Evidence map›Paper›PMID 40136335›Full record

ArticleCurrent oncology (Toronto, Ont.)2025

Aberrant Expression of CYP2W1 in Pediatric Soft Tissue Sarcomas: Clinical Significance and Potential as a Therapeutic Target.

Dora Molina-Ortiz, Carmen Torres-Zárate, Rocío Cárdenas-Cardós, Daniel Hernández-Arrazola, Marco R Aguilar-Ortiz, José Palacios-Acosta, Jaime Shalkow-Klincovstein, Víctor Dorado-González, Rebeca Santes-Palacios, Elizabeth Hernández-Urzúa and 1 more

Abstract read
In one paragraph

Article in Current oncology (Toronto, Ont.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. 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

11 authors.

Dora Molina-OrtizLaboratory of Genetic Toxicology, National Institute of Pediatrics, Mexico City 04530, Mexico.
Carmen Torres-ZárateLaboratory of Genetic Toxicology, National Institute of Pediatrics, Mexico City 04530, Mexico.
Rocío Cárdenas-CardósDepartment of Pediatric Oncology, National Institute of Pediatrics, Mexico City 04530, Mexico.
Daniel Hernández-ArrazolaDepartment of Oncological Surgery, National Institute of Pediatrics, Mexico City 04530, Mexico.
Marco R Aguilar-OrtizDepartment of Pediatric Oncology, National Institute of Pediatrics, Mexico City 04530, Mexico.
José Palacios-AcostaDepartment of Oncological Surgery, National Institute of Pediatrics, Mexico City 04530, Mexico.
Jaime Shalkow-KlincovsteinDepartment of Oncological Surgery, National Institute of Pediatrics, Mexico City 04530, Mexico.ORCID 0000-0003-0056-3455
Víctor Dorado-GonzálezLaboratory of Genetic Toxicology, National Institute of Pediatrics, Mexico City 04530, Mexico.
Rebeca Santes-PalaciosLaboratory of Genetic Toxicology, National Institute of Pediatrics, Mexico City 04530, Mexico.ORCID 0000-0001-7310-5178
Elizabeth Hernández-UrzúaLaboratory of Genetic Toxicology, National Institute of Pediatrics, Mexico City 04530, Mexico.
Araceli Vences-MejíaLaboratory of Genetic Toxicology, National Institute of Pediatrics, Mexico City 04530, Mexico.

Funding

Consejo Nacional de Humanidades, Ciencias y Tecnologías 86395 and 262423
6 · The paper itself

Abstract

Pediatric soft-tissue sarcomas (STSs) are aggressive malignancies with poor prognoses, particularly in recurrent and metastatic cases. Standard therapies, such as cytotoxic chemotherapy, offer limited survival benefits and carry significant toxicities, underscoring the urgent need for innovative therapeutic approaches. CYP2W1, a tumor-specific monooxygenase enzyme, has emerged as a promising therapeutic target due to its aberrant expression in various cancers. However, its role in pediatric STSs remains poorly understood. This study evaluated CYP2W1 expression in 42 pediatric STS samples across seven histological subtypes using qPCR and Western blot analyses. High CYP2W1 expression was detected in 69% of tumor samples at the mRNA level and in 40.5% at the protein level, compared to absent or negligible expression in matched normal tissues (

Indexed as

Cytochrome P450 Family 2SarcomaAdolescentChildChild, PreschoolClinical RelevanceFemaleHumansMaleCYP2W1 protein, humanCytochrome P450 Family 2aberrant expressioncytochrome P450 2W1 (CYP2W1)immunotherapypediatric patientsprodrug activationrhabdomyosarcomasoft-tissue sarcomas (STSs)STS subtypessynovial sarcomatherapeutic target

Identifiers

PMID40136335
PMCPMC11941694

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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.