Specific Deletions of Chromosomes 3p, 5q, 13q, and 21q among Patients with G2 Grade of Non-Small Cell Lung Cancer.
Agata Kolecka-BednarczykMagdalena FrydrychowiczBartłomiej BudnyMarcin RucinskiClaudia DompePiotr GabryelBartosz Jan PłachnoMarek RuchalaMasehullah SadiqiPaweł ZielińskiJoanna Budna-TukanPublished in: International journal of molecular sciences (2024)
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.
Keyphrases
- small cell lung cancer
- advanced non small cell lung cancer
- copy number
- genome wide
- brain metastases
- physical activity
- cardiovascular disease
- south africa
- type diabetes
- cardiovascular events
- risk factors
- gene expression
- single cell
- dna methylation
- epidermal growth factor receptor
- cancer therapy
- optical coherence tomography
- circulating tumor
- smoking cessation