RNA therapeutics in targeting G protein-coupled receptors: Recent advances and challenges

被引:2
|
作者
Yuan, Wanjun
Shi, Xiangyang [1 ]
Lee, Leo Tsz On [2 ,3 ,4 ]
机构
[1] Univ Macau, Fac Hlth Sci, Canc Ctr, Taipa 999078, Macau, Peoples R China
[2] Donghua Univ, Coll Biol Sci & Med Engn, Shanghai Engn Res Ctr Nanobiomaterials & Regenerat, State Key Lab Modificat Chem Fibers & Polymer Mat, Shanghai 201620, Peoples R China
[3] Univ Macau, Frontiers Sci Ctr Precis Oncol, Minist Educ, Taipa 999078, Macau, Peoples R China
[4] Univ Macau, Fac Hlth Sci, Frontiers Sci Ctr Precis Oncol, Canc Ctr, Taipa, Macau, Peoples R China
来源
MOLECULAR THERAPY NUCLEIC ACIDS | 2024年 / 35卷 / 02期
关键词
DRUG-DELIVERY SYSTEM; SMALL-ACTIVATING RNA; CELL-PROLIFERATION; SIRNA; CANCER; PEPTIDE; NANOPARTICLES; PHARMACOLOGY; EXPRESSION; MANAGEMENT;
D O I
10.1016/j.omtn.2024.102195
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
G protein -coupled receptors (GPCRs) are the major targets of existing drugs for a plethora of human diseases and dominate the pharmaceutical market. However, over 50% of the GPCRs remain undruggable. To pursue a breakthrough and overcome this situation, there is signi fi cant clinical research for developing RNA -based drugs speci fi cally targeting GPCRs, but none has been approved so far. RNA therapeutics represent a unique and promising approach to selectively targeting previously undruggable targets, including undruggable GPCRs. However, the development of RNA therapeutics faces signi fi - cant challenges in areas of RNA stability and ef fi cient in vivo delivery. This review presents an overview of the advances in RNA therapeutics and the diverse types of nanoparticle RNA delivery systems. It also describes the potential applications of GPCR-targeted RNA drugs for various human diseases.
引用
收藏
页数:24
相关论文
共 50 条
  • [31] Targeting of G protein-coupled receptors to the plasma membrane in health and disease
    Ulloa-Aguirre, Alfredo
    Conn, P. Michael
    FRONTIERS IN BIOSCIENCE-LANDMARK, 2009, 14 : 973 - 994
  • [32] Functional autoantibodies targeting G protein-coupled receptors in rheumatic diseases
    Otavio Cabral-Marques
    Gabriela Riemekasten
    Nature Reviews Rheumatology, 2017, 13 : 648 - 656
  • [33] Targeting G Protein-Coupled Receptors in the Treatment of Parkinson's Disease
    Jones-Tabah, Jace
    JOURNAL OF MOLECULAR BIOLOGY, 2023, 435 (12)
  • [34] Targeting G Protein-Coupled Receptors in Immuno-Oncological Therapies
    Stagg, John
    Gutkind, J. Silvio
    ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2025, 65 : 315 - 331
  • [35] Functional autoantibodies targeting G protein-coupled receptors in rheumatic diseases
    Cabral-Marques, Otavio
    Riemekasten, Gabriela
    NATURE REVIEWS RHEUMATOLOGY, 2017, 13 (11) : 648 - 656
  • [36] Targeting G protein-coupled 7TM receptors in inflammation
    Ulven, Trond
    CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2006, 6 (13) : 1317 - 1318
  • [37] Recent advances in acid sensing by G protein coupled receptors
    Maike D. Glitsch
    Pflügers Archiv - European Journal of Physiology, 2024, 476 : 445 - 455
  • [38] Recent advances in acid sensing by G protein coupled receptors
    Glitsch, Maike D.
    PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2024, 476 (04): : 445 - 455
  • [39] Allosteric modulation of G protein-coupled receptors: perspectives and recent developments
    Soudijn, W
    van Wijngaarden, I
    Ijzerman, AP
    DRUG DISCOVERY TODAY, 2004, 9 (17) : 752 - 758
  • [40] Downregulation of G protein-coupled receptors
    Tsao, P
    von Zastrow, M
    CURRENT OPINION IN NEUROBIOLOGY, 2000, 10 (03) : 365 - 369