常低,从而证实了它们对肿瘤细胞的选择性。此外,与正常淋巴细胞相比,含二硫肽也表现出可忽略不计的细胞坏死和对肿瘤细胞的高选择性。该衍生物包含两个具有氧化还原特性的片段,儿茶酚段和二硫连接体。因此,含二硫化物的酚类肽模拟物成为开发新型抗肿瘤药物家族的良好候选者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phenolic peptides as antioxidant and anti-proliferative agents
We report an efficient synthesis of phenolic peptides starting from 3,4-dihydroxyphenylacetic acid (DOPAC) and L-configured amino acid esters (glycine, phenylalanine, valine, serine, tryptophan, and cystine) using different coupling reagents. The combination of a phenolic scaffold with an amino acid residue might modulate the bioavailability and the therapeutic properties of title derivatives. Moreover, the incorporation of a catechol group, with inherent redox activity, can contribute to alter the redox status of the cancer cells, and therefore, provide anti-proliferative properties. Their activities as antioxidants (i.e. scavenging free radicals and H2O2 as well inhibition of lipid peroxidation) and as anti-proliferative agents against three human cervical carcinoma cell lines (HeLa, ViBo, and CaSki) and normal lymphocytes were evaluated. All compounds exhibited an excellent antioxidant activity; remarkably, the peptide derived from L-cystine exhibited the best antioxidant activity, displaying a 2.5-fold increase in radical-scavenging activity when compared with the natural 2-(3’,4’-dihydroxyphenyl)ethanol (hydroxytyrosol, HT). Moreover, this compound was also the most potent antitumor agent against the three human tumor cell lines (IC50 values 108-122 μM), with a 2-7-fold increase in activity when compared with natural DOPAC and HT, used as reference compounds. Importantly, the cytotoxic activity of these phenolic peptidomimetics against normal human lymphocytes was very low, hence confirming their selectivity towards tumor cells. Moreover, a disulfide-containing peptide also exhibited negligible cell necrosis and a high selectivity against tumor cells when compared to normal lymphocytes. Such derivative incorporates two fragments characterized with redox properties, the catechol moiety, and the disulfide linker. Thus, disulfide-containing phenolic peptidomimetics emerge as good lead candidates for the development of a novel family of anti-tumor agents.
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