Evidence map›Paper›PMID 35163066›Full record

ArticleInternational journal of molecular sciences2022

Paclitaxel-Induced Epidermal Alterations: An In Vitro Preclinical Assessment in Primary Keratinocytes and in a 3D Epidermis Model.

Paula Montero, Javier Milara, Martín Pérez-Leal, Cristina Estornut, Inés Roger, Alejandro Pérez-Fidalgo, Celia Sanz, Julio Cortijo

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

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  9. Molecular Research and Treatment of Skin Diseases.International journal of molecular sciences · 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

8 authors at 4 institutions in 1 country.

Paula MonteroDepartment of Pharmacology, Faculty of Medicine, University of Valencia, 46010 Valencia, Spain.
Javier MilaraDepartment of Pharmacology, Faculty of Medicine, University of Valencia, 46010 Valencia, Spain.
Martín Pérez-LealFaculty of Health Sciences, Universidad Europea de Valencia, 46010 Valencia, Spain.ORCID 0000-0002-1313-3449
Cristina EstornutDepartment of Pharmacology, Faculty of Medicine, University of Valencia, 46010 Valencia, Spain.
Inés RogerDepartment of Pharmacology, Faculty of Medicine, University of Valencia, 46010 Valencia, Spain.
Alejandro Pérez-FidalgoDepartment of Medical Oncology, University Clinic Hospital of Valencia, 46010 Valencia, Spain.ORCID 0000-0003-3568-4345
Celia SanzDepartment of Pharmacology, Faculty of Medicine, University of Valencia, 46010 Valencia, Spain.
Julio CortijoDepartment of Pharmacology, Faculty of Medicine, University of Valencia, 46010 Valencia, Spain.
Universitat de València · ESHospital Clínico Universitario de Valencia · ESUniversidad Europea de Madrid · ESUniversitat Jaume I · ES

Funding

Centro de investigación biomédica en enfermedades respiratorias (CIBERES) CB06/06/0027Fondo Europeo de Desarrollo Regional (FEDER) PID2020-114871RB-I00Instituto de Salud Carlos III PI20/01363Regional Government Generalitat Valenciana Prometeo 2017/023/UV
6 · The paper itself

Abstract

Paclitaxel is a microtubule-stabilizing chemotherapeutic agent approved for the treatment of ovarian, non-small cell lung, head, neck, and breast cancers. Despite its beneficial effects on cancer and widespread use, paclitaxel also damages healthy tissues, including the skin. However, the mechanisms that drive these skin adverse events are not clearly understood. In the present study, we demonstrated, by using both primary epidermal keratinocytes (NHEK) and a 3D epidermis model, that paclitaxel impairs different cellular processes: paclitaxel increased the release of IL-1α, IL-6, and IL-8 inflammatory cytokines, produced reactive oxygen species (ROS) release and apoptosis, and reduced the endothelial tube formation in the dermal microvascular endothelial cells (HDMEC). Some of the mechanisms driving these adverse skin events in vitro are mediated by the activation of toll-like receptor 4 (TLR-4), which phosphorylate transcription of nuclear factor kappa B (NF-κb). This is the first study analyzing paclitaxel effects on healthy human epidermal cells with an epidermis 3D model, and will help in understanding paclitaxel's effects on the skin.

Indexed as

AnimalsBALB 3T3 CellsCells, CulturedCell SurvivalCytokinesDermisEndothelial CellsEpidermisGene Expression RegulationHumansInterleukin-1alphaInterleukin-6Interleukin-8KeratinocytesMiceNF-kappa BCXCL8 protein, humanCytokinesIL1A protein, humanIL6 protein, humanInterleukin-1alphaInterleukin-6Interleukin-8NF-kappa BPaclitaxelReactive Oxygen SpeciesTLR4 protein, humanToll-Like Receptor 43D epidermis modelepidermisNHEKpaclitaxel

Identifiers

PMID35163066
PMCPMC8834980
OpenAlexW4206624811

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.