免疫系统
癌症研究
结直肠癌
医学
体内
癌症
姜黄素
免疫原性细胞死亡
益生菌
遗传增强
免疫疗法
基因工程
自杀基因
体外
转基因生物
免疫学
癌细胞
程序性细胞死亡
树突状细胞
抗原
生物
基因
作者
Jie Long,Tongrui Shang,Xuezhong Mo,Yunfang Yu,Lin Feng,Z Y Liang,Olivia Monteiro,Daniel Tomas Baptista‐Hon,Dominic Chi-chung Foo,Lui Ng,Renchuan Liang,Man Tong,Weizhong Tang,K C Zhang,Y Huang
出处
期刊:MedComm
[Wiley]
日期:2026-07-16
卷期号:7 (8): e70871-e70871
摘要
ABSTRACT Colorectal cancer (CRC) remains a leading cause of cancer‐related mortality worldwide, largely due to limitations in early diagnosis and effective treatment. To address these challenges, we developed a multifunctional probiotic nanoplatform, EcNA@Cur‐Lip‐FA, that integrates real‐time diagnosis, targeted therapy, and immune modulation for enhanced CRC treatment. Specifically, this system leverages genetically engineered Escherichia coli Nissle 1917 (EcN) encoding acoustic reporter genes (ARGs) to produce ultrasound (US)‐responsive gas vesicles (GVs), enabling real‐time, noninvasive tumor imaging. Simultaneously, folic acid (FA)‐modified curcumin‐loaded liposomes (Cur‐Lip‐FA) are co‐delivered with EcN, enhancing tumor‐specific accumulation and therapeutic precision. After being taken up by tumor cells, curcumin is released locally upon exposure to US irradiation, generating reactive oxygen species (ROS), inducing immunogenic cell death (ICD), and activating the cGAS‐STING pathway to promote dendritic cells (DCs) maturation and robust CD4 + /CD8 + T‐cell responses. Additionally, EcNA@Cur‐Lip‐FA downregulates angiogenesis‐related factors (VEGF, VEGFR1, and ANGPT1), thereby inhibiting tumor neovascularization. In vitro and in vivo studies demonstrated that EcNA@Cur‐Lip‐FA enables precise tumor localization, dynamic imaging, and effective suppression of both primary CRC and metastatic liver lesions with favorable biocompatibility. This multifunctional platform offers a promising strategy for integrating diagnosis and treatment, paving the way for next‐generation CRC theranostics.
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