Evidence map›Paper›PMID 37561760›Full record

ArticlePloS one2023

Identification of monotonically expressed long non-coding RNA signatures for breast cancer using variational autoencoders.

Dongjiao Wang, Ling Gao, Xinliang Gao, Chi Wang, Suyan Tian

Abstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Dongjiao WangDepartment of Gynecological Oncology, The First Hospital of Jilin University, Changchun, Jilin, People's Republic of China.
Ling GaoDepartment of Radiation Oncology, The First Hospital of Jilin University, Changchun, Jilin, People's Republic of China.
Xinliang GaoDepartment of Thoracic Surgery, The First Hospital of Jilin University, Changchun, Jilin, People's Republic of China.
Chi WangDepartment of Internal Medicine, College of Medicine, University of Kentucky, Lexington, Kentucky, United States of America.
Suyan TianDivision of Clinical Research, The First Hospital of Jilin University, Changchun, Jilin, People's Republic of China.ORCID 0000-0002-5942-1542

Funding

University of Kentucky Markey Cancer Center Support Grant ECIA SupplementP30CA177558 · NCI · UNIVERSITY OF KENTUCKY · PI Jennifer F Rogers · 2013 to 2026
$38.3M
NCI NIH HHS P30 CA177558
6 · The paper itself

Abstract

As breast cancer is a multistage progression disease resulting from a genetic sequence of mutations, understanding the genes whose expression values increase or decrease monotonically across pathologic stages can provide insightful clues about how breast cancer initiates and advances. Utilizing variational autoencoder (VAE) networks in conjunction with traditional statistical testing, we successfully ascertain long non-coding RNAs (lncRNAs) that exhibit monotonically differential expression values in breast cancer. Subsequently, we validate that the identified lncRNAs really present monotonically changed patterns. The proposed procedure identified 248 monotonically decreasing expressed and 115 increasing expressed lncRNAs. They correspond to a total of 65 and 33 genes respectively, which possess unique known gene symbols. Some of them are associated with breast cancer, as suggested by previous studies. Furthermore, enriched pathways by the target mRNAs of these identified lncRNAs include the Wnt signaling pathway, human papillomavirus (HPV) infection, and Rap 1 signaling pathway, which have been shown to play crucial roles in the initiation and development of breast cancer. Additionally, we trained a VAE model using the entire dataset. To assess the effectiveness of the identified lncRNAs, a microarray dataset was employed as the test set. The results obtained from this evaluation were deemed satisfactory. In conclusion, further experimental validation of these lncRNAs with a large-sized study is warranted, and the proposed procedure is highly recommended.

Indexed as

Breast NeoplasmsRNA, Long NoncodingFemaleGene Expression ProfilingHumansOligonucleotide Array Sequence AnalysisRNA, MessengerWnt Signaling PathwayRNA, Long NoncodingRNA, Messenger

Identifiers

PMID37561760
PMCPMC10414641

What Socratic holds

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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 Socratic graph.