Evidence map›Paper›PMID 29689707›Full record

ArticleCancer biomarkers : section A of Disease markers2018

MDR1 not CYP3A4 gene expression is the predominant mechanism of innate drug resistance in pediatric soft tissue sarcoma patients.

Dora Molina-Ortiz, Carmen Torres-Zárate, Rocío Cárdenas-Cardós, José Martin Palacios-Acosta, Daniel Hernández-Arrazola, Jaime Shalkow-Klincovstein, Erick Díaz-Díaz, Araceli Vences-Mejía

Abstract read
In one paragraph

Article in Cancer biomarkers : section A of Disease markers, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. The free amino acid profiles and metabolic biomarkers of predicting the chemotherapeutic response in advanced sarcoma patients.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2020
    Article
  3. 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

8 authors at 1 institution in 1 country.

Dora Molina-OrtizLaboratory of Genetic Toxicology, National Institute of Pediatrics, Mexico City, Mexico.
Carmen Torres-ZárateLaboratory of Genetic Toxicology, National Institute of Pediatrics, Mexico City, Mexico.
Rocío Cárdenas-CardósDepartment of Pediatric Oncology, National Institute of Pediatrics, Mexico City, Mexico.
José Martin Palacios-AcostaOncological Surgery Service, National Institute of Pediatrics, Mexico City, Mexico.
Daniel Hernández-ArrazolaOncological Surgery Service, National Institute of Pediatrics, Mexico City, Mexico.
Jaime Shalkow-KlincovsteinOncological Surgery Service, National Institute of Pediatrics, Mexico City, Mexico.
Erick Díaz-DíazLaboratory of Genetic Toxicology, National Institute of Pediatrics, Mexico City, Mexico.
Araceli Vences-MejíaLaboratory of Genetic Toxicology, National Institute of Pediatrics, Mexico City, Mexico.
National Institute of Genomic Medicine · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIntratumoral up-regulation of genes coding for drug transporters and metabolizing enzymes, such as MDR1 and CYP3A4, after chemotherapy are linked to cancer drug resistance. However their expression in primary soft tissue sarcomas (STS) prior to drug treatment and their role in innate resistance remain unclear.

objectiveThe aim of this study was characterize MDR1 and CYP3A4 expression pattern before to chemotherapy and its clinical implication in pediatric STS.

methodsIn this prospective study we analyzed MDR1 and CYP3A4 mRNA expression in both normal and tumor tissues from 28 newly diagnosed STS pediatric and then compared with patients' clinical-pathological data, including chemotherapy response.

resultsOur data showed that the expression of the MDR1 gene was significantly higher in malignant tissue than in the normal tissues of patients with STS. In addition, high MDR1 expression was significantly associated with local advances, as well as poor response to treatment. In contrast, CYP3A4 expression level was negligible in both tumoral and non-tumoral tissues.

conclusionsThese results suggest that a significant mRNA level of MDR1 gene was intrinsically present in STS before exposure to chemotherapeutic drugs, suggesting that MDR1 may be important contributors of innate chemoresistance of this tumor type.

Indexed as

Gene Expression Regulation, NeoplasticAdolescentAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsATP Binding Cassette Transporter, Subfamily BCell Line, TumorChildChild, PreschoolCombined Modality TherapyCytochrome P-450 CYP3ADrug Resistance, NeoplasmFemaleHumansKaplan-Meier EstimateMaleNeoplasm StagingABCB1 protein, humanAntineoplastic AgentsATP Binding Cassette Transporter, Subfamily BCYP3A4 protein, humanCytochrome P-450 CYP3ARNA, MessengerchemoresistanceCYP3A4MDR1mRNA expression levelSoft tissue sarcomas

Identifiers

PMID29689707
PMCPMC13078427
OpenAlexW2802484062

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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.