{"title":"肿瘤微环境响应纳米簇的时间分辨腹腔热化疗/热治疗对结直肠癌腹膜转移的影响。","authors":"Qiping Wu, Nanzhou Wang, Shiwen Wang, Zichao Wang, Yujie Li*, Yuanhong Xu* and Ying Shen*, ","doi":"10.1021/acsabm.5c00882","DOIUrl":null,"url":null,"abstract":"<p >Peritoneal metastasis (PM) originating from gastrointestinal cancer was considered a terminal disease until recently. It poses significant therapeutic challenges due to its diffuse nature and barriers to effective drug delivery. While locoregional approaches such as hyperthermic intraperitoneal chemotherapy (HIPEC) extend survival, their efficacy is constrained by systemic toxicity and tumor thermoresistance. To address these issues, we developed a tumor microenvironment-responsive nanocluster system (MoNs@MyC) for augmented HIPEC treatment. Comprising ultrasmall monodispersed-nanoclusters (MoNs) and clinically used HIPEC drug mitomycin C (MyC), MoNs@MyC self-assembles into microsize particles in acidic PM tumor environments, significantly enhancing localized drug retention during HIPEC. Its photothermal conversion ability enables noninvasive, time-resolved secondary hyperthermia therapy to synergize with chemotherapy and circumvent the thermoresistance of cancer cells. Furthermore, MoNs@MyC selectively mitigates the MyC-induced oxidative damage in healthy tissues. In PM mouse models, MoNs@MyC outperformed conventional MyC-based HIPEC, achieving superior tumor control and stimulating antitumor immunity via T-cell infiltration and pro-inflammatory cytokine upregulation. With scalable synthesis and cost-effective design, this dual-responsive system represents a transformative strategy for precision PM therapy, bridging the gap between localized treatment efficacy and systemic safety.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":"8 8","pages":"7113–7125"},"PeriodicalIF":4.7000,"publicationDate":"2025-08-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Tumor Microenvironment-Responsive Nanocluster for Time-Resolved Hyperthermic Intraperitoneal Chemo/Thermal-Therapy against Colorectal Peritoneal Metastasis\",\"authors\":\"Qiping Wu, Nanzhou Wang, Shiwen Wang, Zichao Wang, Yujie Li*, Yuanhong Xu* and Ying Shen*, \",\"doi\":\"10.1021/acsabm.5c00882\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Peritoneal metastasis (PM) originating from gastrointestinal cancer was considered a terminal disease until recently. It poses significant therapeutic challenges due to its diffuse nature and barriers to effective drug delivery. While locoregional approaches such as hyperthermic intraperitoneal chemotherapy (HIPEC) extend survival, their efficacy is constrained by systemic toxicity and tumor thermoresistance. To address these issues, we developed a tumor microenvironment-responsive nanocluster system (MoNs@MyC) for augmented HIPEC treatment. Comprising ultrasmall monodispersed-nanoclusters (MoNs) and clinically used HIPEC drug mitomycin C (MyC), MoNs@MyC self-assembles into microsize particles in acidic PM tumor environments, significantly enhancing localized drug retention during HIPEC. Its photothermal conversion ability enables noninvasive, time-resolved secondary hyperthermia therapy to synergize with chemotherapy and circumvent the thermoresistance of cancer cells. Furthermore, MoNs@MyC selectively mitigates the MyC-induced oxidative damage in healthy tissues. In PM mouse models, MoNs@MyC outperformed conventional MyC-based HIPEC, achieving superior tumor control and stimulating antitumor immunity via T-cell infiltration and pro-inflammatory cytokine upregulation. With scalable synthesis and cost-effective design, this dual-responsive system represents a transformative strategy for precision PM therapy, bridging the gap between localized treatment efficacy and systemic safety.</p>\",\"PeriodicalId\":2,\"journal\":{\"name\":\"ACS Applied Bio Materials\",\"volume\":\"8 8\",\"pages\":\"7113–7125\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2025-08-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Bio Materials\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acsabm.5c00882\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsabm.5c00882","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
Tumor Microenvironment-Responsive Nanocluster for Time-Resolved Hyperthermic Intraperitoneal Chemo/Thermal-Therapy against Colorectal Peritoneal Metastasis
Peritoneal metastasis (PM) originating from gastrointestinal cancer was considered a terminal disease until recently. It poses significant therapeutic challenges due to its diffuse nature and barriers to effective drug delivery. While locoregional approaches such as hyperthermic intraperitoneal chemotherapy (HIPEC) extend survival, their efficacy is constrained by systemic toxicity and tumor thermoresistance. To address these issues, we developed a tumor microenvironment-responsive nanocluster system (MoNs@MyC) for augmented HIPEC treatment. Comprising ultrasmall monodispersed-nanoclusters (MoNs) and clinically used HIPEC drug mitomycin C (MyC), MoNs@MyC self-assembles into microsize particles in acidic PM tumor environments, significantly enhancing localized drug retention during HIPEC. Its photothermal conversion ability enables noninvasive, time-resolved secondary hyperthermia therapy to synergize with chemotherapy and circumvent the thermoresistance of cancer cells. Furthermore, MoNs@MyC selectively mitigates the MyC-induced oxidative damage in healthy tissues. In PM mouse models, MoNs@MyC outperformed conventional MyC-based HIPEC, achieving superior tumor control and stimulating antitumor immunity via T-cell infiltration and pro-inflammatory cytokine upregulation. With scalable synthesis and cost-effective design, this dual-responsive system represents a transformative strategy for precision PM therapy, bridging the gap between localized treatment efficacy and systemic safety.
期刊介绍:
ACS Applied Bio Materials is an interdisciplinary journal publishing original research covering all aspects of biomaterials and biointerfaces including and beyond the traditional biosensing, biomedical and therapeutic applications.
The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrates knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important bio applications. The journal is specifically interested in work that addresses the relationship between structure and function and assesses the stability and degradation of materials under relevant environmental and biological conditions.