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。

IF 4.7 Q2 MATERIALS SCIENCE, BIOMATERIALS
Qiping Wu, Nanzhou Wang, Shiwen Wang, Zichao Wang, Yujie Li*, Yuanhong Xu* and Ying Shen*, 
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引用次数: 0

摘要

直到最近,起源于胃肠道肿瘤的腹膜转移被认为是一种绝症。由于其弥漫性和有效给药的障碍,它给治疗带来了重大挑战。虽然局部方法如高温腹腔化疗(HIPEC)延长了生存期,但其疗效受到全身毒性和肿瘤耐热性的限制。为了解决这些问题,我们开发了一种肿瘤微环境响应纳米簇系统(MoNs@MyC),用于增强HIPEC治疗。MoNs@MyC由超小单分散纳米团簇(MoNs)和临床使用的HIPEC药物丝裂霉素C (MyC)组成,在酸性PM肿瘤环境中自组装成微颗粒,显著增强HIPEC过程中的局部药物保留。其光热转换能力使无创、时间解决的二次热疗与化疗协同作用,绕过癌细胞的热阻。此外,MoNs@MyC选择性地减轻了健康组织中myc诱导的氧化损伤。在PM小鼠模型中,MoNs@MyC优于传统的基于myc的HIPEC,通过t细胞浸润和促炎细胞因子上调实现卓越的肿瘤控制和刺激抗肿瘤免疫。凭借可扩展的合成和经济高效的设计,这种双反应系统代表了精确PM治疗的变革战略,弥合了局部治疗疗效和全身安全性之间的差距。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Tumor Microenvironment-Responsive Nanocluster for Time-Resolved Hyperthermic Intraperitoneal Chemo/Thermal-Therapy against Colorectal Peritoneal Metastasis

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.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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.
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