Evidence map›Paper›PMID 37138857›Full record

ReviewFrontiers in oral health2023

Heterogeneity and versatility of the extracellular matrix during the transition from pleomorphic adenoma to carcinoma ex pleomorphic adenoma: cumulative findings from basic research and new insights.

João Figueira Scarini, Reydson Alcides de Lima-Souza, Luccas Lavareze, Maria Clara Falcão Ribeiro de Assis, Ingrid Iara Damas, Albina Altemani, Erika Said Abu Egal, Jean Nunes Dos Santos, Ibrahim Olajide Bello, Fernanda Viviane Mariano

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in oral health, 2023. 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
3.8field-weighted citation impact, top 6% 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, 12 citations in OpenAlex.

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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

10 authors at 4 institutions in 3 countries.

João Figueira ScariniDepartment of Pathology, Faculty of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.
Reydson Alcides de Lima-SouzaDepartment of Pathology, Faculty of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.
Luccas LavarezeDepartment of Pathology, Faculty of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.
Maria Clara Falcão Ribeiro de AssisDepartment of Pathology, Faculty of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.
Ingrid Iara DamasDepartment of Pathology, Faculty of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.
Albina AltemaniDepartment of Pathology, Faculty of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.
Erika Said Abu EgalDepartment of Pathology, Faculty of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.
Jean Nunes Dos SantosDepartment of Oral and Maxillofacial Pathology, School of Dentistry, Federal University of Bahia, Salvador, Brazil.
Ibrahim Olajide BelloDepartment of Oral Medicine and Diagnostic Sciences, College of Dentistry, King Saud University, Riyadh, Saudi Arabia.
Fernanda Viviane MarianoDepartment of Pathology, Faculty of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.
Universidade Estadual de Campinas (UNICAMP) · BRHuntsman Cancer Institute · USKing Saud University · SAUniversidade Federal da Bahia · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pleomorphic adenoma (PA) is the most common salivary gland tumor, accounting for 50%-60% of these neoplasms. If untreated, 6.2% of PA may undergo malignant transformation to carcinoma ex-pleomorphic adenoma (CXPA). CXPA is a rare and aggressive malignant tumor, whose prevalence represents approximately 3%-6% of all salivary gland tumors. Although the pathogenesis of the PA-CXPA transition remains unclear, CXPA development requires the participation of cellular components and the tumor microenvironment for its progression. The extracellular matrix (ECM) comprises a heterogeneous and versatile network of macromolecules synthesized and secreted by embryonic cells. In the PA-CXPA sequence, ECM is formed by a variety of components including collagen, elastin, fibronectin, laminins, glycosaminoglycans, proteoglycans, and other glycoproteins, mainly secreted by epithelial cells, myoepithelial cells, cancer-associated fibroblasts, immune cells, and endothelial cells. Like in other tumors including breast cancer, ECM changes play an important role in the PA-CXPA sequence. This review summarizes what is currently known about the role of ECM during CXPA development.

Indexed as

carcinogenesiscarcinoma ex pleomorphic adenoma (CXPA)extracellular matrix (ECM)pleomorphic adenoma (PA)review

Identifiers

PMID37138857
PMCPMC10149834
OpenAlexW4366221538

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.