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Polo-like Kinase 4: A Multifaceted Marker Linking Tumor Aggressiveness and Unfavorable Prognosis, and Insights into Therapeutic Strategies
SIMPLE SUMMARY: Polo-like kinase 4 (PLK4) is associated with tumorigenesis and prognosis in various types of cancer. Prognostic analysis of PLK4 expression and data analysis of its association with the somatic mutation and drug resistance through clustering were performed using the Cancer Genome Atl...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10526937/ https://www.ncbi.nlm.nih.gov/pubmed/37760631 http://dx.doi.org/10.3390/cancers15184663 |
Sumario: | SIMPLE SUMMARY: Polo-like kinase 4 (PLK4) is associated with tumorigenesis and prognosis in various types of cancer. Prognostic analysis of PLK4 expression and data analysis of its association with the somatic mutation and drug resistance through clustering were performed using the Cancer Genome Atlas-lung adenocarcinoma (TCGA-LUAD) dataset. According to these results, PLK4 expression is associated with poor prognosis, TP53 mutations, and drug resistance in patients with LUAD. ABSTRACT: (1) Background: This study investigated whether polo-like kinase 4 (PLK4) is a suitable therapeutic target or biomarker for lung adenocarcinoma (LUAD). (2) Methods: We acquired LUAD data from The Cancer Genome Atlas (TCGA) database through the UCSC Xena data portal. Gene expression, clinical, survival, and mutation data from multiple samples were analyzed. Gene enrichment analysis, unsupervised clustering of PLK4-related pathways, and differential gene expression analyses were performed. Additionally, correlations, t-tests, survival analyses, and statistical analyses were performed. (3) Results: PLK4 expression was higher in LUAD tissues than in normal tissues and was associated with poor prognosis for both overall and progression-free survival in LUAD. PLK4 was highly correlated with cell-proliferation-related pathways using Gene Ontology (GO) biological process terms. PLK4 expression and pathways that were highly correlated with PLK4 expression levels were upregulated in patients with LUAD with the TP53 mutation. (4) Conclusions: PLK4 expression affects the survival of patients with LUAD and is a potential therapeutic target for LUAD with TP53 mutations. |
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