COVID-19 signalome: Potential therapeutic interventions

被引:7
作者
Lundstrom, Kenneth [1 ]
Hromic-Jahjefendic, Altijana [2 ]
Bilajac, Esma [2 ,4 ]
Aljabali, Alaa A. A. [3 ]
Baralic, Katarina
Sabri, Nagwa A. [5 ]
Shehata, Eslam M. [6 ]
Raslan, Mohamed [6 ]
Raslan, Sara A. [6 ]
Ferreira, Ana Claudia B. H. [7 ,8 ]
Orlandi, Lidiane [7 ,8 ]
Serrano-Aroca, Angel [9 ]
Uversky, Vladimir N. [10 ]
Hassan, Sk. Sarif [11 ]
Redwan, Elrashdy M. [12 ]
Azevedo, Vasco [13 ]
Alzahrani, Khalid J. [14 ]
Alsharif, Khalaf F. [14 ]
Halawani, Ibrahim F. [14 ]
Alzahrani, Fuad M. [14 ]
Tambuwala, Murtaza M. [15 ]
Barh, Debmalya [13 ,16 ]
机构
[1] PanTherapeutics, Route Lavaux 49, CH-1095 Lutry, Switzerland
[2] Int Univ Sarajevo, Fac Engn & Nat Sci, Dept Genet & Bioengn, Hrasnicka Cesta 15, Sarajevo 71000, Bosnia & Herceg
[3] Yarmouk Univ, Fac Pharm, Dept Pharmaceut & Pharmaceut Technol, POB 566, Irbid 21163, Jordan
[4] Univ Belgrade, Fac Pharm, Dept Toxicol Akad Danilo Soldatovic, Vojvode Stepe 450, Belgrade 11221, Serbia
[5] Ain Shams Univ, Fac Pharm, Dept Clin Pharm, Cairo 11865, Egypt
[6] Drug Res Ctr, Clin Res & Bioanal Dept, Cairo 11865, Egypt
[7] Univ Estadual Campinas, Campinas, SP, Brazil
[8] Univ Ctr Lavras UNILAVRAS, Lavras, MG, Brazil
[9] Univ Catolica Valencia San Vicente Martir, Ctr Invest Traslac San Alberto Magno, Biomat & Bioengn Lab, C Guillem Castro 94, Valencia 46001, Spain
[10] Univ S Florida, USF Hlth Byrd Alzheimers Inst, Morsani Coll Med, Dept Mol Med, Tampa, FL 33612 USA
[11] Pingla Thana Mahavidyalaya, Dept Math, Maligram 721140, India
[12] King Abdulaziz Univ, Fac Sci, Dept Biol Sci, POB 80203, Jeddah, Saudi Arabia
[13] Univ Fed Minas Gerais, Inst Biol Sci, Dept Genet Ecol & Evolut, BR-31270901 Belo Horizonte, MG, Brazil
[14] Taif Univ, Coll Appl Med Sci, Dept Clin Labs Sci, POB 11099, Taif 11099, Saudi Arabia
[15] Univ Lincoln, Lincoln Med Sch, Brayford Pool Campus, Lincoln LN6 7TS, England
[16] Inst Integrat Omics & Appl Biotechnol IIOAB, Purba Medinipur 721172, India
基金
英国科研创新办公室;
关键词
SARS-CoV-2; COVID-19; Signalome; Antiviral drugs; Vaccines; Signaling pathways; ACUTE RESPIRATORY SYNDROME; RENIN-ANGIOTENSIN SYSTEM; SARS CORONAVIRUS; CELL ENTRY; SARS-COV-2; INHIBITORS; PROTEIN; ACE2; RECEPTOR; VIRUS;
D O I
10.1016/j.cellsig.2022.110559
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The COVID-19 pandemic has triggered intensive research and development of drugs and vaccines against SARS-CoV-2 during the last two years. The major success was especially observed with development of vaccines based on viral vectors, nucleic acids and whole viral particles, which have received emergent authorization leading to global mass vaccinations. Although the vaccine programs have made a big impact on COVID-19 spread and severity, emerging novel variants have raised serious concerns about vaccine efficacy. Due to the urgent demand, drug development had originally to rely on repurposing of antiviral drugs developed against other infectious diseases. For both drug and vaccine development the focus has been mainly on SARS-CoV-2 surface proteins and host cell receptors involved in viral attachment and entry. In this review, we expand the spectrum of SARS-CoV-2 targets by investigating the COVID-19 signalome. In addition to the SARS-CoV-2 Spike protein, the envelope, membrane, and nucleoprotein targets have been subjected to research. Moreover, viral proteases have presented the possibility to develop different strategies for the inhibition of SARS-CoV-2 replication and spread. Several signaling pathways involving the renin-angiotensin system, angiotensin-converting enzymes, immune pathways, hypoxia, and calcium signaling have provided attractive alternative targets for more efficient drug development.
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页数:14
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