» Articles » PMID: 34331382

Expression and Prognostic Potential of PLEK2 in Head and Neck Squamous Cell Carcinoma Based on Bioinformatics Analysis

Overview
Journal Cancer Med
Specialty Oncology
Date 2021 Jul 31
PMID 34331382
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Background: PLEK2 (pleckstrin) could bind to membrane-bound phosphatidylinositols and further promote cell spread. Recently, several studies have noted the importance of PLEK2 in tumor metastasis. However, the role of PLEK2 in head and neck squamous cell carcinoma (HNSCC) remains to be elucidated.

Methods: The PLEK2 expression in HNSCC was identified using Oncomine, Gene Expression Omnibus (GEO), UALCAN databases, and western blot analysis. Prognosis analysis was performed using Kaplan-Meier plotter, DriverDBv3, UALCAN, UCSC Xena, and GEO databases. Single-cell functional analysis was further performed using the cancerSEA database. The PLEK2-related co-expressed genes were identified, and gene set enrichment analysis was performed using LinkedOmics. Furthermore, the top 10 hub genes were identified using the cytoHubba plug-in of Cytoscape. Then, gene enrichment analysis, pathway activity, and drug sensitivity analyses of the hub genes were performed using the R package "clusterProfiler" and GSCAlite. Finally, the UCSC Xena browser was utilized to explore the hub gene most likely to play a synergic role with PLEK2 in HNSCC.

Results: Elevated expression of PLEK2 was observed in HNSCC and even in HNSCC subgroups based on diverse clinicopathological features, portending a poor prognosis in HNSCC. PLEK2 was correlated with metastasis and hypoxia in HNSCC, and the PLEK2-related co-expressed genes were mainly involved in the focal adhesion pathway. The top 10 hub genes were primarily enriched in focal adhesion, HPV infection, ECM-receptor interaction, and PI3K-AKT signaling pathway, and epithelial-mesenchymal transition pathway was activated. Furthermore, the expression levels of the hub genes were associated with sensitivity and resistance to various small molecules and anti-cancer drugs. Further study suggested that ITGA3 and PLEK2 might be viewed as inextricably linked in facilitating HNSCC metastasis.

Conclusions: In general, PLEK2 might serve as a potential biomarker for the diagnosis of HNSCC and guide the development of targeted therapies for HNSCC.

Citing Articles

Upregulation of ENAH by a PI3K/AKT/β-catenin cascade promotes oral cancer cell migration and growth via an ITGB5/Src axis.

Chan X, Chang K, Yang C, Liu C, Hung C, Huang C Cell Mol Biol Lett. 2024; 29(1):136.

PMID: 39511483 PMC: 11545229. DOI: 10.1186/s11658-024-00651-0.


Pleckstrin-2 Mediates the Activation of AKT in Prostate Cancer and Is Repressed by Androgen Receptor.

Han X, Zhang A, Wang P, Bi H, Ren K, Li E Am J Pathol. 2024; 194(10):1986-1996.

PMID: 39069167 PMC: 11423716. DOI: 10.1016/j.ajpath.2024.07.004.


P4HA2 contributes to head and neck squamous cell carcinoma progression and EMT through PI3K/AKT signaling pathway.

Wu Y, Liu W, Zhao T, Jin J Med Oncol. 2024; 41(6):163.

PMID: 38777998 PMC: 11111551. DOI: 10.1007/s12032-024-02358-w.


Analysis of myosin genes in HNSCC and identify MYL1 as a specific poor prognostic biomarker, promotes tumor metastasis and correlates with tumor immune infiltration in HNSCC.

Li C, Guan R, Li W, Wei D, Cao S, Chang F BMC Cancer. 2023; 23(1):840.

PMID: 37679666 PMC: 10486092. DOI: 10.1186/s12885-023-11349-5.


The identification of tumor antigens and immune subtypes based on the development of immunotherapies targeting head and neck squamous cell carcinomas resulting from periodontal disease.

Fu Y, Zheng Y Front Oncol. 2023; 13:1256105.

PMID: 37675228 PMC: 10477783. DOI: 10.3389/fonc.2023.1256105.


References
1.
Zhang W, Li T, Hu B, Li H . Gene Upregulation Might Independently Predict Shorter Progression-Free Survival in Lung Adenocarcinoma. Technol Cancer Res Treat. 2020; 19:1533033820957030. PMC: 7588770. DOI: 10.1177/1533033820957030. View

2.
Chow L . Head and Neck Cancer. N Engl J Med. 2020; 382(1):60-72. DOI: 10.1056/NEJMra1715715. View

3.
Tang Z, Kang B, Li C, Chen T, Zhang Z . GEPIA2: an enhanced web server for large-scale expression profiling and interactive analysis. Nucleic Acids Res. 2019; 47(W1):W556-W560. PMC: 6602440. DOI: 10.1093/nar/gkz430. View

4.
Koshizuka K, Nohata N, Hanazawa T, Kikkawa N, Arai T, Okato A . Deep sequencing-based microRNA expression signatures in head and neck squamous cell carcinoma: dual strands of pre-miR-150 as antitumor miRNAs. Oncotarget. 2017; 8(18):30288-30304. PMC: 5444743. DOI: 10.18632/oncotarget.16327. View

5.
Chandrashekar D, Bashel B, Balasubramanya S, Creighton C, Ponce-Rodriguez I, Chakravarthi B . UALCAN: A Portal for Facilitating Tumor Subgroup Gene Expression and Survival Analyses. Neoplasia. 2017; 19(8):649-658. PMC: 5516091. DOI: 10.1016/j.neo.2017.05.002. View