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Caerin 1.1和1.9肽可诱导上皮癌细胞发生急性半胱天冬酶3/ Gasdermin E介导的细胞焦亡。

Caerin 1.1 and 1.9 peptides induce acute caspase 3/GSDME-mediated pyroptosis in epithelial cancer cells.

作者信息

Luo Yuandong, Li Junjie, Fu Quanlan, Zhang Pingping, Song Xinyi, Liu Mengqi, Mo Rongmi, Fu Jiawei, Tang Shuxian, Wu Jialing, Yang Xiaodan, Liu Xiaosong, Wang Tianfang, Ni Guoying

机构信息

Medical College of Guizhou University, Guiyang, 550025, Guizhou, China.

Zhongao Biomedical Technology (Guangdong) Co. Ltd, Zhongshan, 528400, Guangdong, China.

出版信息

Sci Rep. 2025 Apr 18;15(1):13377. doi: 10.1038/s41598-025-96438-0.

Abstract

Caerin peptides exhibit a dual role in cancer treatment by directly killing cancer cells and modulating the tumour microenvironment to enhance anti-tumour immunity. This study investigates the mechanisms underlying caerin 1.1/1.9-induced acute cell death in epithelial cancer cells and explores their therapeutic potential. HeLa, A549, and Huh-7 cancer cell lines were treated with caerin 1.1/1.9 peptides. Morphological observations, flow cytometry, lactate dehydrogenase (LDH) release, and IL-18 secretion assays revealed the occurrence of pyroptosis following treatment. Specifically, a 1-h treatment with caerin 1.1/1.9 induced pyroptosis in HeLa, A549, and Huh-7 cells, characterised by cell swelling, membrane bubbling, and the release of IL-18 and LDH. Western blotting confirmed the upregulation of pyroptosis markers, including caspase-3, cleaved caspase-3, and GSDME-N fragments. These findings highlight the significant role of caerin peptides in inducing acute pyroptosis, a form of programmed cell death that enhances the immunogenicity of dying cancer cells, thus potentially improving the effectiveness of immunotherapies. This research underscores the therapeutic potential of caerin 1.1/1.9 peptides in cancer treatment, providing a foundation for developing new anti-cancer strategies that leverage both direct cytotoxic effects and immune modulation to achieve more effective and sustained anti-tumour responses.

摘要

凯林肽在癌症治疗中发挥着双重作用,既能直接杀死癌细胞,又能调节肿瘤微环境以增强抗肿瘤免疫力。本研究调查了凯林1.1/1.9诱导上皮癌细胞急性细胞死亡的潜在机制,并探索了它们的治疗潜力。用凯林1.1/1.9肽处理HeLa、A549和Huh-7癌细胞系。形态学观察、流式细胞术、乳酸脱氢酶(LDH)释放和IL-18分泌测定显示处理后发生了细胞焦亡。具体而言,用凯林1.1/1.9处理1小时可诱导HeLa、A549和Huh-7细胞发生细胞焦亡,其特征为细胞肿胀、膜起泡以及IL-18和LDH的释放。蛋白质免疫印迹法证实了细胞焦亡标志物的上调,包括半胱天冬酶-3、裂解的半胱天冬酶-3和GSDME-N片段。这些发现突出了凯林肽在诱导急性细胞焦亡中的重要作用,细胞焦亡是一种程序性细胞死亡形式,可增强垂死癌细胞的免疫原性,从而有可能提高免疫疗法的有效性。本研究强调了凯林1.1/1.9肽在癌症治疗中的治疗潜力,为开发新的抗癌策略提供了基础,这些策略利用直接的细胞毒性作用和免疫调节来实现更有效和持续的抗肿瘤反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04c6/12008296/c330b67769de/41598_2025_96438_Fig1_HTML.jpg

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