Evidence map›Paper›PMID 34445373›Full record

ReviewInternational journal of molecular sciences2021

SARS-CoV-2: Understanding the Transcriptional Regulation of ACE2 and TMPRSS2 and the Role of Single Nucleotide Polymorphism (SNP) at Codon 72 of p53 in the Innate Immune Response against Virus Infection.

Niraj Lodhi, Rubi Singh, Satya Prakash Rajput, Quaiser Saquib

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. NAR cancer · 2023
    Article
  6. p53 and Myofibroblast Apoptosis in Organ Fibrosis.International journal of molecular sciences · 2023
    Review
  7. Review
  8. Allelic Variations in the Human GenesInternational journal of molecular sciences · 2022
    Article
  9. Article
  10. Article
  11. Frontiers in pharmacology · 2022
    Article
  12. Review
  13. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 4 institutions in 3 countries.

Niraj LodhiClinical Research (Research and Development Division) miRNA Analytics LLC, Harlem Bio-Space, New York, NY 10027, USA.ORCID 0000-0002-5940-2915
Rubi SinghDepartment of Pharmacology, Weill Cornell Medicine, New York, NY 10065, USA.
Satya Prakash RajputSchool of Life Sciences, Warwick University, Coventry CV47AL, UK.
Quaiser SaquibDepartment of Zoology, College of Sciences, King Saud University, Riyadh 12372, Saudi Arabia.ORCID 0000-0001-7030-3777
Cornell University · USHarlem United · USKing Saud University · SAUniversity of Warwick · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human ACE2 and the serine protease TMPRSS2 of novel SARS-CoV-2 are primary entry receptors in host cells. Expression of these genes at the transcriptional level has not been much discussed in detail. The ISRE elements of the ACE2 promoter are a binding site for the ISGF3 complex of the JAK/STAT signaling pathway. TMPRSS2, including IFNβ, STAT1, and STAT2, has the PARP1 binding site near to TSS either up or downstream promoter region. It is well documented that PARP1 regulates gene expression at the transcription level. Therefore, to curb virus infection, both promoting type I IFN signaling to boost innate immunity and prevention of virus entry by inhibiting PARP1, ACE2 or TMPRSS2 are safe options. Most importantly, our aim is to attract the attention of the global scientific community towards the codon 72 Single Nucleotide Polymorphism (SNP) of p53 and its underneath role in the innate immune response against SARS-CoV-2. Here, we discuss codon 72 SNP of human p53's role in the different innate immune response to restrict virus-mediated mortality rate only in specific parts of the world. In addition, we discuss potential targets and emerging therapies using bioengineered bacteriophage, anti-sense, or CRISPR strategies.

Indexed as

Angiotensin-Converting Enzyme 2Binding SitesCOVID-19HumansImmunity, InnatePoly (ADP-Ribose) Polymerase-1Polymorphism, Single NucleotideSARS-CoV-2Serine EndopeptidasesVaccinationVirus InternalizationACE2 protein, humanAngiotensin-Converting Enzyme 2PARP1 protein, humanPoly (ADP-Ribose) Polymerase-1Serine EndopeptidasesTMPRSS2 protein, humanACE2codon 72 polymorphism of p53innate immune responseinterferonp53PARP1SARS-CoV-2Single Nucleotide Polymorphism (SNP)TLRs (toll-like receptors)TMPRSS2transcription

Identifiers

PMID34445373
PMCPMC8395432
OpenAlexW3187596458

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.