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1.
Mol Biol Rep ; 49(6): 4943-4957, 2022 Jun.
Article in English | MEDLINE | ID: mdl-35235159

ABSTRACT

The world is grappling with an unprecedented public health crisis COVID-19 pandemic caused by the novel coronavirus SARS-CoV-2. Due to the high transmission/mortality rates and socioeconomic impacts of the COVID-19, its control is crucial. In the absence of specific treatment, vaccines represent the most efficient way to control and stop the pandemic. Many companies around the world are currently making efforts to develop the vaccine to combat COVID-19. This review outlines key strategies for generating SARS-CoV-2 vaccine candidates, along with the mechanism of action, advantages, and potential limitations of each vaccine. The use of nanomaterials and nanotechnology for COVID-19 vaccines development will also be discussed.


Subject(s)
COVID-19 Vaccines , COVID-19 , COVID-19/prevention & control , Humans , Pandemics/prevention & control , SARS-CoV-2
2.
Cancer Invest ; 40(6): 516-543, 2022 Jul.
Article in English | MEDLINE | ID: mdl-35320055

ABSTRACT

Anti-metabolite drugs prevent the synthesis of essential cell growth compounds. 5-fluorouracil is used as an anti-metabolic drug in various cancers in the first stage of treatment. Unfortunately, in some cancers, 5-fluorouracil has low effectiveness because of its drug resistance. Studies have shown that drug resistance to 5-fluorouracil is due to the activation of specific signaling pathways and increased expressions of enzymes involved in drug metabolites. However, when 5-fluorouracil is used in combination with other drugs, the sensitivity of cancer cells to 5-fluorouracil increases, and the effect of drug resistance is reversed. This study discusses how the function of 5-fluorouracil in JAK/STAT, Wnt, Notch, NF-κB, and hedgehogs in some cancers.


Subject(s)
Apoptosis , Neoplasms , Cell Line, Tumor , Drug Resistance , Drug Resistance, Neoplasm , Fluorouracil/pharmacology , Fluorouracil/therapeutic use , Humans , NF-kappa B/metabolism , Neoplasms/drug therapy , Signal Transduction
3.
Eur J Med Res ; 27(1): 6, 2022 Jan 13.
Article in English | MEDLINE | ID: mdl-35027080

ABSTRACT

SARS-CoV-2, a novel coronavirus, is the agent responsible for the COVID-19 pandemic and is a major public health concern nowadays. The rapid and global spread of this coronavirus leads to an increase in hospitalizations and thousands of deaths in many countries. To date, great efforts have been made worldwide for the efficient management of this crisis, but there is still no effective and specific treatment for COVID-19. The primary therapies to treat the disease are antivirals, anti-inflammatories and respiratory therapy. In addition, antibody therapies currently have been a many active and essential part of SARS-CoV-2 infection treatment. Ongoing trials are proposed different therapeutic options including various drugs, convalescent plasma therapy, monoclonal antibodies, immunoglobulin therapy, and cell therapy. The present study summarized current evidence of these therapeutic approaches to assess their efficacy and safety for COVID-19 treatment. We tried to provide comprehensive information about the available potential therapeutic approaches against COVID-19 to support researchers and physicians in any current and future progress in treating COVID-19 patients.


Subject(s)
COVID-19 Drug Treatment , COVID-19/therapy , Immunization, Passive , Antibodies, Monoclonal/therapeutic use , Antibodies, Neutralizing , Antiviral Agents/therapeutic use , Clinical Trials as Topic , Dietary Supplements , Humans , Immunization, Passive/methods , Immunoglobulins, Intravenous/therapeutic use , Pandemics , SARS-CoV-2 , Treatment Outcome , COVID-19 Serotherapy
4.
Biomed Pharmacother ; 145: 112420, 2022 Jan.
Article in English | MEDLINE | ID: mdl-34801852

ABSTRACT

Deciphering the molecular downstream consequences of severe acute respiratory syndrome coronavirus (SARS-CoV)- 2 infection is important for a greater understanding of the disease and treatment planning. Furthermore, greater understanding of the underlying mechanisms of diagnostic and therapeutic strategies can help in the development of vaccines and drugs against COVID-19. At present, the molecular mechanisms of SARS-CoV-2 in the host cells are not sufficiently comprehended. Some of the mechanisms are proposed considering the existing similarities between SARS-CoV-2 and the other members of the ß-CoVs, and others are explained based on studies advanced in the structure and function of SARS-CoV-2. In this review, we endeavored to map the possible mechanisms of the host response following SARS-CoV-2 infection and surveyed current research conducted by in vitro, in vivo and human observations, as well as existing suggestions. We addressed the specific signaling events that can cause cytokine storm and demonstrated three forms of cell death signaling following virus infection, including apoptosis, pyroptosis, and necroptosis. Given the elicited signaling pathways, we introduced possible pathway-based therapeutic targets; ADAM17 was especially highlighted as one of the most important elements of several signaling pathways involved in the immunopathogenesis of COVID-19. We also provided the possible drug candidates against these targets. Moreover, the cytokine-cytokine receptor interaction pathway was found as one of the important cross-talk pathways through a pathway-pathway interaction analysis for SARS-CoV-2 infection.


Subject(s)
COVID-19 Drug Treatment , COVID-19 , Host-Pathogen Interactions , Molecular Targeted Therapy/methods , SARS-CoV-2/physiology , Signal Transduction/drug effects , COVID-19/immunology , COVID-19/virology , Drug Discovery , Host-Pathogen Interactions/drug effects , Host-Pathogen Interactions/immunology , Humans
5.
Gene ; 730: 144323, 2020 Mar 10.
Article in English | MEDLINE | ID: mdl-31917230

ABSTRACT

The subjection of DNA to numerous lethal damages is threatening for the stability and integrity of the whole body genome. DNA damage response (DDR) is a critical phosphorylation-based signaling pathway developed for the maintaining of the genome against these threatens. Recent studies showed that various targets of DDR are involved in the activation of autophagy, as one of the important effectors of this signaling. The interplay between DDR and autophagy may have a critical role in the pathogenesis of various malignancies such as colorectal cancer, which can be a basement for the designing novel therapeutic strategies for combating this cancer type. On the other hand, autophagy is also demonstrated to be contributed to the regulation of DDR components. Therefore, in this review article, we will discuss the crosstalk between DDR and autophagy and their exact function in the pathogenesis of various human cancer types, with special attention on colorectal cancer.


Subject(s)
Autophagy/genetics , Colorectal Neoplasms/metabolism , DNA Repair/physiology , Colonic Neoplasms/genetics , Colorectal Neoplasms/genetics , DNA Damage/physiology , Genomic Instability/genetics , Humans , Signal Transduction/genetics
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