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Site-specific nanomodulator capable of modulation apoptosis for enhanced colorectal cancer chemo-photothermal therapy

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机构: [1]Institute for Cancer Medicine, School of Basic Medical Sciences,Southwest Medical University, Luzhou 646000, Sichuan, China [2]State Key Laboratory of Biotherapy and Cancer Center, West ChinaHospital, and West China, School of Basic Medical Sciences and ForensicMedicine, Collaborative Innovation Center for Biotherapy, SichuanUniversity, Chengdu 610041, China [3]Department of Biochemistry and Molecular Biology, Monash University,Clayton, VIC 3800, Australia [4]The Second Affiliated Hospital of Chengdu Medical College, ChinaNational Nuclear Corporation 416 Hospital, Chengdu 610051, Sichuan,China [5]Key Laboratory of Molecular Biology for Infectious Diseases (Ministryof Education), Institute for Viral Hepatitis, Department of InfectiousDiseases, the Second Affiliated Hospital, Chongqing Medical University,Chongqing 400016, China
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关键词: Colorectal cancer Celastrol IR820 Chemotherapy Photothermal therapy

摘要:
Colorectal cancer (CRC) is a common malignancy with the second highest mortality and the third highest morbidity worldwide. However, the overall survival of patients is unsatisfactory, thus requiring more effective clinical strategies. Celastrol (CLT), a natural bioactive compound, has been reported to induce reactive oxygen species (ROS)-mediated apoptosis to exhibit significant antitumor effects against CRC. However, the poor water solubility, low targeting ability, and bioavailability of CLT have limited its application, and CLT-induced protective autophagy weakens its therapeutic efficiency.We designed a targeted chemo-phototherapy nanoplatform (HCR NPs) to improve the application of CLT. The codelivery of IR820 and CLT in HCR NPs solved the water-soluble problem of CLT and enhanced apoptosis via IR820-mediated hyperthermia. In addition, hydroxychloroquine (HCQ) conjugated to hyaluronic acid (HA) not only increased the active targeting of HCR NPs but also inhibited CLT-induced protective autophagy to exacerbate apoptosis, thus achieving an amplified antitumor effect. Importantly, the HCR NPs exhibited an excellent therapeutic effect on CRC both in vitro and in vivo.The HCR NPs presented in this study may not merely provide a new reference for the clinical application of CLT but also result in an attractive strategy for CRC treatment.© 2023. The Author(s).

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出版当年[2023]版:
大类 | 1 区 生物学
小类 | 1 区 生物工程与应用微生物 2 区 纳米科技
最新[2023]版:
大类 | 1 区 生物学
小类 | 1 区 生物工程与应用微生物 2 区 纳米科技
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第一作者机构: [1]Institute for Cancer Medicine, School of Basic Medical Sciences,Southwest Medical University, Luzhou 646000, Sichuan, China
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