Evidence map›Paper›PMID 35036444›Full record

ArticleBioMed research international2022

DOK5 as a Prognostic Biomarker of Gastric Cancer Immunoinvasion: A Bioinformatics Analysis.

Fengyong Luo, Zhihuai Wang, Shuai Chen, Zhenbo Luo, Gaochao Wang, Haojun Yang, Liming Tang

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2022. 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
0.6field-weighted citation impact, top 33% 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, 4 citations in OpenAlex.

  1. Review
  2. Article
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

7 authors at 2 institutions in 1 country.

Fengyong Luo *School of Graduate, Dalian Medical University, Dalian, Liaoning 116044, China.ORCID https://orcid.org/0000-0001-6089-5975
Zhihuai Wang *School of Graduate, Dalian Medical University, Dalian, Liaoning 116044, China.ORCID https://orcid.org/0000-0001-7156-3132
Shuai ChenCenter of Gastrointestinal Disease, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, Jiangsu 213000, China.ORCID https://orcid.org/0000-0003-2499-3281
Zhenbo LuoSchool of Graduate, Dalian Medical University, Dalian, Liaoning 116044, China.ORCID https://orcid.org/0000-0001-8968-7088
Gaochao WangSchool of Graduate, Dalian Medical University, Dalian, Liaoning 116044, China.ORCID https://orcid.org/0000-0001-9203-060X
Haojun YangCenter of Gastrointestinal Disease, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, Jiangsu 213000, China.ORCID https://orcid.org/0000-0003-1421-554X
Liming TangCenter of Gastrointestinal Disease, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, Jiangsu 213000, China.ORCID https://orcid.org/0000-0002-3730-3131
Dalian Medical University · CNChangzhou No.2 People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDocking protein 5 (DOK5) is a member of the docking protein group of membrane proteins and is an adapter protein involved in signal transduction. Nevertheless, the role of DOK5 expression in the prognosis of gastric cancer (GC) remains unclear.

methodsIn this study, clinical prognostic parameters and survival data related to DOK5, in patients with GC, were analyzed using bioinformatics analysis comprising Oncomine and TIMER, UALCAN database, Kaplan-Meier plotter, GEPIA, GSEA, DAVID, and cBioPortal websites.

resultsIn our study, GC contained various DOK5 expressions, which forecasted poor survival outcomes. Moreover, our research showed that high DOK5 could predict high-level infiltration of several GC immune cells, as evidenced by M1, TAM, M2, B cell, and T cell failure. Hence, DOK5 might become a new gastric cancer biomarker and therapeutic target. In the following analysis, in order to explore the prognostic value of DOK5 in GC, more clinical trials are needed to validate our results.

conclusionsThrough multiple database verifications, DOK5 was found to be part of the pathogenic genes for GC. Thus, it can change the formation and progression of tumors by acting on human immunity.

Indexed as

Databases, Nucleic AcidStomach NeoplasmsAdaptor Proteins, Signal TransducingBiomarkers, TumorDisease-Free SurvivalFemaleHumansKaplan-Meier EstimateMaleNeoplasm InvasivenessNeoplasm ProteinsSurvival RateAdaptor Proteins, Signal TransducingBiomarkers, TumorDOK5 protein, humanNeoplasm Proteins

Identifiers

PMID35036444
PMCPMC8754673
OpenAlexW4206731669

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.