Evidence mapPaperPMID 42545402Full record

ArticleMolecular biology reports2026

Upregulation of paraoxonase-2 enzyme in human osteosarcoma and its involvement in mechanisms promoting the aggressive behavior of tumor cells.

Eleonora Gerini, Veronica Pompei, Monia Cecati, Roberto Campagna, Valentina Pozzi, Alessandra Filosa, Gaia Goteri, Eleonora Salvolini, Monica Emanuelli, Davide Sartini

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Article in Molecular biology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Eleonora Gerini *Department of Clinical Sciences, Polytechnic University of Marche, Ancona, 60126, Italy.
Veronica Pompei *Department of Clinical Sciences, Polytechnic University of Marche, Ancona, 60126, Italy.ORCID http://orcid.org/0000-0002-3747-9348
Monia Cecati *Department for the Promotion of Human Science and Quality of Life, San Raffaele Roma University, Via di Val Cannuta, 247, Rome, 00166, Italy.ORCID http://orcid.org/0000-0003-4947-5157
Roberto CampagnaDepartment for the Promotion of Human Science and Quality of Life, San Raffaele Roma University, Via di Val Cannuta, 247, Rome, 00166, Italy. roberto.campagna@uniroma5.it.ORCID https://orcid.org/0000-0003-2607-2734
Valentina PozziDepartment of Clinical Sciences, Polytechnic University of Marche, Ancona, 60126, Italy. v.pozzi@univpm.it.ORCID http://orcid.org/0000-0003-3941-0341
Alessandra FilosaDepartment of Biomedical Sciences and Public Health, Polytechnic University of Marche, Via Tronto 10/a, Ancona, 60126, Italy.ORCID http://orcid.org/0000-0002-4071-4898
Gaia GoteriDepartment of Biomedical Sciences and Public Health, Polytechnic University of Marche, Via Tronto 10/a, Ancona, 60126, Italy.ORCID http://orcid.org/0000-0001-5198-8387
Eleonora SalvoliniDepartment of Clinical Sciences, Polytechnic University of Marche, Ancona, 60126, Italy.ORCID http://orcid.org/0000-0003-2405-8947
Monica EmanuelliDepartment of Clinical Sciences, Polytechnic University of Marche, Ancona, 60126, Italy.ORCID http://orcid.org/0000-0002-8520-519X
Davide SartiniDepartment of Clinical Sciences, Polytechnic University of Marche, Ancona, 60126, Italy.ORCID http://orcid.org/0000-0003-3879-8647

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOsteosarcoma (OS) is the most common bone cancer, known for its aggressive nature, high chemoresistance, and strong metastatic potential responsible for poor clinical outcomes. In this context, identifying reliable biomarkers and therapeutic targets is therefore critical. This study investigates the role of paraoxonase-2 (PON2), an intracellular enzyme known for its anti-oxidative and anti-apoptotic properties. PON2 overexpression has been observed in various cancers and is implicated in tumor development and progression. METHODS AND

resultsPON2 expression was evaluated by immunohistochemistry in bone tissue samples from OS patients and control subjects. shRNA-mediated PON2 silencing was performed in U-2 OS and Saos-2 cells to assess proliferation, viability, migration, chemosensitivity, ROS production, apoptosis activation, glucose uptake, and GLUT1 expression. PON2 overexpression and N-acetylcysteine (NAC) pre-treatment in CDDP-treated U-2 OS cells were used as rescue approaches. Preliminary analyses showed markedly higher PON2 expression in OS than in control bone specimens. PON2 knockdown reduced proliferation, viability, and migration, while enhancing sensitivity to cisplatin (U-2 OS and Saos-2) and doxorubicin (U-2 OS only); these effects were reversed by PON2 upregulation. PON2 silencing also increased ROS levels and caspase expression, and impaired glucose uptake by reducing GLUT1 expression and intracellular glucose levels. Since NAC did not fully rescue these alterations, PON2 appears to sustain chemoresistance by affecting important mechanisms related to ROS detoxification, glucose metabolism, and anti-apoptotic signaling.

conclusionsObtained data clearly illustrate the potential of PON2 as promising biomarker and molecular therapeutic target for human OS.

Indexed as

AryldialkylphosphataseBone NeoplasmsOsteosarcomaApoptosisCell Line, TumorCell MovementCell ProliferationCell SurvivalCisplatinDoxorubicinDrug Resistance, NeoplasmFemaleGene Expression Regulation, NeoplasticGlucose Transporter Type 1HumansMaleAryldialkylphosphataseCisplatinDoxorubicinGlucose Transporter Type 1PON2 protein, humanReactive Oxygen SpeciesChemoresistanceOsteosarcomaOxidative stressParaoxonase-2

Identifiers

PMID42545402

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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 Socratic graph.