{"title":"光疗纳米致敏剂解锁多命中策略抑制肝癌肿瘤干性和增强索拉非尼反应。","authors":"Tian Qin, , , Huaze Lu, , , Qin Wang, , , Ying Deng, , , Jingtong Zeng, , , Yuanyuan Chen*, , and , Xinhong Liao*, ","doi":"10.1021/acsami.5c13211","DOIUrl":null,"url":null,"abstract":"<p >Tumor stemness, possessing self-renewal capabilities and high tumor-initiating potential, is one of the determinants of resilience against sorafenib for hepatocellular carcinoma (HCC). In this regard, a facile construction of the multityrosine kinase inhibitor sorafenib conjugated with black phosphorus nanosheets was demonstrated (denoted as BPS), which integrated multiple and distinctive properties, including effective stemness inhibition, mitochondria metabolic disruption, ferroptosis amplification, sorafenib resistance reversal, and outstanding photothermal conversion efficiency. Both <i>in vitro</i> and <i>in vivo</i> analyses collectively demonstrated that the proposed nanoplatform exhibited remarkable potential for synergistic photodynamic–photothermal therapies. Besides, the BPS-mediated tumor-associated macrophage epigenetic repolarization was highly beneficial for relieving immunosuppression and overcoming sorafenib resistance. Such a comprehensive structure optimization strategy provides a cooperative tumor stemness suppression–sorafenib resistance disarming approach for the treatment of HCC.</p>","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":"17 39","pages":"54537–54552"},"PeriodicalIF":8.2000,"publicationDate":"2025-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Phototherapy Nanosensitizer-Unlocked Multihit Strategy to Inhibit Tumor Stemness and Potentiate Sorafenib Response in Hepatocellular Carcinoma\",\"authors\":\"Tian Qin, , , Huaze Lu, , , Qin Wang, , , Ying Deng, , , Jingtong Zeng, , , Yuanyuan Chen*, , and , Xinhong Liao*, \",\"doi\":\"10.1021/acsami.5c13211\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Tumor stemness, possessing self-renewal capabilities and high tumor-initiating potential, is one of the determinants of resilience against sorafenib for hepatocellular carcinoma (HCC). In this regard, a facile construction of the multityrosine kinase inhibitor sorafenib conjugated with black phosphorus nanosheets was demonstrated (denoted as BPS), which integrated multiple and distinctive properties, including effective stemness inhibition, mitochondria metabolic disruption, ferroptosis amplification, sorafenib resistance reversal, and outstanding photothermal conversion efficiency. Both <i>in vitro</i> and <i>in vivo</i> analyses collectively demonstrated that the proposed nanoplatform exhibited remarkable potential for synergistic photodynamic–photothermal therapies. Besides, the BPS-mediated tumor-associated macrophage epigenetic repolarization was highly beneficial for relieving immunosuppression and overcoming sorafenib resistance. Such a comprehensive structure optimization strategy provides a cooperative tumor stemness suppression–sorafenib resistance disarming approach for the treatment of HCC.</p>\",\"PeriodicalId\":5,\"journal\":{\"name\":\"ACS Applied Materials & Interfaces\",\"volume\":\"17 39\",\"pages\":\"54537–54552\"},\"PeriodicalIF\":8.2000,\"publicationDate\":\"2025-09-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Materials & Interfaces\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acsami.5c13211\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Materials & Interfaces","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsami.5c13211","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
A Phototherapy Nanosensitizer-Unlocked Multihit Strategy to Inhibit Tumor Stemness and Potentiate Sorafenib Response in Hepatocellular Carcinoma
Tumor stemness, possessing self-renewal capabilities and high tumor-initiating potential, is one of the determinants of resilience against sorafenib for hepatocellular carcinoma (HCC). In this regard, a facile construction of the multityrosine kinase inhibitor sorafenib conjugated with black phosphorus nanosheets was demonstrated (denoted as BPS), which integrated multiple and distinctive properties, including effective stemness inhibition, mitochondria metabolic disruption, ferroptosis amplification, sorafenib resistance reversal, and outstanding photothermal conversion efficiency. Both in vitro and in vivo analyses collectively demonstrated that the proposed nanoplatform exhibited remarkable potential for synergistic photodynamic–photothermal therapies. Besides, the BPS-mediated tumor-associated macrophage epigenetic repolarization was highly beneficial for relieving immunosuppression and overcoming sorafenib resistance. Such a comprehensive structure optimization strategy provides a cooperative tumor stemness suppression–sorafenib resistance disarming approach for the treatment of HCC.
期刊介绍:
ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.