Evidence map›Paper›PMID 33281885›Full record

ArticleFrontiers in genetics2020

Machine Learning Based Network Analysis Determined Clinically Relevant miRNAs in Breast Cancer.

Min Qiu, Qin Fu, Chunjie Jiang, Da Liu

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Precision Medicine Approaches with Metabolomics and Artificial Intelligence.International journal of molecular sciences · 2022
    Review
  5. Editorial: DNA Methylation Dynamics and Human Diseases.Frontiers in cell and developmental biology · 2022
    Article
  6. Article
  7. Article
  8. Article
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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

4 authors at 2 institutions in 2 countries.

Min QiuDepartment of Orthopedics, Shengjing Hospital of China Medical University, Shenyang, China.
Qin FuDepartment of Orthopedics, Shengjing Hospital of China Medical University, Shenyang, China.
Chunjie JiangInstitute for Diabetes, Obesity, and Metabolism, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Da LiuDepartment of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China.
China Medical University · CNUniversity of Pennsylvania · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsMicroRNAs (miRNAs) have been shown to play important roles in many cancers, including breast cancer. The majority of previous studies employed network analysis to identify key miRNAs in cancer progression. However, most of dysregulated miRNA networks were constructed based on the expression variation of miRNAs and target genes.

methodsThe relations between miRNAs and target genes were computed by Spearman correlation separately in breast cancer and normal breast samples. We calculated dysregulated scores based on the dysregulation of miRNA-mRNA regulatory relations. A dysregulated miRNA target network (DMTN) was constructed from the miRNA-mRNA pairs with significant dysregulated scores. SVM classifier was employed to predict breast cancer risk miRNAs from the DMTN. Hypermetric test was utilized to calculate the significance of overlap between different gene sets. Pearson correlation was used to evaluate associations between miRNAs/genes and drug response.

resultsThe DMTN comprised 511 miRNAs and was similar to common biological networks. Based on miRNAs and target genes in DMTN, we predicted 90 breast cancer risk miRNAs by using SVM classifier. Predicted risk miRNAs and one-step neighbor genes were significantly overlapping with differential miRNAs, cancer-related and housekeeping genes in breast cancer. These risk miRNAs were involved in many cancer-related and immune-related processes. In addition, most risk miRNAs were able to predict survival of breast cancer patients. More interestingly, some risk miRNAs and one-step neighbor genes were remarkably associated with immune cell infiltration. For example, high expression of hsa-miR-155 indicates high abundance of activated CD4+ T cells but low level of M2 macrophage infiltration. Furthermore, we identified 588 miRNA-drug and 3,146 gene-drug pairs, wherein the expression level of miRNAs/genes could indicate the sensitivity of cancer cells to anti-cancer drugs.

conclusionWe predicted 90 breast cancer risk miRNAs based on proposed DMTN by using SVM classifier. Predicted risk miRNAs are biologically and clinically relevant in breast cancer. Risk miRNAs and one-step neighbor genes could serve as biomarkers for immune cell infiltration and anti-cancer drug response, which sheds lights on immunotherapy or targeted therapy for patients with breast cancer.

Indexed as

breast cancerdrug responseimmune infiltrationmiRNASVM classifier

Identifiers

PMID33281885
PMCPMC7689188
OpenAlexW3106018642

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.