Evidence map›Paper›PMID 25496125›Full record

ArticleBMC medical genomics2014

Overexpression of miR-21-5p as a predictive marker for complete tumor regression to neoadjuvant chemoradiotherapy in rectal cancer patients.

Camila Miranda Lopes-Ramos, Angelita Habr-Gama, Bruna de Souza Quevedo, Natália Mariana Felício, Fabiana Bettoni, Fernanda Christtanini Koyama, Paula Fontes Asprino, Pedro Alexandre Galante, Joaquim Gama-Rodrigues, Anamaria Aranha Camargo and 2 more

Open access · goldAbstract read
In one paragraph

Article in BMC medical genomics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 2 pooled it
2.7field-weighted citation impact, top 9% 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

41 citing papers in PubMed, 2 syntheses or guidelines pooled it, 70 citations in OpenAlex.

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  10. The Roles of Non-Coding RNAs in Radiotherapy of Gastrointestinal Carcinoma.Frontiers in cell and developmental biology · 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

12 authors at 6 institutions in 2 countries.

Camila Miranda Lopes-RamosCentro de Oncologia Molecular, Hospital Sírio-Libanês, São Paulo, Brazil. cramos@mochsl.org.br.
Angelita Habr-GamaAngelita & Joaquim Gama Institute, São Paulo, Brazil. gamange@uol.com.br.
Bruna de Souza QuevedoLudwig Institute for Cancer Research, São Paulo, Brazil. gluts2005@gmail.com.
Natália Mariana FelícioAngelita & Joaquim Gama Institute, São Paulo, Brazil. nmfelicio@gmail.com.
Fabiana BettoniCentro de Oncologia Molecular, Hospital Sírio-Libanês, São Paulo, Brazil. fbettoni@mochsl.org.br.
Fernanda Christtanini KoyamaCentro de Oncologia Molecular, Hospital Sírio-Libanês, São Paulo, Brazil. fkoyama@mochsl.org.br.
Paula Fontes AsprinoCentro de Oncologia Molecular, Hospital Sírio-Libanês, São Paulo, Brazil. pasprino@mochsl.org.br.
Pedro Alexandre GalanteCentro de Oncologia Molecular, Hospital Sírio-Libanês, São Paulo, Brazil. pgalante@mochsl.org.br.
Joaquim Gama-RodriguesAngelita & Joaquim Gama Institute, São Paulo, Brazil. gama@ajgama.com.br.
Anamaria Aranha CamargoCentro de Oncologia Molecular, Hospital Sírio-Libanês, São Paulo, Brazil. aacamargo@mochsl.org.br.
Rodrigo Oliva PerezAngelita & Joaquim Gama Institute, São Paulo, Brazil. rodrigo.operez@gmail.com.
Raphael Bessa ParmigianiCentro de Oncologia Molecular, Hospital Sírio-Libanês, São Paulo, Brazil. raphaparmigiani@gmail.com.br.
Hospital Sírio-Libanês · BRLudwig Cancer Research · BEUniversidade de São Paulo · BRFundação de Estudos e Pesquisas Aquáticas · BRHospital Alemão Oswaldo Cruz · BRUniversity Gama Filho · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeoadjuvant chemoradiotherapy (nCRT) followed by radical surgery is the preferred treatment strategy for locally advanced rectal cancer. However, complete tumor regression is observed in a significant proportion of patients after nCRT, making them ideal candidates for alternative treatment strategies to this considerably morbid procedure. Identification of such patients based on clinical findings (complete clinical response - cCR) is difficult mainly because it relies on subjective clinical and imaging studies. Our goal was to identify biomarkers capable of predicting complete response to nCRT.

methodsWe analyzed miRNA expression profile using deep sequencing in rectal tumor biopsies prior to nCRT. Differential expression was investigated by EdgeR for a training (n = 27) and a validation (n = 16) set of patients to identify miRNAs associated with treatment response (complete vs. incomplete). In vitro experiments with two cancer cell lines were also performed in order to evaluate the possible role of miRNAs on response to nCRT.

resultsWe found 4 miRNAs differentially expressed between complete and incomplete responders to nCRT. In addition, validation was performed using an independent group of patients and miR-21-5p was confirmed as being overexpressed in complete responders. Overall sensitivity and specificity of miR-21-5p expression in predicting complete response to nCRT was 78% and 86% respectively. Interestingly, in a subset of patients with cCR followed by early local recurrence, the expression level of miR-21-5p was considerably low, similarly to incomplete responders. We also found SATB1, a miR-21-5p target gene and known multidrug resistance gene, whose expression was inversely correlated with miR-21-5p expression. Finally, we performed functional experiments and showed that miR-21-5p and SATB1 may be directly involved with poor response to nCRT in rectal cancer patients.

conclusionsThis study suggests miR-21-5p as a promising predictive biomarker, which should aid in the selection of patients with cCR to nCRT that potentially could be spared from radical surgery.

Indexed as

ChemoradiotherapyNeoadjuvant TherapyAdenocarcinomaAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorFemaleFollow-Up StudiesGene Expression Regulation, NeoplasticHigh-Throughput Nucleotide SequencingHumansMaleMatrix Attachment Region Binding ProteinsMicroRNAsMiddle AgedNeoplasm Recurrence, LocalNeoplasm StagingBiomarkers, TumorMatrix Attachment Region Binding ProteinsMicroRNAsMIRN21 microRNA, humanSATB1 protein, human

Identifiers

PMID25496125
PMCPMC4279677
OpenAlexW2123899702

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.