Evidence map›Paper›PMID 36139546›Full record

ReviewCancers2022

Development and Challenges of Diclofenac-Based Novel Therapeutics: Targeting Cancer and Complex Diseases.

Ayeman Amanullah, Arun Upadhyay, Rohan Dhiman, Sarika Singh, Amit Kumar, Dinesh Kumar Ahirwar, Ravi Kumar Gutti, Amit Mishra

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

21 citing papers in PubMed, 51 citations in OpenAlex.

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  20. Microglia as a cellular target of diclofenac therapy in Alzheimer's disease.Therapeutic advances in neurological disorders · 2023
    Review
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

8 authors at 5 institutions in 1 country.

Ayeman AmanullahCellular and Molecular Neurobiology Unit, Indian Institute of Technology Jodhpur, Jodhpur 342037, India.ORCID 0000-0001-8782-1298
Arun UpadhyayCellular and Molecular Neurobiology Unit, Indian Institute of Technology Jodhpur, Jodhpur 342037, India.ORCID 0000-0002-3216-1277
Rohan DhimanLaboratory of Mycobacterial Immunology, Department of Life Science, National Institute of Technology, Rourkela 769008, India.
Sarika SinghDivision of Toxicology and Experimental Medicine, Department of Neuroscience and Ageing Biology, CSIR-Central Drug Research Institute, Lucknow 226031, India.
Amit KumarDepartment of Biosciences and Biomedical Engineering, Indian Institute of Technology Indore, Simrol, Indore 453552, India.
Dinesh Kumar AhirwarTumor Microenvironment Unit, Department of Bioscience & Bioengineering, Indian Institute of Technology Jodhpur, Jodhpur 342037, India.
Ravi Kumar GuttiDepartment of Biochemistry, University of Hyderabad, Hyderabad 500046, India.ORCID 0000-0002-0912-5796
Amit MishraCellular and Molecular Neurobiology Unit, Indian Institute of Technology Jodhpur, Jodhpur 342037, India.ORCID 0000-0001-9401-4400
Indian Institute of Technology Jodhpur · INCentral Drug Research Institute · INIndian Institute of Technology Indore · INNational Institute of Technology Rourkela · INUniversity of Hyderabad · IN

Funding

Science and Engineering Research Board EMR/2016/000716
6 · The paper itself

Abstract

Diclofenac is a highly prescribed non-steroidal anti-inflammatory drug (NSAID) that relieves inflammation, pain, fever, and aches, used at different doses depending on clinical conditions. This drug inhibits cyclooxygenase-1 and cyclooxygenase-2 enzymes, which are responsible for the generation of prostaglandin synthesis. To improve current diclofenac-based therapies, we require new molecular systematic therapeutic approaches to reduce complex multifactorial effects. However, the critical challenge that appears with diclofenac and other drugs of the same class is their side effects, such as signs of stomach injuries, kidney problems, cardiovascular issues, hepatic issues, and diarrhea. In this article, we discuss why defining diclofenac-based mechanisms, pharmacological features, and its medicinal properties are needed to direct future drug development against neurodegeneration and imperfect ageing and to improve cancer therapy. In addition, we describe various advance molecular mechanisms and fundamental aspects linked with diclofenac which can strengthen and enable the better designing of new derivatives of diclofenac to overcome critical challenges and improve their applications.

Indexed as

ageingcancerCOXdiclofenacneurodegenerationNSAIDs

Identifiers

PMID36139546
PMCPMC9496891
OpenAlexW4295211186

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.