中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
The design of small-molecule prodrugs and activatable phototherapeutics for cancer therapy

文献类型:期刊论文

作者Han, Hai-Hao1,2,3,5,9; Wang, Han-Min1,5; Jangili, Paramesh6; Li, Mingle6; Wu, Luling4; Zang, Yi5; Sedgwick, Adam C.7; Li, Jia1,5,9; He, Xiao-Peng2,3,10,11; James, Tony D.4,8
刊名CHEMICAL SOCIETY REVIEWS
出版日期2023-02-06
卷号52期号:3页码:879-920
ISSN号0306-0012
DOI10.1039/d2cs00673a
通讯作者Wu, Luling(wllcyl@126.com) ; Sedgwick, Adam C.(adam.sedgwick@chem.ox.ac.uk) ; Li, Jia(jli@simm.ac.cn) ; He, Xiao-Peng(xphe@ecust.edu.cn) ; James, Tony D.(t.d.james@bath.ac.uk) ; Kim, Jong Seung(jongskim@korea.ac.kr)
英文摘要Cancer remains as one of the most significant health problems, with approximately 19 million people diagnosed worldwide each year. Chemotherapy is a routinely used method to treat cancer patients. However, current treatment options lack the appropriate selectivity for cancer cells, are prone to resistance mechanisms, and are plagued with dose-limiting toxicities. As such, researchers have devoted their attention to developing prodrug-based strategies that have the potential to overcome these limitations. This tutorial review highlights recently developed prodrug strategies for cancer therapy. Prodrug examples that provide an integrated diagnostic (fluorescent, photoacoustic, and magnetic resonance imaging) response, which are referred to as theranostics, are also discussed. Owing to the non-invasive nature of light (and X-rays), we have discussed external excitation prodrug strategies as well as examples of activatable photosensitizers that enhance the precision of photodynamic therapy/photothermal therapy. Activatable photosensitizers/photothermal agents can be seen as analogous to prodrugs, with their phototherapeutic properties at a specific wavelength activated in the presence of disease-related biomarkers. We discuss each design strategy and illustrate the importance of targeting biomarkers specific to the tumour microenvironment and biomarkers that are known to be overexpressed within cancer cells. Moreover, we discuss the advantages of each approach and highlight their inherent limitations. We hope in doing so, the reader will appreciate the current challenges and available opportunities in the field and inspire subsequent generations to pursue this crucial area of cancer research.
WOS关键词GAMMA-GLUTAMYL-TRANSPEPTIDASE ; RESPONSIVE DRUG-DELIVERY ; HYDROGEN-PEROXIDE ; TUMOR MICROENVIRONMENT ; PHOTODYNAMIC THERAPY ; OXIDATIVE STRESS ; RATIONAL DESIGN ; NANOPARTICLES ; DOXORUBICIN ; SYSTEMS
资助项目National Natural Science Foundation of China[21788102] ; National Natural Science Foundation of China[91853201] ; National Natural Science Foundation of China[9185920077] ; National Natural Science Foundation of China[82130099] ; National Natural Science Foundation of China[82151219] ; National Natural Science Foundation of China[31871414] ; National Natural Science Foundation of China[81971265] ; Shanghai Municipal Science and Technology Major Project[2018SHZDZX03] ; Shanghai Municipal Science and Technology Major Project[22ZR1415200] ; National Science Foundation of Shanghai[21XD1404600] ; National Science Foundation of Shanghai[21JC1406600] ; National Science Foundation of Shanghai[22140901000] ; International Cooperation Program of Shanghai Science and Technology Committee[17520750100] ; Fundamental Research Funds for the Central Universities[222201717003] ; Programme of Introducing Talents of Discipline to Universities[B16017] ; China Postdoctoral Science Foundation[2020M681196] ; Royal Society ; Open Research Fund of the School of Chemistry and Chemical Engineering, Henan Normal University[2020ZD01] ; China Scholarship Council ; University of Bath ; National Research Foundation of Korea (CRI project)[2018R1A3B1052702] ; National Research Foundation of Korea (CRI project)[2019M3E5D1A01068998] ; Brain Pool Program through the National Research Foundation of Korea (NRF) - Ministry of Science and ICT[2020H1D3A1A02080172] ; Glasstone Research fellowship (University of Oxford) ; Jesus College, Oxford
WOS研究方向Chemistry
语种英语
出版者ROYAL SOC CHEMISTRY
WOS记录号WOS:000913076000001
源URL[http://119.78.100.183/handle/2S10ELR8/303528]  
专题新药研究国家重点实验室
通讯作者Wu, Luling; Sedgwick, Adam C.; Li, Jia; He, Xiao-Peng; James, Tony D.; Kim, Jong Seung
作者单位1.Univ Chinese Acad Sci, 19A Yuquan Rd, Beijing 100049, Peoples R China
2.East China Univ Sci & Technol, Sch Chem & Mol Engn, Key Lab Adv Mat, 130 Meilong Rd, Shanghai 200237, Peoples R China
3.East China Univ Sci & Technol, Sch Chem & Mol Engn, Feringa Nobel Prize Scientist Joint Res Ctr, Frontiers Ctr Materiobiol & Dynam Chem,Joint Int R, 130 Meilong Rd, Shanghai 200237, Peoples R China
4.Univ Bath, Dept Chem, Bath BA2 7AY, England
5.Chinese Acad Sci, Shanghai Inst Mat Med, Mol Imaging Ctr, State Key Lab Drug Res, Shanghai 201203, Peoples R China
6.Korea Univ, Dept Chem, Seoul 02841, South Korea
7.Univ Oxford, Chem Res Lab, Mansfield Rd, Oxford OX1 3TA, England
8.Henan Normal Univ, Sch Chem & Chem Engn, Xinxiang 453007, Peoples R China
9.Bohai Rim Adv Res Inst Drug Discovery, Shandong Lab Yantai Drug Discovery, Yantai 264117, Shandong, Peoples R China
10.Eastern Hepatobiliary Surg Hosp, Int Cooperat Lab Signal Transduct, Shanghai 200438, Peoples R China
推荐引用方式
GB/T 7714
Han, Hai-Hao,Wang, Han-Min,Jangili, Paramesh,et al. The design of small-molecule prodrugs and activatable phototherapeutics for cancer therapy[J]. CHEMICAL SOCIETY REVIEWS,2023,52(3):879-920.
APA Han, Hai-Hao.,Wang, Han-Min.,Jangili, Paramesh.,Li, Mingle.,Wu, Luling.,...&Kim, Jong Seung.(2023).The design of small-molecule prodrugs and activatable phototherapeutics for cancer therapy.CHEMICAL SOCIETY REVIEWS,52(3),879-920.
MLA Han, Hai-Hao,et al."The design of small-molecule prodrugs and activatable phototherapeutics for cancer therapy".CHEMICAL SOCIETY REVIEWS 52.3(2023):879-920.

入库方式: OAI收割

来源:上海药物研究所

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