Lytix Biopharma AS , Sykehusveien 21, NO-9294 Tromsø, Norway.
Department of Chemistry and Centre for Pharmacy, University of Bergen , Allégaten 41, NO-5007 Bergen, Norway.
J Med Chem. 2016 Apr 14;59(7):2918-27. doi: 10.1021/acs.jmedchem.5b02025. Epub 2016 Mar 29.
Oncolytic immunotherapies represent a new promising strategy in the treatment of cancer. In our efforts to develop oncolytic peptides, we identified a series of chemically modified 9-mer cationic peptides that were highly effective against both drug-resistant and drug-sensitive cancer cells and with lower toxicity toward normal cells. Among these peptides, LTX-315 displayed superior anticancer activity and was selected as a lead candidate. This peptide showed relative high plasma protein binding abilities and a human plasma half-life of 160 min, resulting in formation of nontoxic metabolites. In addition, the lead candidate demonstrated relatively low ability to inhibit CYP450 enzymes. Collectively these data indicated that this peptide has potential to be developed as a new anticancer agent for intratumoral administration and is currently being evaluated in a phase I/IIa study.
溶瘤免疫疗法是癌症治疗的一种新的有前途的策略。在我们开发溶瘤肽的努力中,我们鉴定了一系列化学修饰的 9 肽阳离子肽,它们对耐药性和敏感性癌细胞均具有高度有效性,且对正常细胞的毒性较低。在这些肽中,LTX-315 表现出优越的抗癌活性,被选为先导候选物。该肽显示出相对较高的血浆蛋白结合能力和 160 分钟的人血浆半衰期,导致形成无毒的代谢物。此外,该候选药物对 CYP450 酶的抑制能力相对较低。这些数据表明,该肽具有作为一种新型抗肿瘤剂用于瘤内给药的潜力,目前正在一项 I/IIa 期研究中进行评估。