Evidence map›Paper›PMID 31450490›Full record

ArticleCancer biomarkers : section A of Disease markers2019

PCDH20 acts as a tumour-suppressor gene through the Wnt/β-catenin signalling pathway in hypopharyngeal squamous cell carcinoma.

Zhitao Gong, Guohua Hu

Abstract read
In one paragraph

Article in Cancer biomarkers : section A of Disease markers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
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  3. ZNF714 Supports Pro-Oncogenic Features in Lung Cancer Cells.International journal of molecular sciences · 2023
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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Zhitao Gong
Guohua Hu

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDownregulation of PCDH20 is frequently involved in tumorigenesis of many cancers, but the role of PCDH20 protein in hypopharyngeal squamous cell carcinoma (HSCC) is still unknown.

objectiveThe aim of this study was to investigate the role of PCDH20 in hypopharyngeal squamous cell carcinoma (HSCC).

methodsImmunohistochemistry (IHC) and qRT-PCR was carried out to estimate the expressions of PCDH20 protein and mRNA in HSCC tissues and adjacent non-tumor tissues. Correlation between the PCDH20 expression and clinicopathological characteristics was evaluated using chi-square test. Meanwhile, Kaplan-Meier method and log-rank test were applied to analyze the overall survival. After transfection of PCDH20, the CCK8 assay, Cell migration assay and invasion assay were used to investigate the changes in the viability, migration and invasion of Fuda cells. The mechanisms by which reduced PCDH20 promote migration and invasion of Fuda cells were examined using western blotting.

resultsPCDH20 protein showed in tumor tissue low expression rates of 67.5% (54/80). The mRNA of PCDH20 indicated the consistent trend (80%, 8/10). Reduced PCDH20 expression was positively related to T stage and lymph node metastasis (P< 0.05). Patients with low levels of PCDH20 had worse overall survival compared with those with high PCDH20 levels (P< 0.001). The univariate Cox regression analysis described that lymph node metastasis (P= 0.043) and down-regulated PCDH20 expression (P= 0.045) were significantly prognostic factors.Multivariate analysis suggested that low PCDH20 expression (P= 0.015) were significantly independent prognostic factors for overall survival. PCDH20 in Fadu cells significantly inhibited cell viability, migration and invasion. Meanwhile, PCDH20 was involved in the disruption of HSCC progression through antagonizing its downstream Wnt/β-catenin signalling pathway.

conclusionOur data highlight that the downregulated PCDH20 may serve as reliable diagnostic biomarker in HSCC.

Indexed as

Gene Expression Regulation, NeoplasticWnt Signaling PathwayApoptosisBiomarkers, TumorCadherinsCarcinoma, Squamous CellCell MovementCell ProliferationFemaleFollow-Up StudiesHumansHypopharyngeal NeoplasmsLymphatic MetastasisMaleMiddle AgedNeoplasm InvasivenessBiomarkers, TumorCadherinsNerve Tissue ProteinsPCDH20 protein, humanProtocadherinsclinicopathological featureshypopharyngeal squamous cell carcinomalymph node metastasisPCDH20prognostic

Identifiers

PMID31450490
PMCPMC12826438
OpenAlexW2969546228

What OpenQuestion 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 OpenQuestion graph.