Back to Search Start Over

Cyclin Dependent Kinase Inhibitor 2A Genetic and Epigenetic Alterations Interfere with Several Immune Components and Predict Poor Clinical Outcome.

Authors :
Soltan MA
Alhanshani AA
Shati AA
Alqahtani YA
Alshaya DS
Alharthi J
Altalhi SA
Fayad E
Zaki MSA
Eid RA
Source :
Biomedicines [Biomedicines] 2023 Aug 11; Vol. 11 (8). Date of Electronic Publication: 2023 Aug 11.
Publication Year :
2023

Abstract

Cyclin dependent kinase inhibitor 2A (CDKN2A) is a well-known tumor suppressor gene as it functions as a cell cycle regulator. While several reports correlate the malfunction of CDKN2A with the initiation and progression of several types of human tumors, there is a lack of a comprehensive study that analyzes the potential effect of CDKN2A genetic alterations on the human immune components and the consequences of that effect on tumor progression and patient survival in a pan-cancer model. The first stage of the current study was the analysis of CDKN2A differential expression in tumor tissues and the corresponding normal ones and correlating that with tumor stage, grade, metastasis, and clinical outcome. Next, a detailed profile of CDKN2A genetic alteration under tumor conditions was described and assessed for its effect on the status of different human immune components. CDKN2A was found to be upregulated in cancerous tissues versus normal ones and that predicted the progression of tumor stage, grade, and metastasis in addition to poor prognosis under different forms of tumors. Additionally, CDKN2A experienced different forms of genetic alteration under tumor conditions, a characteristic that influenced the infiltration and the status of CD8, the chemokine CCL4, and the chemokine receptor CCR6. Collectively, the current study demonstrates the potential employment of CDKN2A genetic alteration as a prognostic and immunological biomarker under several types of human cancers.

Details

Language :
English
ISSN :
2227-9059
Volume :
11
Issue :
8
Database :
MEDLINE
Journal :
Biomedicines
Publication Type :
Academic Journal
Accession number :
37626750
Full Text :
https://doi.org/10.3390/biomedicines11082254