Evidence map›Paper›PMID 34638391›Full record

ArticleCancers2021

Comparison of the Metastasis Predictive Potential of mRNA and Long Non-Coding RNA Profiling in Systemically Untreated Breast Cancer.

Thi T N Do, Ines Block, Mark Burton, Kristina P Sørensen, Martin J Larsen, Martin Bak, Søren Cold, Mads Thomassen, Qihua Tan, Torben A Kruse

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 89% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  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

10 authors at 2 institutions in 1 country.

Thi T N DoDepartment of Clinical Genetics, Odense University Hospital, 5000 Odense C, Denmark.
Ines BlockDepartment of Clinical Genetics, Odense University Hospital, 5000 Odense C, Denmark.
Mark BurtonDepartment of Clinical Genetics, Odense University Hospital, 5000 Odense C, Denmark.ORCID 0000-0002-3782-5933
Kristina P SørensenDepartment of Clinical Genetics, Odense University Hospital, 5000 Odense C, Denmark.
Martin J LarsenDepartment of Clinical Genetics, Odense University Hospital, 5000 Odense C, Denmark.ORCID 0000-0003-4107-8771
Martin BakDepartment of Pathology, Odense University Hospital, 5000 Odense C, Denmark.
Søren ColdDepartment of Oncology, Odense University Hospital, 5000 Odense C, Denmark.
Mads ThomassenDepartment of Clinical Genetics, Odense University Hospital, 5000 Odense C, Denmark.
Qihua TanHuman Genetics, Department of Clinical Research, University of Southern Denmark, 5000 Odense C, Denmark.
Torben A KruseDepartment of Clinical Genetics, Odense University Hospital, 5000 Odense C, Denmark.
University of Southern Denmark · DKOdense University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several gene expression signatures based on mRNAs and a few based on long non-coding RNAs (lncRNAs) have been developed to provide prognostic information beyond clinical evaluation in breast cancer (BC). However, the comparison of such signatures for predicting recurrence is very scarce. Therefore, we compared the prognostic utility of mRNAs and lncRNAs in low-risk BC patients using two different classification strategies. Frozen primary tumor samples from 160 lymph node negative and systemically untreated BC patients were included; 80 developed recurrence-i.e., regional or distant metastasis while 80 remained recurrence-free (mean follow-up of 20.9 years). Patients were pairwise matched for clinicopathological characteristics. Classification based on differential mRNA or lncRNA expression using seven individual machine learning methods and a voting scheme classified patients into risk-subgroups. Classification by the seven methods with a fixed sensitivity of ≥90% resulted in specificities ranging from 16-40% for mRNA and 38-58% for lncRNA, and after voting, specificities of 38% and 60% respectively. Classifier performance based on an alternative classification approach of balanced accuracy optimization also provided higher specificities for lncRNA than mRNA at comparable sensitivities. Thus, our results suggested that classification followed by voting improved prognostic power using lncRNAs compared to mRNAs regardless of classification strategy.

Indexed as

long non-coding RNAlow-risk breast cancerlymph node negativemachine learning methodsmRNAprognostic predictorssystemically untreated patients

Identifiers

PMID34638391
PMCPMC8508163
OpenAlexW3204521525

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.