Evidence map›Paper›PMID 29843219›Full record

ArticleCancer biomarkers : section A of Disease markers2018

The clinicopathological and prognostic significances of Dkk3 expression in cancers: A bioinformatics analysis.

Guan-Yu Chen, Hua-Chuan Zheng

Abstract read
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Article in Cancer biomarkers : section A of Disease markers, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 40% of its field
1 · What the graph read from it

What it found

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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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Wnt antagonist as therapeutic targets in ovarian cancer.The international journal of biochemistry & cell biology · 2022
    Review
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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

2 authors.

Guan-Yu Chen
Hua-Chuan Zheng

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDkk3 protein attenuates the expression of Wnt3a, Wnt5a and LRP6, and their interaction, and interacts with βTrCP to suppress wnt/β-catenin pathway.

methodsWe performed a bioinformatics analysis of Dkk3 mRNA expression through Oncomine, TCGA and Kaplan-Meier plotter databases up to July 10, 2017.

resultsUp-regulated Dkk3 expression was higher in gastric, breast, and ovarian cancers than normal tissues (p< 0.05). Bitter's database showed a higher Dkk3 expression in ovarian cytoadenocarcinoma than clear cell adenocarcinoma (p< 0.05). Dkk3 was more expressed in ductal breast cancer in situ than invasive ductal breast cancer (p< 0.05), in mixed lobular and ductal cancer, and lobular cancer than ductal breast cancer (p< 0.05). In TCGA data, Dkk3 expression was lower in gastric cancers with than without Barret's esophagus (p< 0.05), in intestinal-type than diffuse-type cancers (p< 0.05), and in the cancers of elder than younger patients (p< 0.05). Dkk3 expression was higher in squamous cell carcinoma than adenocarcinoma (p< 0.05). Dkk3 expression was higher in ductal than lobular breast cancer, or in younger than elder patients with breast cancer (p< 0.05). According to Kaplan-Meier plotter, Dkk3 expression was negatively correlated with overall, progression-free, relapse-free or distant-metastasis-free survival rate of gastric, breast or ovarian cancer patients, but versa for lung cancer patients (p< 0.05).

conclusionDkk3 expression might be employed as a potential marker to indicate carcinogenesis and histogenesis, even prognosis.

Indexed as

Computational BiologyAdaptor Proteins, Signal TransducingBiomarkers, TumorCarcinogenesisChemokinesGene Expression Regulation, NeoplasticHumansIntercellular Signaling Peptides and ProteinsKaplan-Meier EstimateNeoplasmsProgression-Free SurvivalAdaptor Proteins, Signal TransducingBiomarkers, TumorChemokinesDKK3 protein, humanIntercellular Signaling Peptides and Proteinsaggressivenessbioinformatics analysiscarcinogenesisDkk3prognosis

Identifiers

PMID29843219
PMCPMC13078561
OpenAlexW2804451598

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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.