Department of Bioengineering, Zunyi Medical University Zhuhai Campus, Zhuhai, Guangdong 519040, People's Republic of China.
Zhuhai Key Laboratory of Fundamental and Applied Research in Traditional Chinese Medicine, Zunyi Medical University Zhuhai Campus, Zhuhai, Guangdong 519040, People's Republic of China.
Open Biol. 2020 Jul;10(7):200004. doi: 10.1098/rsob.200004. Epub 2020 Jul 22.
Anti-cancer peptides (ACPs) are a series of short peptides composed of 10-60 amino acids that can inhibit tumour cell proliferation or migration, or suppress the formation of tumour blood vessels, and are less likely to cause drug resistance. The aforementioned merits make ACPs the most promising anti-cancer candidate. However, ACPs may be degraded by proteases, or result in cytotoxicity in many cases. To overcome these drawbacks, a plethora of research has focused on reconstruction or modification of ACPs to improve their anti-cancer activity, while reducing their cytotoxicity. The modification of ACPs mainly includes main chain reconstruction and side chain modification. After summarizing the classification and mechanism of action of ACPs, this paper focuses on recent development and progress about their reconstruction and modification. The information collected here may provide some ideas for further research on ACPs, in particular their modification.
抗癌肽(ACPs)是一组由 10-60 个氨基酸组成的短肽,能够抑制肿瘤细胞增殖或迁移,或抑制肿瘤血管形成,且不太可能产生耐药性。上述优点使得 ACPs 成为最有前途的抗癌候选药物。然而,在许多情况下,ACPs 可能会被蛋白酶降解,或者导致细胞毒性。为了克服这些缺点,大量的研究集中在 ACPs 的重建或修饰上,以提高其抗癌活性,同时降低其细胞毒性。ACPs 的修饰主要包括主链重建和侧链修饰。在总结 ACPs 的分类和作用机制后,本文重点介绍了其重建和修饰的最新进展。这里收集的信息可能为进一步研究 ACPs,特别是其修饰提供一些思路。