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  1. Article ; Online: Antigenic sites in SARS-CoV-2 spike RBD show molecular similarity with pathogenic antigenic determinants and harbors peptides for vaccine development.

    Dakal, Tikam Chand

    Immunobiology

    2021  Volume 226, Issue 5, Page(s) 152091

    Abstract: The spike protein of coronavirus is key target for drug development and other pharmacological interventions. In current study, we performed an integrative approach to predict antigenic sites in SARS-CoV-2 spike receptor binding domain and found nine ... ...

    Abstract The spike protein of coronavirus is key target for drug development and other pharmacological interventions. In current study, we performed an integrative approach to predict antigenic sites in SARS-CoV-2 spike receptor binding domain and found nine potential antigenic sites. The predicted antigenic sites were then assessed for possible molecular similarity with other known antigens in different organisms. Out of nine sites, seven sites showed molecular similarity with 54 antigenic determinants found in twelve pathogenic bacterial species (Mycobacterium tuberculosis, Mycobacterium leprae, Bacillus anthracis, Borrelia burgdorferi, Clostridium perfringens, Clostridium tetani, Helicobacter Pylori, Listeria monocytogenes, Staphylococcus aureus, Streptococcus pyogenes, Vibrio cholera and Yersinia pestis), two malarial parasites (Plasmodium falciparum and Plasmodium knowlesi) and influenza virus A. Most of the bacterial antigens that displayed molecular similarity with antigenic sites in SARS-CoV-2 RBD (receptor binding domain) were toxins and virulent factors. Antigens from Mycobacterium that showed similarity were mainly involved in modulating host cell immune response and ensuring persistence and survival of pathogen in host cells. Presence of a large number of antigenic determinants, similar to those in highly pathogenic microorganisms, not merely accounts for complex etiology of the disease but also provides an explanation for observed pathophysiological complications, such as deregulated immune response, unleashed or dysregulated cytokine secretion (cytokine storm), multiple organ failure etc., that are more evident in aged and immune-compromised patients. Over-representation of antigenic determinants from Plasmodium and Mycobacterium in all antigenic sites suggests that anti-malarial and anti-TB drugs can prove to be clinical beneficial for COVID-19 treatment. Besides this, anti-leprosy, anti-lyme, anti-plague, anti-anthrax drugs/vaccine etc. are also expected to be beneficial in COVID-19 treatment. Moreover, individuals previously immunized/vaccinated or had previous history of malaria, tuberculosis or other disease caused by fifteen microorganisms are expected to display a considerable degree of resistance against SARS-CoV-2 infection. Out of the seven antigenic sites predicted in SARS-CoV-2, a part of two antigenic sites were also predicted as potent T-cell epitopes (KVGGNYNYL
    MeSH term(s) Antigens, Viral/immunology ; Bacteria/immunology ; Binding Sites ; COVID-19/prevention & control ; COVID-19 Vaccines ; Epitopes, T-Lymphocyte/immunology ; Influenza A virus/immunology ; Peptides/immunology ; Plasmodium/immunology ; Protein Domains ; SARS-CoV-2/immunology ; Spike Glycoprotein, Coronavirus/immunology
    Chemical Substances Antigens, Viral ; COVID-19 Vaccines ; Epitopes, T-Lymphocyte ; Peptides ; Spike Glycoprotein, Coronavirus ; spike protein, SARS-CoV-2
    Language English
    Publishing date 2021-07-13
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 563292-4
    ISSN 1878-3279 ; 0171-2985
    ISSN (online) 1878-3279
    ISSN 0171-2985
    DOI 10.1016/j.imbio.2021.152091
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: SARS-CoV-2 attachment to host cells is possibly mediated via RGD-integrin interaction in a calcium-dependent manner and suggests pulmonary EDTA chelation therapy as a novel treatment for COVID 19.

    Dakal, Tikam Chand

    Immunobiology

    2020  Volume 226, Issue 1, Page(s) 152021

    Abstract: SARS-CoV-2 is a highly contagious virus that has caused serious health crisis world-wide resulting into a pandemic situation. As per the literature, the SARS-CoV-2 is known to exploit humanACE2 receptors (similar toprevious SARS-CoV-1) for gaining entry ... ...

    Abstract SARS-CoV-2 is a highly contagious virus that has caused serious health crisis world-wide resulting into a pandemic situation. As per the literature, the SARS-CoV-2 is known to exploit humanACE2 receptors (similar toprevious SARS-CoV-1) for gaining entry into the host cell for invasion, infection, multiplication and pathogenesis. However, considering the higher infectivity of SARS-CoV-2 along with the complex etiology and pathophysiological outcomes seen in COVID-19 patients, it seems that there may be an alternate receptor for SARS-CoV-2. I performed comparative protein sequence analysis, database based gene expression profiling, bioinformatics based molecular docking using authentic tools and techniques for unveiling the molecular basis of high infectivity of SARS-CoV-2 as compared to previous known coronaviruses. My study revealed that SARS-CoV-2 (previously known as 2019-nCoV) harbors a RGD motif in its receptor binding domain (RBD) and the motif is absent in all other previously known SARS-CoVs. The RGD motif is well known for its role in cell-attachment and cell-adhesion. My hypothesis is that the SARS-CoV-2 may be (via RGD) exploiting integrins, that have high expression in lungs and all other vital organs, for invading host cells. However, an experimental verification is required. The expression of ACE2, which is a known receptor for SARS-CoV-2, was found to be negligible in lungs. I assume that higher infectivity of SARS-CoV-2 could be due to this RGD-integrin mediated acquired cell-adhesive property. Gene expression profiling revealed that expression of integrins is significantly high in lung cells, in particular αvβ6, α5β1, αvβ8 and an ECM protein, ICAM1. The molecular docking experiment showed the RBD of spike protein binds with integrins precisely at RGD motif in a similar manner as a synthetic RGD peptide binds to integrins as found by other researchers. SARS-CoV-2 spike protein has a number of phosphorylation sites that can induce cAMP, PKC, Tyr signaling pathways. These pathways either activate calcium ion channels or get activated by calcium. In fact, integrins have calcium & metal binding sites that were predicted around and in vicinity of RGD-integrin docking site in our analysis which suggests that RGD-integrins interaction possibly occurs in calcium-dependent manner. The higher expression of integrins in lungs along with their previously known high binding affinity (~K
    MeSH term(s) Angiotensin-Converting Enzyme 2/metabolism ; Binding Sites/genetics ; COVID-19/virology ; Calcium/metabolism ; Calcium Channels/metabolism ; Chelation Therapy ; Edetic Acid/therapeutic use ; Gene Expression Profiling ; Humans ; Integrins/chemistry ; Integrins/metabolism ; Intercellular Adhesion Molecule-1/metabolism ; Interleukin-6/metabolism ; Lung/metabolism ; Molecular Docking Simulation ; Oligopeptides/chemistry ; Oligopeptides/metabolism ; Protein Binding ; Receptors, Immunologic/metabolism ; Receptors, Peptide/metabolism ; Receptors, Virus/metabolism ; SARS-CoV-2/metabolism ; SARS-CoV-2/pathogenicity ; Sequence Alignment ; Signal Transduction/genetics ; Spike Glycoprotein, Coronavirus/chemistry ; Spike Glycoprotein, Coronavirus/genetics ; Spike Glycoprotein, Coronavirus/metabolism ; Tumor Necrosis Factor-alpha/metabolism ; Virus Attachment ; COVID-19 Drug Treatment
    Chemical Substances Calcium Channels ; ICAM1 protein, human ; IL6 protein, human ; Integrins ; Interleukin-6 ; Oligopeptides ; Receptors, Immunologic ; Receptors, Peptide ; Receptors, Virus ; Spike Glycoprotein, Coronavirus ; Tumor Necrosis Factor-alpha ; arginyl-glycyl-aspartic acid directed cell adhesion receptor ; spike glycoprotein, SARS-CoV ; spike protein, SARS-CoV-2 ; Intercellular Adhesion Molecule-1 (126547-89-5) ; arginyl-glycyl-aspartic acid (78VO7F77PN) ; Edetic Acid (9G34HU7RV0) ; ACE2 protein, human (EC 3.4.17.23) ; Angiotensin-Converting Enzyme 2 (EC 3.4.17.23) ; Calcium (SY7Q814VUP)
    Language English
    Publishing date 2020-11-05
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 563292-4
    ISSN 1878-3279 ; 0171-2985
    ISSN (online) 1878-3279
    ISSN 0171-2985
    DOI 10.1016/j.imbio.2020.152021
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: CircRNA-miRNA-mRNA interactome analysis in endometrial cancer.

    Dakal, Tikam Chand / Kumar, Abhishek / Maurya, Pawan Kumar

    Journal of biomolecular structure & dynamics

    2023  , Page(s) 1–12

    Abstract: In recent years, exploring the potential of miRNAs as novel diagnostic, prognostic and diagnostic markers have gained much attention. In current study, we conducted an in-depth circRNA-miRNA-mRNA interactome to reveal significant molecular processes and ... ...

    Abstract In recent years, exploring the potential of miRNAs as novel diagnostic, prognostic and diagnostic markers have gained much attention. In current study, we conducted an in-depth circRNA-miRNA-mRNA interactome to reveal significant molecular processes and biological pathways putatively associated with endometrial cancer (EC). Firstly, we retrieved two circRNAs from circad, hsa_circ_0002577 & hsa_circ_0109046, based on their association with the EC. Subsequently, we predicted miRNAs sponging sites in the two circRNAs and the potential target mRNAs of the predicted miRNAs. Sequestered miRNAs target a number of oncogenes (CBL, MET, KRAS), tumor suppressor (CFT R), receptor protein kinases & GT Pase (MET, KRAS, RAB1B), methyltransferases (SET D8), receptors associated factors (T RAF2, GRB2), growth factors (FGF20), autophagy (BECN1, AT G14), apoptotic regulators (BCL2), transcription factors (T Fs) (CREB1, RUNX1, RUNX2) and gene regulators (CCND1, HIF1A); and others, including some novel gene candidates (CREB1, FGF20, IFI27), that have never been implicated in EC earlier. The expression of hsa-miR-433-3p showed significant predictive relevance (Fold Change = 1.8, AUC = 0.736, Mann-Whitney test p-value = 6.1 e- 14) suggesting its predictive relevance in assessing patients' response to chemotherapy. The hsamiR- 188-3p targets autophagic and apoptotic regulators and its upregulation in endometriosis may be used as for the early stage diagnostic purpose. The hsa-miR-502-5p targets SET D8, T RAF2 and others and suggests additional genomic/epigenomic molecular targets for promising therapeutic interventions in EC. Predicted miRNAs target a number of mRNAs having varied functional impacts and offer an in-depth mechanistic insights for expatiating the biological and regulatory role in EC.Communicated by Ramaswamy H. Sarma.
    Language English
    Publishing date 2023-12-12
    Publishing country England
    Document type Journal Article
    ZDB-ID 49157-3
    ISSN 1538-0254 ; 0739-1102
    ISSN (online) 1538-0254
    ISSN 0739-1102
    DOI 10.1080/07391102.2023.2291834
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Naringenin Orchestrates and Regulates the Reactive Oxygen Species-Mediated Pathways and Proinflammatory Signaling: Targeting Hallmarks of Aging-Associated Disorders.

    Deepika / Dakal, Tikam Chand / Sharma, Narendra Kumar / Ranga, Vipin / Maurya, Pawan Kumar

    Rejuvenation research

    2024  Volume 27, Issue 1, Page(s) 3–16

    Abstract: The therapeutic application of flavonoids in the management of infectious diseases, cancers, chronic wounds, aging, and neurodegenerative disorders has been well documented in scientific literature. The citric flavonoid naringenin comes under the ... ...

    Abstract The therapeutic application of flavonoids in the management of infectious diseases, cancers, chronic wounds, aging, and neurodegenerative disorders has been well documented in scientific literature. The citric flavonoid naringenin comes under the category of flavanone and exhibits a plethora of health benefits. Very few flavonoids such as curcumin, resveratrol, catechin, quercetin, and kaempferol have been studied to exert their anti-aging properties in humans. The effect of naringenin in the context of age-associated disorders in detail has not been elucidated yet. The databases used for the literature search were Science Direct, Google Scholar, and PubMed. More emphasis has been put on the recent literature on "naringenin" and its effect on "age-associated disorders." Almost all chronic degenerative disorders are characterized by oxidative stress and inflammatory response. The study aims at highlighting the reactive oxygen species-mediated activity of naringenin and the underlying molecular mechanism leading to the prevention of various age-associated disorders. Altogether, the review presents a systematic comprehension of the pharmaceutical and clinicopathological benefits of naringenin in age-associated disorders.
    MeSH term(s) Humans ; Reactive Oxygen Species ; Flavanones/pharmacology ; Flavonoids ; Aging
    Chemical Substances naringenin (HN5425SBF2) ; Reactive Oxygen Species ; Flavanones ; Flavonoids
    Language English
    Publishing date 2024-02-03
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2150779-X
    ISSN 1557-8577 ; 1549-1684
    ISSN (online) 1557-8577
    ISSN 1549-1684
    DOI 10.1089/rej.2023.0065
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: SARS-CoV-2 Attachment to Host Cells is Possibly Mediated via RGD-Integrin Interaction in a Calcium-dependent Manner and Suggests Pulmonary EDTA Chelation Therapy as a Novel Treatment for COVID 19

    Chand Dakal, Tikam

    Immunobiology

    2020  , Page(s) 152021

    Keywords Immunology ; Immunology and Allergy ; Hematology ; covid19
    Language English
    Publisher Elsevier BV
    Publishing country us
    Document type Article ; Online
    ZDB-ID 563292-4
    ISSN 1878-3279 ; 0171-2985
    ISSN (online) 1878-3279
    ISSN 0171-2985
    DOI 10.1016/j.imbio.2020.152021
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  6. Book ; Online: SARS - CoV - 2 Attachment to Host Cells is Possibly Mediated via RGD - Inte grin Interaction in a Calcium - dependent Manner

    DAKAL, TIKAM CHAND

    2020  

    Abstract: Our study revealed that SARS-CoV-2 harbors a RGD motif in its receptor binding domain (RBD) and the motif is absent in all previously known SARS-CoVs. The RGD motif plays a key role in cell-cell adhesion. Integrins display high affinity for RGD motifs ... ...

    Abstract Our study revealed that SARS-CoV-2 harbors a RGD motif in its receptor binding domain (RBD) and the motif is absent in all previously known SARS-CoVs. The RGD motif plays a key role in cell-cell adhesion. Integrins display high affinity for RGD motifs and are known to bind to RGD motifs. Gene expression profiling revealed that expression of integrins is significantly high in lung cells, in particular αvβ6, α5β1, αvβ8 and an ECM protein, ICAM1. However, the expression of ACE2, which is a known receptor for SARS-CoV-2, was found to be negligible. The molecular docking experiment showed the RBD of spike protein binds with integrins precisely at RGD motif in a similar manner as a synthetic RGD peptide binds to integrins as found by other researchers. SARS-CoV-2 spike protein has a number of phosphorylation sites for cAMP, PKC, Tyr signaling pathways. These pathways either activate calcium ion channels or get activated by calcium. In fact, integrins have calcium & metal binding sites that were predicted around and in vicinity of RGD-integrin docking site suggesting RGD-integrins interaction occurs in calcium-dependent manner. The higher expression of integrins in lungs along with their previously known high binding affinity (~KD = 4.0nM) for virus RGD motif could serve as a possible explanation for high infectivity of SARS-CoV-2. On the contrary, the lower expression of human ACE2 in lungs and its low binding affinity (~KD= 15nM) for spike RBD suggests that human ACE2 is less likely to be a receptor for SARS-CoV-2, at least in lung cells. A highly relevant evidence never reported earlier which corroborate in favor of RGD-integrins mediated virus-host attachment is an unleashed cytokine storm which causes due to activation of TNF-α and IL-6 activation; and integrins role in their activation is also well established. Altogether, the current study highlighted the possible role of calcium and other divalent ions in RGD-integrins interaction for virus invasion into host cells and suggested that lowering divalent ion in lungs could avert virus-host cells attachment. Since, EDTA is well known chelating agent, we suggest pulmonary EDTA chelation therapy as a mean to phenotypically remodel the Ca+2 ion concentration in lungs to prevent RGD-integrin interaction which is dependent upon Ca+2 ion for facilitating virus-host cell attachment. The suggested therapy presents a novel, technically simple, quick, safe, affordable and effective solution to prevent SARS-CoV-2 infection and treat COVID 19, especially in the midst of global emergency when a specific treatment is inexistent.
    Keywords covid19
    Publisher Center for Open Science
    Publishing country us
    Document type Book ; Online
    DOI 10.31219/osf.io/chvsa
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  7. Article ; Online: Genetic determinants of lung cancer: Understanding the oncogenic potential of somatic missense mutations.

    Dhakar, Ramgopal / Dakal, Tikam Chand / Sharma, Amit

    Genomics

    2022  Volume 114, Issue 4, Page(s) 110401

    Abstract: Background: Treatment of lung cancer is getting more personalized nowadays and medical practitioners are moving away from conventional histology-driven empirical treatments, platinum-based chemotherapy, and other invasive surgical resections and have ... ...

    Abstract Background: Treatment of lung cancer is getting more personalized nowadays and medical practitioners are moving away from conventional histology-driven empirical treatments, platinum-based chemotherapy, and other invasive surgical resections and have started adopting alternate therapies in which therapeutic targets are patient's molecular oncogenic drivers.
    Aim: The aim of the current study is to extract meaningful information from the online somatic mutation data (retrieved from cBioPortal) of 16 most significantly mutated oncogenes in non-small-cell lung cancer (NSCLC), namely EGFR, NRAS, KRAS, HER2 (ERBB2), RET, MET, ROS1, FGFR1, BRAF, AKT1, MEK1 (MAP2K1), PIK3CA, PTEN, DDR2, LKB1 (STK11) and ALK, for improving our understanding of the pathobiology of the lung cancer that can aid decision-making on critical clinical and therapeutic considerations.
    Methods: Using an integrated approach comprising 4 steps, the oncogenic potential of 661 missense non-synonymous single nucleotide polymorphisms (nsSNPs) in 16 genes was ascertained using 2059 NSCLC (1575 lung adenocarcinomas, 484 lung squamous cell carcinomas) patients' online mutation data. The steps used comprise sequence/structure homology-based prediction, scoring of conservation of mutated residues and positions, prediction of resulting molecular and functional consequences using machine-learning and structure-guided approach.
    Results: Out of a total of 661 nsSNPs analyzed, a set of 29 nsSNPs has been identified as conserved high confidence mutations in 10 of 16 genes relevant to the under study. Out of 29 conserved high confidence nsSNPs, 4 nsSNPs (EGFR N1094Y, BRAF M620I, DDR2 R307L, ALK P1350T) have been found to be putative novel rare genetic markers for NSCLC.
    Conclusions: The current study, the first of its kind, has provided a list of deleterious non-synonymous somatic mutations in a selected pool of oncogenes that can be considered as a promising target for future drug design and therapy for patients with lung adenocarcinomas and squamous cell carcinomas.
    MeSH term(s) Adenocarcinoma of Lung/genetics ; Carcinoma, Non-Small-Cell Lung/drug therapy ; Carcinoma, Squamous Cell/genetics ; ErbB Receptors ; Humans ; Lung Neoplasms/pathology ; Mutation ; Mutation, Missense ; Oncogenes ; Protein-Tyrosine Kinases/genetics ; Protein-Tyrosine Kinases/therapeutic use ; Proto-Oncogene Proteins/genetics ; Proto-Oncogene Proteins/therapeutic use ; Proto-Oncogene Proteins B-raf/genetics ; Proto-Oncogene Proteins B-raf/therapeutic use ; Receptor Protein-Tyrosine Kinases/genetics ; Receptor Protein-Tyrosine Kinases/therapeutic use
    Chemical Substances Proto-Oncogene Proteins ; ErbB Receptors (EC 2.7.10.1) ; Protein-Tyrosine Kinases (EC 2.7.10.1) ; Receptor Protein-Tyrosine Kinases (EC 2.7.10.1) ; Proto-Oncogene Proteins B-raf (EC 2.7.11.1)
    Language English
    Publishing date 2022-06-14
    Publishing country United States
    Document type Journal Article
    ZDB-ID 356334-0
    ISSN 1089-8646 ; 0888-7543
    ISSN (online) 1089-8646
    ISSN 0888-7543
    DOI 10.1016/j.ygeno.2022.110401
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: SARS-CoV-2 Attachment to Host Cells is Possibly Mediated via RGD-Integrin Interaction in a Calcium-dependent Manner and Suggests Pulmonary EDTA Chelation Therapy as a Novel Treatment for COVID 19

    Chand Dakal, Tikam

    Immunobiology

    Abstract: SARS-CoV-2 is a highly contagious virus that has caused serious health crisis world-wide resulting into a pandemic situation As per the literature, the SARS-CoV-2 is known to exploit humanACE2 receptors (similar toprevious SARS-CoV-1) for gaining entry ... ...

    Abstract SARS-CoV-2 is a highly contagious virus that has caused serious health crisis world-wide resulting into a pandemic situation As per the literature, the SARS-CoV-2 is known to exploit humanACE2 receptors (similar toprevious SARS-CoV-1) for gaining entry into the host cell for invasion, infection, multiplication and pathogenesis However, considering the higher infectivity of SARS-CoV-2 along with the complex etiology and pathophysiological outcomes seen in COVID-19 patients, it seems that there may be an alternate receptor for SARS-CoV-2 I performed comparative protein sequence analysis, database based gene expression profiling, bioinformatics based molecular docking using authentic tools and techniques for unveiling the molecular basis of high infectivity of SARS-CoV-2 as compared to previous known coronaviruses My study revealed that SARS-CoV-2 (previously known as 2019-nCoV) harbors a RGD motif in its receptor binding domain (RBD) and the motif is absent in all other previously known SARS-CoVs The RGD motif is well known for its role in cell-attachment and cell-adhesion My hypothesis is that the SARS-CoV-2 may be (via RGD) exploiting integrins, that have high expression in lungs and all other vital organs, for invading host cells However, an experimental verification is required The expression of ACE2, which is a known receptor for SARS-CoV-2, was found to be negligible in lungs I assume that higher infectivity of SARS-CoV-2 could be due to this RGD-integrin mediated acquired cell-adhesive property Gene expression profiling revealed that expression of integrins is significantly high in lung cells, in particular αvβ6, α5β1, αvβ8 and an ECM protein, ICAM1 The molecular docking experiment showed the RBD of spike protein binds with integrins precisely at RGD motif in a similar manner as a synthetic RGD peptide binds to integrins as found by other researchers SARS-CoV-2 spike protein has a number of phosphorylation sites that can induce cAMP, PKC, Tyr signaling pathways These pathways either activate calcium ion channels or get activated by calcium In fact, integrins have calcium & metal binding sites that were predicted around and in vicinity of RGD-integrin docking site in our analysis which suggests that RGD-integrins interaction possibly occurs in calcium-dependent manner The higher expression of integrins in lungs along with their previously known high binding affinity (∼KD = 4 0nM) for virus RGD motif could serve as a possible explanation for high infectivity of SARS-CoV-2 On the contrary, human ACE2 has lower expression in lungs and its high binding affinity (∼KD= 15nM) for spike RBD alone could not manifest significant virus-host attachment This suggests that besides human ACE2, an additional or alternate receptor for SARS-CoV-2 is likely to exist A highly relevant evidence never reported earlier which corroborate in favor of RGD-integrins mediated virus-host attachment is an unleashed cytokine storm which causes due to activation of TNF-α and IL-6 activation;and integrins role in their activation is also well established Altogether, the current study has highlighted possible role of calcium and other divalent ions in RGD-integrins interaction for virus invasion into host cells and suggested that lowering divalent ion in lungs could avert virus-host cells attachment
    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #908903
    Database COVID19

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  9. Article ; Online: A Reappraisal of the Antiviral Properties of and Immune Regulation through Dietary Phytochemicals.

    Thakur, Mony / Singh, Mona / Kumar, Sandeep / Dwivedi, Ved Prakash / Dakal, Tikam Chand / Yadav, Vinod

    ACS pharmacology & translational science

    2023  Volume 6, Issue 11, Page(s) 1600–1615

    Abstract: In the present era of the COVID-19 pandemic, viral infections remain a major cause of morbidity and mortality worldwide. In this day and age, viral infections are rampant and spreading rapidly. Among the most aggressive viral infections are ebola, AIDS ( ... ...

    Abstract In the present era of the COVID-19 pandemic, viral infections remain a major cause of morbidity and mortality worldwide. In this day and age, viral infections are rampant and spreading rapidly. Among the most aggressive viral infections are ebola, AIDS (acquired immunodeficiency syndrome), influenza, and SARS (severe acute respiratory syndrome). Even though there are few treatment options for viral diseases, most of the antiviral therapies are ineffective owing to frequent mutations, the development of more aggressive strains, drug resistance, and possible side effects. Traditionally, herbal remedies have been used by healers, including for dietary and medicinal purposes. Many clinical and scientific studies have demonstrated the therapeutic potential of plant-derived natural compounds. Because of unsafe practices like blood transfusions and organ transplants from infected patients, medical supply contamination. Our antiviral therapies cannot achieve sterile immunity, and we have yet to find a cure for these pernicious infections. Herbs have been shown to improve therapeutic efficacy against a wide variety of viral diseases because of their high concentration of immunomodulatory phytochemicals (both immunoinhibitory and anti-inflammatory). Combined with biotechnology, this folk medicine system can lead to the development of novel antiviral drugs and therapies. In this Review, we will summarize some selected bioactive compounds with probable mechanisms of their antiviral actions, focusing on the immunological axis of these compounds.
    Language English
    Publishing date 2023-10-10
    Publishing country United States
    Document type Journal Article ; Review
    ISSN 2575-9108
    ISSN (online) 2575-9108
    DOI 10.1021/acsptsci.3c00178
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: PKD1L1

    Whitchurch, Jonathan B / Schneider, Sophia / Hilger, Alina C / Köllges, Ricarda / Stegmann, Jil D / Waffenschmidt, Lea / Dyer, Laura / Thiele, Holger / Dhabhai, Bhanupriya / Dakal, Tikam Chand / Müller, Andreas / Norris, Dominic P / Reutter, Heiko M

    Cells

    2024  Volume 13, Issue 2

    Abstract: Besides visceral heterotaxia, ...

    Abstract Besides visceral heterotaxia,
    MeSH term(s) Animals ; Female ; Humans ; Mice ; Pregnancy ; Chylothorax/genetics ; Fetus ; Genetic Diseases, X-Linked ; Hydrops Fetalis ; Membrane Proteins/genetics ; Membrane Proteins/metabolism ; Mice, Knockout
    Chemical Substances Membrane Proteins ; PKD1L1 protein, human
    Language English
    Publishing date 2024-01-12
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2661518-6
    ISSN 2073-4409 ; 2073-4409
    ISSN (online) 2073-4409
    ISSN 2073-4409
    DOI 10.3390/cells13020149
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