Advancing Proteolysis Targeting Chimera (PROTAC) Nanotechnology in Protein Homeostasis Reprograming for Disease Treatment

被引:1
|
作者
Wu, Mengyao [1 ]
Zhao, Yilan [1 ]
Zhang, Chi [1 ]
Pu, Kanyi [2 ,3 ]
机构
[1] Huazhong Univ Sci & Technol, Hubei Engn Res Ctr Biomat & Med Protect Mat, Sch Chem & Chem Engn, Hubei Key Lab Bioinorgan Chem & Mat Med, Wuhan 430074, Peoples R China
[2] Nanyang Technol Univ, Sch Chem Chem Engn & Biotechnol, Singapore 637457, Singapore
[3] Nanyang Technol Univ, Lee Kong Chian Sch Med, Singapore 636921, Singapore
基金
中国国家自然科学基金; 新加坡国家研究基金会;
关键词
PROTAC; nanomedicine; cancer therapy; targeted protein degradation; protein homeostasis; disease treatment; nanoplatform; protein of interest; INDOLEAMINE 2,3-DIOXYGENASE EXPRESSION; TISSUE FERRITIN CONCENTRATION; TYROSINE PHOSPHATASE SHP-2; TGF-BETA; NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE; ANDROGEN RECEPTOR; THIOFLAVIN-T; IN-VIVO; GENOMIC ORGANIZATION; MOLECULAR-MECHANISM;
D O I
10.1021/acsnano.4c09800
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Proteolysis targeting chimeras (PROTACs) represent a transformative class of therapeutic agents that leverage the intrinsic protein degradation machinery to modulate the hemostasis of key disease-associated proteins selectively. Although several PROTACs have been approved for clinical application, suboptimal therapeutic efficacy and potential adverse side effects remain challenging. Benefiting from the enhanced targeted delivery, reduced systemic toxicity, and improved bioavailability, nanomedicines can be tailored with precision to integrate with PROTACs which hold significant potential to facilitate PROTAC nanomedicines (nano-PROTACs) for clinical translation with enhanced efficacy and reduced side effects. In this review, we provide an overview of the recent progress in the convergence of nanotechnology with PROTAC design, leveraging the inherent properties of nanomaterials, such as lipids, polymers, inorganic nanoparticles, nanohydrogels, proteins, and nucleic acids, for precise PROTAC delivery. Additionally, we discuss the various categories of PROTAC targets and provide insights into their clinical translational potential, alongside the challenges that need to be addressed.
引用
收藏
页码:28502 / 28530
页数:29
相关论文
共 50 条
  • [21] BET protein proteolysis targeting chimera (PROTAC) exerts potent lethal activity against mantle cell lymphoma cells
    B Sun
    W Fiskus
    Y Qian
    K Rajapakshe
    K Raina
    K G Coleman
    A P Crew
    A Shen
    D T Saenz
    C P Mill
    A J Nowak
    N Jain
    L Zhang
    M Wang
    J D Khoury
    C Coarfa
    C M Crews
    K N Bhalla
    Leukemia, 2018, 32 : 343 - 352
  • [22] BET protein proteolysis targeting chimera (PROTAC) exerts potent lethal activity against mantle cell lymphoma cells
    Sun, B.
    Fiskus, W.
    Qian, Y.
    Rajapakshe, K.
    Raina, K.
    Coleman, K. G.
    Crew, A. P.
    Shen, A.
    Saenz, D. T.
    Mill, C. P.
    Nowak, A. J.
    Jain, N.
    Zhang, L.
    Wang, M.
    Khoury, J. D.
    Coarfa, C.
    Crews, C. M.
    Bhalla, K. N.
    LEUKEMIA, 2018, 32 (02) : 343 - 352
  • [23] Proteolysis Targeting Chimera (PROTAC) as a promising novel therapeutic modality for the treatment of triple-negative breast cancer (TNBC)
    Dogheim, Gaidaa M.
    Amralla, Mohamed T.
    DRUG DEVELOPMENT RESEARCH, 2023, 84 (04) : 629 - 653
  • [24] Discovery of A031 as effective proteolysis targeting chimera (PROTAC) androgen receptor (AR) degrader for the treatment of prostate cancer
    Chen, Linrong
    Han, Liuquan
    Mao, Shujun
    Xu, Ping
    Xu, Xinxin
    Zhao, Ruibo
    Wu, Zhihua
    Zhong, Kai
    Yu, Guangliang
    Wang, Xiaolei
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2021, 216
  • [25] Proteolysis Targeting Chimera (PROTAC): A Paradigm-Shifting Approach in Small Molecule Drug Discovery
    Wang, Pingyuan
    Zhou, Jia
    CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2018, 18 (16) : 1354 - 1356
  • [26] Selective CDK9 degradation using a proteolysis-targeting chimera (PROTAC) strategy
    Mallareddy, Jayapal Reddy
    Singh, Sarbjit
    Boghean, Lidia
    Natarajan, Amarnath
    FUTURE MEDICINAL CHEMISTRY, 2022, 14 (03) : 131 - 134
  • [27] Discovery of potent epidermal growth factor receptor (EGFR) degraders by proteolysis targeting chimera (PROTAC)
    Zhang, Hao
    Zhao, Hong-Yi
    Xi, Xiao-Xiao
    Liu, Yan-Jie
    Xin, Minhang
    Mao, Shuai
    Zhang, Jun-Jie
    Lu, A-Xin
    Zhang, San-Qi
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2020, 189
  • [28] Proteolysis-Targeting Chimera (PROTAC) Delivery into the Brain across the Blood-Brain Barrier
    Tashima, Toshihiko
    ANTIBODIES, 2023, 12 (03)
  • [29] Discovery of a potent and selective proteolysis targeting chimera (PROTAC) degrader of NSD3 histone methyltransferase
    Sun, Yaoliang
    Zhang, Ying
    Chen, Xiaoai
    Yu, Aisong
    Du, Wenhao
    Huang, Yuting
    Wu, Feifei
    Yu, Lei
    Li, Jiayi
    Wen, Cuiyun
    Yang, Hong
    Shi, Qiongyu
    Geng, Meiyu
    Huang, Xun
    Xu, Shilin
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2022, 239
  • [30] Discovery of ARD-69 as a Highly Potent Proteolysis Targeting Chimera (PROTAC) Degrader of Androgen Receptor (AR) for the Treatment of Prostate Cancer
    Han, Xin
    Wang, Chao
    Qin, Chong
    Xiang, Weiguo
    Fernandez-Salas, Ester
    Yang, Chao-Yie
    Wang, Mi
    Zhao, Lijie
    Xu, Tianfeng
    Chinnaswamy, Krishnapriya
    Delproposto, James
    Stuckey, Jeanne
    Wang, Shaomeng
    JOURNAL OF MEDICINAL CHEMISTRY, 2019, 62 (02) : 941 - 964