Evidence map›Paper›PMID 26604686›Full record

ReviewDrug design, development and therapy2015

The relevance of piroxicam for the prevention and treatment of nonmelanoma skin cancer and its precursors.

Elena Campione, Evelin Jasmine Paternò, Eleonora Candi, Mattia Falconi, Gaetana Costanza, Laura Diluvio, Alessandro Terrinoni, Luca Bianchi, Augusto Orlandi

Open access · goldAbstract readReview
In one paragraph

Review in Drug design, development and therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

24 citing papers in PubMed, 45 citations in OpenAlex.

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  9. Unboxing the molecular modalities of mutagens in cancer.Environmental science and pollution research international · 2022
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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

9 authors at 1 institution in 1 country.

Elena CampioneDepartment of Dermatology, University of Rome "Tor Vergata" Rome, Italy.
Evelin Jasmine PaternòDepartment of Biomedicine and Prevention, University of Rome "Tor Vergata" Rome, Italy.
Eleonora CandiDepartment of Experimental Medicine and Surgery, University of Rome "Tor Vergata" Rome, Italy ; Biochemistry Laboratory IDI-IRCCS, Faculty of Medicine, University of Rome "Tor Vergata" Rome, Italy.
Mattia FalconiDepartment of Biology, University of Rome "Tor Vergata" Rome, Italy.
Gaetana CostanzaDepartment of Biomedicine and Prevention, University of Rome "Tor Vergata" Rome, Italy.
Laura DiluvioDepartment of Dermatology, University of Rome "Tor Vergata" Rome, Italy.
Alessandro TerrinoniBiochemistry Laboratory IDI-IRCCS, Faculty of Medicine, University of Rome "Tor Vergata" Rome, Italy.
Luca BianchiDepartment of Dermatology, University of Rome "Tor Vergata" Rome, Italy.
Augusto OrlandiDepartment of Biomedicine and Prevention, University of Rome "Tor Vergata" Rome, Italy ; Institute of Anatomic Pathology, University of Rome "Tor Vergata" Rome, Italy ; Tor Vergata University-Policlinic of Rome, Rome, Italy.
University of Rome Tor Vergata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Piroxicam (PXM), a nonsteroidal anti-inflammatory drug, is an enolic benzothiazine and a potent member of the oxicam series. The drug suppresses the synthesis of proinflammatory enzymes, such as cyclo-oxygenases-1 and -2 (COX-1 and 2), downregulates the production of prostaglandins (PGs) and tromboxanes, and inhibits polyamines production by blocking ornithine decarboxylase induction involved in nonmelanoma skin carcinogenesis. In addition, PXM is able to induce tumor cell apoptosis and suppresses metalloproteinase 2 activities. Skin carcinogenesis is a multistep process in which the accumulation of genetic events leads to a gradually dysplastic cellular expression, deregulation of cell growth, and carcinomatous progression. COX-1 upregulation plays a significant role in PG and vascular epidermal growth factor production supporting tumor growth. Increased level of PGs in premalignant and/or malignant cutaneous tumors is also favored by upregulation of COX-2 and downregulation of the tumor suppressor gene 15-hydroxy-prostaglandin dehydrogenase. Chemoprevention can be a hopeful approach to inhibit carcinoma occurrence before an invasive tumor develops. The chemopreventive effect of nonsteroidal anti-inflammatory drugs on nonmelanoma skin cancers has been established. In this study, we highlighted the different modalities of action of PXM on the pathogenesis of nonmelanoma skin cancer, analyzing and evaluating binding modes and energies between COX-1 or COX-2 and PXM by protein-ligand molecular docking. Our clinical experience about the local use of PXM on actinic keratoses and field cancerization is also reported, confirming its efficacy as target therapy.

Indexed as

AnimalsAnticarcinogenic AgentsAnti-Inflammatory Agents, Non-SteroidalApoptosisCyclooxygenase InhibitorsHumansMatrix Metalloproteinase 2Molecular Docking SimulationPiroxicamSkin NeoplasmsAnticarcinogenic AgentsAnti-Inflammatory Agents, Non-SteroidalCyclooxygenase InhibitorsMatrix Metalloproteinase 2Piroxicamactinic keratosisbinding modeCOXs inhibitortumor progression

Identifiers

PMID26604686
PMCPMC4630202
OpenAlexW1850345829

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.