Huizhen Li , Guixuan Fang , Wen Tian , Yinglin Liao , Jing Xiang , Yingying Hu , Lianxiang Luo
{"title":"积雪草酸通过诱导 SRC 介导的铁变态反应诱导肺癌毒性","authors":"Huizhen Li , Guixuan Fang , Wen Tian , Yinglin Liao , Jing Xiang , Yingying Hu , Lianxiang Luo","doi":"10.1016/j.taap.2024.117097","DOIUrl":null,"url":null,"abstract":"<div><p>Ferroptosis is a recently discovered form of regulated cell death that shows promise as a novel approach for inducing tumor cell death in cancer treatment, with significant research potential. Asiatic acid (AA), a key component of the traditional Chinese medicine <em>Centella asiatica</em>, has been identified as having potential therapeutic benefits for various diseases, particularly cancer. Non-small cell lung cancer (NSCLC) is a challenging and prevalent form of cancer to treat. In our study, we utilized network pharmacology, molecular docking, and experimental methods to investigate the potential of AA in treating NSCLC and to elucidate its role in inhibiting cancer through the ferroptosis pathway. Through network pharmacology analysis, we identified that AA targets the core NSCLC protein SRC through the ferroptosis pathway. Our experiments demonstrated that treatment with AA led to increased iron accumulation, mitochondrial membrane potential, and expression of ferroptosis markers glutathione peroxidase 4 (GPX4), ferritin heavy chain 1 (FTH1), and acyl-CoA synthetase long chain family member 4 (ACSL4) in NSCLC cells, confirming the induction of ferroptosis. In conclusion, AA has the potential to target SRC and induce NSCLC cell death through the ferroptosis pathway, offering a promising approach for cancer treatment.</p></div>","PeriodicalId":3,"journal":{"name":"ACS Applied Electronic Materials","volume":null,"pages":null},"PeriodicalIF":4.3000,"publicationDate":"2024-09-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0041008X24002953/pdfft?md5=9f07fe8f5848ba70843421f46d6ec8e7&pid=1-s2.0-S0041008X24002953-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Asiatic acid induces lung cancer toxicity by triggering SRC-mediated ferroptosis\",\"authors\":\"Huizhen Li , Guixuan Fang , Wen Tian , Yinglin Liao , Jing Xiang , Yingying Hu , Lianxiang Luo\",\"doi\":\"10.1016/j.taap.2024.117097\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Ferroptosis is a recently discovered form of regulated cell death that shows promise as a novel approach for inducing tumor cell death in cancer treatment, with significant research potential. Asiatic acid (AA), a key component of the traditional Chinese medicine <em>Centella asiatica</em>, has been identified as having potential therapeutic benefits for various diseases, particularly cancer. Non-small cell lung cancer (NSCLC) is a challenging and prevalent form of cancer to treat. In our study, we utilized network pharmacology, molecular docking, and experimental methods to investigate the potential of AA in treating NSCLC and to elucidate its role in inhibiting cancer through the ferroptosis pathway. Through network pharmacology analysis, we identified that AA targets the core NSCLC protein SRC through the ferroptosis pathway. Our experiments demonstrated that treatment with AA led to increased iron accumulation, mitochondrial membrane potential, and expression of ferroptosis markers glutathione peroxidase 4 (GPX4), ferritin heavy chain 1 (FTH1), and acyl-CoA synthetase long chain family member 4 (ACSL4) in NSCLC cells, confirming the induction of ferroptosis. In conclusion, AA has the potential to target SRC and induce NSCLC cell death through the ferroptosis pathway, offering a promising approach for cancer treatment.</p></div>\",\"PeriodicalId\":3,\"journal\":{\"name\":\"ACS Applied Electronic Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2024-09-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S0041008X24002953/pdfft?md5=9f07fe8f5848ba70843421f46d6ec8e7&pid=1-s2.0-S0041008X24002953-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Electronic Materials\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0041008X24002953\",\"RegionNum\":3,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENGINEERING, ELECTRICAL & ELECTRONIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Electronic Materials","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0041008X24002953","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, ELECTRICAL & ELECTRONIC","Score":null,"Total":0}
引用次数: 0
摘要
铁凋亡是最近发现的一种调节性细胞死亡形式,有望成为一种在癌症治疗中诱导肿瘤细胞死亡的新方法,具有巨大的研究潜力。积雪草酸(AA)是传统中药积雪草的一种主要成分,已被确认对多种疾病,尤其是癌症具有潜在的治疗作用。非小细胞肺癌(NSCLC)是一种具有挑战性的常见癌症。在我们的研究中,我们利用网络药理学、分子对接和实验方法研究了 AA 治疗 NSCLC 的潜力,并阐明了 AA 通过铁蛋白沉积途径抑制癌症的作用。通过网络药理学分析,我们发现 AA 可通过铁突变通路靶向 NSCLC 核心蛋白 SRC。我们的实验证明,用 AA 处理后,NSCLC 细胞中的铁积累、线粒体膜电位以及铁氧化标志物谷胱甘肽过氧化物酶 4 (GPX4)、铁蛋白重链 1 (FTH1) 和酰基-CoA 合成酶长链家族成员 4 (ACSL4) 的表达均增加,证实了铁氧化的诱导作用。总之,AA 有可能靶向 SRC 并通过铁蛋白沉积途径诱导 NSCLC 细胞死亡,为癌症治疗提供了一种前景广阔的方法。
Asiatic acid induces lung cancer toxicity by triggering SRC-mediated ferroptosis
Ferroptosis is a recently discovered form of regulated cell death that shows promise as a novel approach for inducing tumor cell death in cancer treatment, with significant research potential. Asiatic acid (AA), a key component of the traditional Chinese medicine Centella asiatica, has been identified as having potential therapeutic benefits for various diseases, particularly cancer. Non-small cell lung cancer (NSCLC) is a challenging and prevalent form of cancer to treat. In our study, we utilized network pharmacology, molecular docking, and experimental methods to investigate the potential of AA in treating NSCLC and to elucidate its role in inhibiting cancer through the ferroptosis pathway. Through network pharmacology analysis, we identified that AA targets the core NSCLC protein SRC through the ferroptosis pathway. Our experiments demonstrated that treatment with AA led to increased iron accumulation, mitochondrial membrane potential, and expression of ferroptosis markers glutathione peroxidase 4 (GPX4), ferritin heavy chain 1 (FTH1), and acyl-CoA synthetase long chain family member 4 (ACSL4) in NSCLC cells, confirming the induction of ferroptosis. In conclusion, AA has the potential to target SRC and induce NSCLC cell death through the ferroptosis pathway, offering a promising approach for cancer treatment.