Chromosomal aberrations in Korean nonsmall cell lung carcinomas: degenerate oligonucleotide primed polymerase chain reaction comparative genomic hybridization studies

• Published in: Cancer genetics and cytogenetics 2004-07, Vol.152 (2), p.153-157
• Main Authors: Park, Soo-Yeun, Kim, Yeol-Hong, In, Kwang-Ho, Chun, Yong-Hyuck, Park, Sun-Hwa
• Format: Article
• Language: English
• Subjects: Adenocarcinoma - epidemiology; Adenocarcinoma - genetics; Adenocarcinoma - pathology; Carcinoma, Large Cell - epidemiology; Carcinoma, Large Cell - genetics; Carcinoma, Large Cell - pathology; Carcinoma, Non-Small-Cell Lung - epidemiology; Carcinoma, Non-Small-Cell Lung - genetics; Carcinoma, Non-Small-Cell Lung - pathology; Carcinoma, Squamous Cell - epidemiology; Carcinoma, Squamous Cell - genetics; Carcinoma, Squamous Cell - pathology; Chromosome Aberrations; DNA Primers; DNA, Neoplasm - genetics; Gene Amplification; Gene Dosage; Humans; Korea - epidemiology; Lung Neoplasms - epidemiology; Lung Neoplasms - genetics; Nucleic Acid Hybridization; Polymerase Chain Reaction
• ISSN: 0165-4608; 1873-4456
• DOI: 10.1016/j.cancergencyto.2003.10.016

Chromosomal aberrations were investigated in 48 Korean nonsmall cell carcinomas of the lung (NSCLC), by degenerate oligonucleotide primed polymerase chain reaction comparative genomic hybridization. These included 16 adenocarcinomas, 27 squamous cell carcinomas (SCCs), and 5 large-cell carcinomas. The common sites of copy number increases were 3q26∼qter (23 cases, 48%); 8q23∼qter (46%); 20q13.1 (42%); 1q42∼qter (38%); 3q25 (38%); 21q22 (38%); and 22q13 (38%). DNA amplification was identified in 19 carcinomas (40%), and the frequent sites of amplification were 8q24 (seven cases), 3q26 (seven cases), and 3q27 (seven cases). The frequently under-represented chromosomal regions were Yq (38%), 4q25∼q26 (23%), and 4q31 (23%). In particular, gains of 3q26∼qter (74%), 15q (56%), and 19q (59%) and loss of 13q22∼q31 (26%) were more frequently detected in SCCs of the lung. These nonrandom aberrations can serve as starting points for the identification of potential oncogenes/tumor suppressor genes related to the tumorigenesis of Korean NSCLC.