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用于肺癌治疗的新型蛙皮衍生肽皮防御素-PP:评估及抗肿瘤机制研究

Novel Frog Skin-Derived Peptide Dermaseptin-PP for Lung Cancer Treatment: Evaluation and Anti-tumor Mechanisms Study.

作者信息

Dong Ziyi, Hu Haiyan, Yu Xianglong, Tan Li, Ma Chengbang, Xi Xinping, Li Lei, Wang Lei, Zhou Mei, Chen Tianbao, Du Shouying, Lu Yang

机构信息

Laboratory of Traditional Chinese Medicine, School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, China.

Livzon Pharmaceutical Group Inc., Zhuhai, China.

出版信息

Front Chem. 2020 Jun 5;8:476. doi: 10.3389/fchem.2020.00476. eCollection 2020.

Abstract

Lung cancer is the major cause of cancer deaths worldwide, and it has the highest incidence and mortality rate of any cancer among men and women in China. The first-line therapy for lung cancer treatment is platinum-based chemotherapy drugs such as cisplatin. However, the application of present chemotherapies is limited by severe side effects, which stimulates the discovery of new drugs with new anti-tumor mechanisms and fewer side effects. Beneficially, many antimicrobial peptides (AMPs) from frog skin have been reported to exhibit potent anti-cancer activities with low toxicity, high selectivity and a low propensity to induce resistance. In this study, we first reported an AMP named Dermaseptin-PP, from a rarely studied frog species, . Dermaseptin-PP exhibited selective cytotoxicity on H157, MCF-7, PC-3, and U251 MG cancer cells instead of normal HMEC-1 cells with low hemolytic effect. Furthermore, on subcutaneous H157 tumor model of nude mice, Dermaseptin-PP was found to display potent anti-tumor activity in a dose-related manner without obvious hepatopulmonary side effects. It is widely accepted that AMPs usually work through a membrane disruptive mode, and the confocal laser microscope observation confirmed that Dermaseptin-PP could destroy H157 cell membranes. Further investigation of mechanisms by flow cytometry assay and immunohistochemical analysis unraveled that Dermaseptin-PP also exerted its anti-tumor activity by inducing H157 cell apoptosis via both endogenous mitochondrial apoptosis pathway and exogenous death receptor apoptosis pathway. Herein, we emphasize that the membrane disrupting and the apoptosis activation effects of Dermaseptin-PP both depend on its concentration. Overall, a novel frog skin-derived AMP, named Dermaseptin-PP, was identified for the first time. It possesses strong antimicrobial activity and effective anti-tumor activity by distinct mechanisms. This study revealed the possibility of Dermaseptin-PP for lung cancer treatment and provided a new perspective for designing novel AMP-based anti-tumor candidates with low risk of cytotoxicity.

摘要

肺癌是全球癌症死亡的主要原因,在中国男性和女性中,肺癌的发病率和死亡率在所有癌症中位居首位。肺癌治疗的一线疗法是使用顺铂等铂类化疗药物。然而,目前化疗的应用受到严重副作用的限制,这促使人们去发现具有新抗肿瘤机制且副作用较少的新药。幸运的是,许多来自蛙皮的抗菌肽(AMPs)已被报道具有强大的抗癌活性,毒性低、选择性高且诱导耐药的倾向低。在本研究中,我们首次报道了一种来自一种鲜为人研究的蛙类的抗菌肽,名为Dermaseptin-PP。Dermaseptin-PP对H157、MCF-7、PC-3和U251 MG癌细胞表现出选择性细胞毒性,而对正常的HMEC-1细胞无此作用,且溶血作用低。此外,在裸鼠皮下H157肿瘤模型中,发现Dermaseptin-PP以剂量相关的方式显示出强大的抗肿瘤活性,且无明显的肝肺副作用。人们普遍认为抗菌肽通常通过膜破坏模式发挥作用,共聚焦激光显微镜观察证实Dermaseptin-PP可破坏H157细胞膜。通过流式细胞术分析和免疫组织化学分析对机制进行的进一步研究表明,Dermaseptin-PP还通过内源性线粒体凋亡途径和外源性死亡受体凋亡途径诱导H157细胞凋亡,从而发挥其抗肿瘤活性。在此,我们强调Dermaseptin-PP的膜破坏和凋亡激活作用均取决于其浓度。总体而言,首次鉴定出一种新型的源自蛙皮的抗菌肽,名为Dermaseptin-PP。它具有强大的抗菌活性和通过不同机制发挥的有效抗肿瘤活性。本研究揭示了Dermaseptin-PP用于肺癌治疗的可能性,并为设计具有低细胞毒性风险的新型基于抗菌肽的抗肿瘤候选药物提供了新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37fc/7291860/0e2fb471eedc/fchem-08-00476-g0001.jpg

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