Evidence map›Paper›PMID 38590195›Full record

ArticleZhongguo fei ai za zhi = Chinese journal of lung cancer2024

[Exploring the Role of PCDHGB4 in the Occurrence of Lung Squamous Cell Carcinoma Based on Bioinformatics Analysis].

Ruijiao Lu, Xieyidai Abuduhailili, Yuxia Li, Jie Ning, Yangchun Feng

Open access · greenAbstract readEnglish Abstract
In one paragraph

Article in Zhongguo fei ai za zhi = Chinese journal of lung cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Ruijiao LuMedical Laboratory Center, The Third Clinical Medical College (Affiliated Cancer Hospital) of
Xinjiang Medical University, Urumqi 830011, China.
Xieyidai AbuduhaililiMedical Laboratory Center, The Third Clinical Medical College (Affiliated Cancer Hospital) of
Xinjiang Medical University, Urumqi 830011, China.
Yuxia LiMedical Laboratory Center, The Third Clinical Medical College (Affiliated Cancer Hospital) of
Xinjiang Medical University, Urumqi 830011, China.
Jie NingMedical Laboratory Center, The Third Clinical Medical College (Affiliated Cancer Hospital) of
Xinjiang Medical University, Urumqi 830011, China.
Yangchun FengMedical Laboratory Center, The Third Clinical Medical College (Affiliated Cancer Hospital) of
Xinjiang Medical University, Urumqi 830011, China.
Xinjiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLung squamous cell carcinoma (LUSC) is a subtypes of non-small cell lung cancer (NSCLC). It has been reported that members of the protocadherin γ family can regulate tumor cell growth by inhibiting the Wnt signaling pathway. Protocadherin-gamma subfamily B4 (PCDHGB4) as a family member in LUSC was rarely reported. The aim of this study was to investigate the role and potential prognostic value of PCDHGB4 in the development of LUSC using bioinformatics methods.

methodsThe Cancer Genome Atlas (TCGA), cBioPortal and UALCAN databases were used to analyze the expression, prognosis, clinicopathological features, immune cell infiltration, immune regulatory genes, immune checkpoint inhibitors (ICIs), and methyltransferases of PCDHGB4 in LUSC. At the single cell level, we analyzed the clustering results of cell subtypes and the expression of PCDHGB4 in different immune cell subpopulations. In addition, we compared the promoter methylation levels of PCDHGB4 in LUSC tissues and normal tissues and performed protein-protein interaction and mutation analysis. Finally, enrichment analysis was performed based on the differentially expressed genes.

resultsBioinformatics analysis results showed that the expression level of PCDHGB4 in LUSC tissues was lower than that in normal tissues. Survival analysis showed that increased PCDHGB4 expression was associated with poor prognosis. Single-cell sequencing analysis showed that PCDHGB4 was expressed in T cells, monocytes or macrophages, and dendritic cells. It was further found that PCDHGB4 played an important role in tumor immunity and confirmed that PCDHGB4 was associated with immune checkpoints, immune regulatory genes, and methyltransferases. Besides, enrichment analysis revealed that PCDHGB4 was involved in multiple cancer-related pathways.

conclusionsThe expression of PCDHGB4 was low in LUSC. PCDHGB4 was related to the poor prognosis of patients, and PCDHGB4 was closely related to the infiltration and pathway of tumor immune cells. PCDHGB4 may be a potential prognostic marker and a new target for immunotherapy in LUSC.

Indexed as

Carcinoma, Non-Small-Cell LungCarcinoma, Squamous CellLung NeoplasmsComputational BiologyGene Expression Regulation, NeoplasticHumansLungMethyltransferasesPrognosisMethyltransferasesLung neoplasmsPCDHGB4Prognosis

Identifiers

PMID38590195
PMCPMC11002194
OpenAlexW4394762477

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LicenceCC BY
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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.