Evidence map›Paper›PMID 34184566›Full record

ArticleTechnology in cancer research & treatment

Investigation of Candidate Genes and Pathways in Basal/TNBC Patients by Integrated Analysis.

Qi Liu, Xiang Song, Zhaoyun Liu, Zhiyong Yu

Open access · goldAbstract read
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Article in Technology in cancer research & treatment. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 29% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

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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 1 country.

Qi LiuSchool of Medicine, Shandong University, Jinan, People's Republic of China.ORCID 0000-0003-4217-0641
Xiang SongDepartment of Breast Surgery, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong, People's Republic of China.
Zhaoyun LiuSchool of Medicine, Shandong University, Jinan, People's Republic of China.
Zhiyong YuDepartment of Breast Surgery, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong, People's Republic of China.
Shandong Tumor Hospital · CNShandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis study aims to identify the key pathway and related genes and to further explore the potential molecular mechanisms of triple negative breast cancer (TNBC).

methodsThe transcriptome data and clinical information of breast cancer patients were downloaded from the TCGA database, including 94 cases of paracancerous tissue, 225 cases of Basal like type, 151 cases of Her2 type, 318 cases of Luminal type A, 281 cases of Luminal type B, and 89 cases of Normal Like type. The differentially expressed genes (DEGs) were identified based on the criteria of |logFC|≥1.5 and adjust

resultsA total of 533 DEGs were identified. Functional annotation showed that DEGs were significantly enriched in intermediate filament cytoskeleton, DNA-binding transcription activator activity, epidermis development, and Neuroactive ligand-receptor interaction. Survival analysis found that FOXD1, DLL3, and LY6D showed significant correlation with the prognosis of patients with the Basal-like type (

conclusionThe DEGs and their enriched functions and pathways identified in this study contribute to the understanding of the molecular mechanisms of TNBC. In addition, FOXD1, DLL3, and LY6D may be defined as the prognostic markers and potential therapeutic targets for TNBC patients.

Indexed as

Cell SurvivalAntibiotics, AntineoplasticCell Adhesion MoleculesCell Line, TumorDatabases, GeneticDoxorubicinFemaleForkhead Transcription FactorsGene Knockdown TechniquesGene OntologyGPI-Linked ProteinsHumansIntracellular Signaling Peptides and ProteinsKaplan-Meier EstimateMembrane ProteinsMetabolic Networks and PathwaysAntibiotics, AntineoplasticCell Adhesion MoleculesDLL3 protein, humanDoxorubicinForkhead Transcription FactorsFOXD1 protein, humanGPI-Linked ProteinsIntracellular Signaling Peptides and ProteinsLY6D protein, humanMembrane Proteinsidentification of key genessurvival prognosisThe Cancer Genome Atlastriple negative breast cancer

Identifiers

PMID34184566
PMCPMC8246569
OpenAlexW3177228147

What OpenQuestion holds

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LicenceCC BY-NC
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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.