Polo-like Kinase 4: A Multifaceted Marker Linking Tumor Aggressiveness and Unfavorable Prognosis, and Insights into Therapeutic Strategies

Author:

Kim Youngtaek1ORCID,Hwang Joon Yeon1,Kim Dong Kwon23ORCID,Na Kwangmin1,Lee Seul23,Baek Sujeong1,Kang Seong-san4,Yang Seung Min1,Kim Mi Hyun1,Han Heekyung1,Lee Chai Young1,Han Yu Jin1,Hong Min Hee5ORCID,Lee Jii Bum5ORCID,Lim Sun Min5,Cho Byoung Chul56,Park Youngjoon16,Pyo Kyoung-Ho2567ORCID

Affiliation:

1. Department of Research Support, Yonsei Biomedical Research Institute, Yonsei University College of Medicine, Seoul 03186, Republic of Korea

2. Severance Biomedical Science Institutse, Yonsei University College of Medicine, Seoul 03186, Republic of Korea

3. Brain Korea 21 PLUS Project for Medical Science, Yonsei University College of Medicine, Seoul 03186, Republic of Korea

4. JEUK Institute for Cancer Research, JEUK Co., Ltd., Gumi 39418, Republic of Korea

5. Division of Medical Oncology, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul 03186, Republic of Korea

6. Yonsei New Il Han Institute for Integrative Lung Cancer Research, College of Medicine, Yonsei University, Seoul 03186, Republic of Korea

7. Department of Medical Science, College of Medicine, Yonsei University, Seoul 03722, Republic of Korea

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.

Funder

National Research Foundation of Korea

Publisher

MDPI AG

Subject

Cancer Research,Oncology

Reference38 articles.

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