Specific Deletions of Chromosomes 3p, 5q, 13q, and 21q among Patients with G2 Grade of Non-Small Cell Lung Cancer

Author:

Kolecka-Bednarczyk Agata1,Frydrychowicz Magdalena1ORCID,Budny Bartłomiej2ORCID,Ruciński Marcin3ORCID,Dompe Claudia14,Gabryel Piotr5ORCID,Płachno Bartosz J.6ORCID,Ruchała Marek2ORCID,Ziemnicka Katarzyna2ORCID,Zieliński Paweł5,Budna-Tukan Joanna37

Affiliation:

1. Department of Immunology, Poznan University of Medical Sciences, 60-806 Poznan, Poland

2. Department of Endocrinology, Metabolism and Internal Medicine, Poznan University of Medical Sciences, 60-355 Poznan, Poland

3. Department of Histology and Embryology, Poznan University of Medical Sciences, 60-781 Poznan, Poland

4. Doctoral School, Poznan University of Medical Sciences, 60-812 Poznan, Poland

5. Department of Thoracic Surgery, Poznan University of Medical Sciences, 60-569 Poznan, Poland

6. Department of Plant Cytology and Embryology, Institute of Botany, Faculty of Biology, Jagiellonian University in Kraków, 30-387 Cracow, Poland

7. Department of Anatomy and Histology, Collegium Medicum, University of Zielona Gora, 65-046 Zielona Gora, Poland

Abstract

Non-small cell lung cancer (NSCLC) leads as a primary cause of cancer-related premature mortality in Western populations. This study leverages cutting-edge gene-expression-profiling technologies to perform an in-depth molecular characterization of NSCLC specimens, with the objective of uncovering tumor-specific genomic alterations. By employing DNA microarray analysis, our research aims to refine the classification of NSCLC for early detection, guide molecular-targeted treatment approaches, enhance prognostication, and broaden the scientific understanding of the disease’s biology. We identified widespread genomic abnormalities in our samples, including the recurrent loss of chromosomal regions 3p, 5q, 13q, and 21q and the gain of 12p. Furthermore, utilizing Metascape for bioinformatic analysis revealed critical biological pathways disrupted in NSCLC, offering promising leads for novel therapeutic interventions.

Publisher

MDPI AG

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