Evidence map›Paper›PMID 32753649›Full record

ArticleOncogene2020

DOCK6 promotes chemo- and radioresistance of gastric cancer by modulating WNT/β-catenin signaling and cancer stem cell traits.

Hsiang-Cheng Chi, Chung-Ying Tsai, Chia-Siu Wang, Huang-Yu Yang, Chien-Hui Lo, Won-Jing Wang, Kam-Fai Lee, Li-Yin Lai, Ji-Hong Hong, Yen-Fang Chang and 7 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.6field-weighted citation impact, top 8% 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

31 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Review
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  4. Decoding Rho GTPase signalling networks in directed cell migration.Frontiers in cell and developmental biology · 2026
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  12. Wnt signaling and tumors (Review).Molecular and clinical oncology · 2024
    Review
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  15. Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. Diagnostics (Basel, Switzerland) · 2022
    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

17 authors at 8 institutions in 2 countries.

Hsiang-Cheng Chi *Radiation Biology Research Center, Institute for Radiological Research, Chang Gung University/Chang Gung Memorial Hospital, Linkou, Taoyuan, Taiwan.ORCID http://orcid.org/0000-0001-5691-2453
Chung-Ying Tsai *Kidney Research Center, Department of Nephrology, Chang Gung Memorial Hospital, Taoyuan, Taiwan.
Chia-Siu Wang *Department of General Surgery, Chang Gung Memorial Hospital, Chiayi, Taiwan.ORCID http://orcid.org/0000-0002-9357-2571
Huang-Yu Yang *Kidney Research Institute, Nephrology Department, Chang Gung Memorial Hospital, College of Medicine, Chang Gung University, Taoyuan, Taiwan.
Chien-Hui LoInstitute of Biochemistry and Molecular Biology, College of Life Science, National Yang-Ming University, Taipei, Taiwan.
Won-Jing WangInstitute of Biochemistry and Molecular Biology, College of Life Science, National Yang-Ming University, Taipei, Taiwan.
Kam-Fai LeeDepartment of Pathology, Chang Gung Memorial Hospital, Chiayi, Taiwan.
Li-Yin LaiDepartment of Microbiology and Internal Medicine, National Taiwan University, Taipei, Taiwan.ORCID http://orcid.org/0000-0003-0244-6834
Ji-Hong HongDepartment of Radiation Oncology, Institute for Radiological Research, Chang Gung Memorial Hospital at Linkou, Taoyuan, Taiwan.
Yen-Fang ChangGraduate Institute of Biomedical Sciences, College of Medicine, Chang-Gung University, Taoyuan, Taiwan.
Ming-Ming TsaiDepartment of General Surgery, Chang Gung Memorial Hospital, Chiayi, Taiwan.
Chau-Ting YehLiver Research Center, Chang Gung Memorial Hospital, Linkou, Taoyuan, Taiwan.
Cheng Heng WuDepartment of Biochemistry, College of Medicine, Chang-Gung University, Taoyuan, Taiwan.
Ching-Chuan HsiehDepartment of General Surgery, Chang Gung Memorial Hospital, Chiayi, Taiwan.
Lu-Hai Wang *Graduate Institute of Integrated Medicine, China Medical University, Taichung, Taiwan. lu-hai.wang@nhri.org.tw.
Wei-Jan Chen *Division of Cardiology, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan. wjchen@adm.cgmh.org.tw.ORCID http://orcid.org/0000-0001-8088-5475
Kwang-Huei Lin *Department of Biochemistry, College of Medicine, Chang-Gung University, Taoyuan, Taiwan. khlin@mail.cgu.edu.tw.ORCID http://orcid.org/0000-0002-5649-2222
Chang Gung University · TWChang Gung Memorial Hospital · TWChiayi Chang Gung Memorial Hospital · TWChang Gung University of Science and Technology · TWNational Yang Ming Chiao Tung University · TWJohns Hopkins University · USNational Health Research Institutes · TWNational Taiwan University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastric cancer (GC) is the third leading cause of cancer-related mortality worldwide and prognosis after potentially curative gastrectomy remains poor. Administration of GC-targeting molecules in combination with adjuvant chemo- or radiotherapy following surgical resection has been proposed as a potentially effective treatment option. Here, we have identified DOCK6, a guanine nucleotide exchange factor (GEF) for Rac1 and CDC42, as an independent biomarker for GC prognosis. Clinical findings indicate the positive correlation of higher DOCK6 expression with tumor size, depth of invasion, lymph node metastasis, vascular invasion, and pathological stage. Furthermore, elevated DOCK6 expression was significantly associated with shorter cumulative survival in both univariate and multivariate analyses. Gene ontology analysis of three independent clinical GC cohorts revealed significant involvement of DOCK6-correlated genes in the WNT/β-catenin signaling pathway. Ectopic expression of DOCK6 promoted GC cancer stem cell (CSC) characteristics and chemo- or radioresistance concomitantly through Rac1 activation. Conversely, depletion of DOCK6 suppressed CSC phenotypes and progression of GC, further demonstrating the pivotal role of DOCK6 in GC progression. Our results demonstrate a novel mechanistic link between DOCK6, Rac1, and β-catenin in GCCSC for the first time, supporting the utility of DOCK6 as an independent marker of GC.

Indexed as

Wnt Signaling PathwayAnimalsCell Line, TumorCell MovementCell ProliferationDisease Models, AnimalDisease ProgressionDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticGene SilencingGuanine Nucleotide Exchange FactorsHeterograftsHumansImmunohistochemistryImmunophenotypingMiceDOCK6 protein, humanGuanine Nucleotide Exchange Factors

Identifiers

PMID32753649
OpenAlexW3047395252

What OpenQuestion holds

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Read underepoch 390

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.