siRNA Therapeutics for the Therapy of COVID-19 and Other Coronaviruses

被引:33
作者
Sajid, Muhammad Imran [1 ,2 ]
Moazzam, Muhammad [2 ]
Cho, Yeseom [1 ,3 ]
Kato, Shun [1 ,3 ]
Xu, Ava [1 ]
Way, J. J. [1 ]
Lohan, Sandeep [1 ]
Tiwari, Rakesh K. [1 ]
机构
[1] Chapman Univ, Ctr Targeted Drug Delivery, Dept Biomed & Pharmaceut Sci, Sch Pharm, Irvine, CA 92618 USA
[2] Univ Cent Punjab, Fac Pharm, Lahore 54700, Pakistan
[3] Chapman Univ, Schmid Coll Sci & Technol, Dept Biochem & Mol Biol, Orange, CA 92866 USA
关键词
COVID-19; coronaviruses; dsRNA; nucleic acid therapy; patents; SARS-CoV-2; siRNA delivery; siRNA therapy; HEPATITIS-B-VIRUS; RNA-MEDIATED INHIBITION; SMALL INTERFERING RNAS; SARS-COV REPLICATION; DOUBLE-STRANDED-RNA; GENE-EXPRESSION; SPIKE PROTEIN; SARS-COV-2; IDENTIFICATION; INFECTION;
D O I
10.1021/acs.molpharmaceut.0c01239
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
The ongoing pandemic of global concern has killed about three million humans and affected around 151 million people worldwide, as of April 30, 2021. Although recently approved vaccines for COVID-19 are engendering hope, finding new ways to cure the viral pandemic is still a quest for researchers worldwide. Major pandemics in history have been of viral origin, such as SARS, MERS, H1NI, Spanish flu, and so on. A larger emphasis has been on discovering potential vaccines, novel antiviral drugs, and agents that can mitigate the viral infection symptoms; however, a relatively new area, RNA interference (RNAi), has proven effective as an antiviral agent. The RNAi phenomenon has been largely exploited to cure cancer, neuro-degenerative diseases, and some rare diseases. The U.S. Food and Drug Administration has recently approved three siRNA products for human use that garner significant hope in siRNA therapeutics for coronaviruses. There have been some commentaries and communications addressing this area. We have summarized and illustrated the significance and the potential of the siRNA therapeutics available as of April 30, 2021 to combat the ongoing viral pandemic and the emerging new variants such as B.1.1.7 and B.1.351. Numerous successful in vitro studies and several investigations to address the clinical application of siRNA therapeutics provide great hope in this field. This seminal Review describes the significance of siRNA-based therapy to treat diverse viral infections in addition to the current coronavirus challenge. In addition, we have thoroughly reviewed the patents approved for coronaviruses, the major challenges in siRNA therapy, and the potential approaches to address them, followed by innovation and prospects.
引用
收藏
页码:2105 / 2121
页数:17
相关论文
共 176 条
  • [1] Inhibition of SARS-CoV replication cycle by small interference RNAs silencing specific SARS proteins, 7a/7b, 3a/3b and S
    Akerstrom, Sara
    Mirazimi, Ali
    Tan, Yee-Joo
    [J]. ANTIVIRAL RESEARCH, 2007, 73 (03) : 219 - 227
  • [2] Alnylam Pharmaceuticals, 2020, BIOSPACE
  • [3] RNA silencing of rotavirus gene expression
    Arias, CF
    Dector, MA
    Segovia, L
    López, T
    Camacho, M
    Isa, P
    Espinosa, R
    López, S
    [J]. VIRUS RESEARCH, 2004, 102 (01) : 43 - 51
  • [4] Potential use of noncoding RNAs and innovative therapeutic strategies to target the 5'UTR of SARS-CoV-2
    Baldassarre, Antonella
    Paolini, Alessandro
    Bruno, Stefania Paola
    Felli, Cristina
    Tozzi, Alberto Eugenio
    Masotti, Andrea
    [J]. EPIGENOMICS, 2020, 12 (15) : 1349 - 1361
  • [5] SARS-CoV-2 Disrupts Splicing, Translation, and Protein Trafficking to Suppress Host Defenses
    Banerjee, Abhik K.
    Blanco, Mario R.
    Bruce, Emily A.
    Honson, Drew D.
    Chen, Linlin M.
    Chow, Amy
    Bhat, Prashant
    Ollikainen, Noah
    Quinodoz, Sofia A.
    Loney, Colin
    Thai, Jasmine
    Miller, Zachary D.
    Lin, Aaron E.
    Schmidt, Madaline M.
    Stewart, Douglas G.
    Goldfarb, Daniel
    De Lorenzo, Giuditta
    Rihn, Suzannah J.
    Voorhees, Rebecca M.
    Botten, Jason W.
    Majumdar, Devdoot
    Guttman, Mitchell
    [J]. CELL, 2020, 183 (05) : 1325 - +
  • [6] Short interfering RNA-mediated inhibition of herpes simplex virus type 1 gene expression and function during infection of human keratinocytes
    Bhuyan, PK
    Karikò, K
    Capodici, J
    Lubinski, J
    Hook, LM
    Friedman, HM
    Weissman, D
    [J]. JOURNAL OF VIROLOGY, 2004, 78 (19) : 10276 - 10281
  • [7] Phenotypic silencing of cytoplasmic genes using sequence-specific double-stranded short interfering RNA and its application in the reverse genetics of wild type negative-strand RNA viruses
    Bitko V.
    Barik S.
    [J]. BMC Microbiology, 1 (1) : 1 - 11
  • [8] Cathepsin L functionally cleaves the severe acute respiratory syndrome coronavirus class I fusion protein upstream of rather than adjacent to the fusion peptide
    Bosch, Berend Jan
    Bartelink, Willem
    Rottier, Peter J. M.
    [J]. JOURNAL OF VIROLOGY, 2008, 82 (17) : 8887 - 8890
  • [9] A large-scale chemical modification screen identifies design rules to generate siRNAs with high activity, high stability and low toxicity
    Bramsen, Jesper B.
    Laursen, Maria B.
    Nielsen, Anne F.
    Hansen, Thomas B.
    Bus, Claus
    Langkjaer, Niels
    Babu, B. Ravindra
    Hojland, Torben
    Abramov, Mikhail
    Van Aerschot, Arthur
    Odadzic, Dalibor
    Smicius, Romualdas
    Haas, Jens
    Andree, Cordula
    Barman, Jharna
    Wenska, Malgorzata
    Srivastava, Puneet
    Zhou, Chuanzheng
    Honcharenko, Dmytro
    Hess, Simone
    Mueller, Elke
    Bobkov, Georgii V.
    Mikhailov, Sergey N.
    Fava, Eugenio
    Meyer, Thomas F.
    Chattopadhyaya, Jyoti
    Zerial, Marino
    Engels, Joachim W.
    Herdewijn, Piet
    Wengel, Jesper
    Kjems, Jorgen
    [J]. NUCLEIC ACIDS RESEARCH, 2009, 37 (09) : 2867 - 2881
  • [10] Specific inhibition of gene expression by small double-stranded RNAs in invertebrate and vertebrate systems
    Caplen, NJ
    Parrish, S
    Imani, F
    Fire, A
    Morgan, RA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (17) : 9742 - 9747