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韩国非小细胞肺癌中的染色体畸变:简并寡核苷酸引物聚合酶链反应比较基因组杂交研究

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

作者信息

Park Soo-Yeun, Kim Yeol-Hong, In Kwang-Ho, Chun Yong-Hyuck, Park Sun-Hwa

机构信息

Department of Anatomy, Medical Research Center, College of Medicine, Ewha Womans University, 911-1 Mok Dong, Yangcheon-Gu, Seoul, Korea.

出版信息

Cancer Genet Cytogenet. 2004 Jul 15;152(2):153-7. doi: 10.1016/j.cancergencyto.2003.10.016.

Abstract

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 approximately qter (23 cases, 48%); 8q23 approximately qter (46%); 20q13.1 (42%); 1q42 approximately 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 approximately q26 (23%), and 4q31 (23%). In particular, gains of 3q26 approximately qter (74%), 15q (56%), and 19q (59%) and loss of 13q22 approximately 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.

摘要

通过简并寡核苷酸引物聚合酶链反应比较基因组杂交技术,对48例韩国非小细胞肺癌(NSCLC)进行了染色体畸变研究。其中包括16例腺癌、27例鳞状细胞癌(SCC)和5例大细胞癌。拷贝数增加的常见位点为3q26至qter(23例,48%);8q23至qter(46%);20q13.1(42%);1q42至qter(38%);3q25(38%);21q22(38%);以及22q13(38%)。在19例癌(40%)中鉴定出DNA扩增,扩增的常见位点为8q24(7例)、3q26(7例)和3q27(7例)。染色体区域常见的低表达区域为Yq(38%)、4q25至q26(23%)和4q31(23%)。特别是,在肺SCC中更频繁地检测到3q26至qter(74%)、15q(56%)和19q(59%)的增益以及13q22至q31(26%)的缺失。这些非随机畸变可作为鉴定与韩国NSCLC肿瘤发生相关的潜在癌基因/肿瘤抑制基因的起点。

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