AUTHOR=Han Xiaohong , Tan Qiaoyun , Yang Sheng , Li Junling , Xu Jianping , Hao Xuezhi , Hu Xingsheng , Xing Puyuan , Liu Yutao , Lin Lin , Gui Lin , Qin Yan , Yang Jianliang , Liu Peng , Wang Xingyuan , Dai Wumin , Lin Dongmei , Lin Hua , Shi Yuankai 

TITLE=Comprehensive Profiling of Gene Copy Number Alterations Predicts Patient Prognosis in Resected Stages I–III Lung Adenocarcinoma

JOURNAL=Frontiers in Oncology

VOLUME=9

YEAR=2019

URL=https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2019.00556

DOI=10.3389/fonc.2019.00556

ISSN=2234-943X

ABSTRACT=<p><bold>Background:</bold> Lung adenocarcinoma (LUAD) possesses a poor prognosis with a low 5-year survival rate even for stages I-III resected patients, it is thus critical to understand the determinants that affect the survival and discover new potentially prognostic biomarkers. Somatic copy number alterations (CNAs) are major source of genomic variations driving tumor evolution, CNAs screening may identify prognostic biomarkers.</p><p><bold>Methods:</bold> Oncoscan MIP array was used to analyze the patterns of CNAs on formalin fixed paraffin embedded(FFPE) tumor specimens from 163 consecutive stage I-III resected LUAD patients, 145 out of which received platinum-based adjuvant chemotherapy.</p><p><bold>Results:</bold> Of the 163 patients, 91(55.8%) were recurred within 3 years after surgery. The most common aberrations in our cohort were 1q, 5p, 5q, 7p, 8q, 14p, 16p, 17q, 20q for copy number gains and 8p, 9p, 13p, 16q, 18q for losses. The GISTIC2 analysis produced 45 amplification peaks and 40 deletion peaks, involving some reported genes <italic>TERT, EGFR, MYC, CCND1, CDK4, MDM2, ERBB2, NKX2-1, CCNE1</italic>, and <italic>CDKN2A</italic>, most of which were consistent with TCGA database. The amplifications of 12p12.1 (<italic>CMAS, GOLT1B, YS2, LDHB, RECQL, ETNK1, IAPP, PYROXD1, KRAS</italic>) and <italic>KDM5A</italic> were correlated with worse prognosis in our cohort, this result was further validated in 506 LUAD patients from TCGA. In addition, 163 patients could be well-classified into five groups, and the clinical outcomes were significantly different based on threshold copy number at reoccurring alteration peaks. Among the 145 patients who received adjuvant chemotherapy, focal amplification of <italic>ERBB2</italic> and deletion of 4q34.3 were found to be specific in relapsed patients, this result was validated in an independent group of Imielinski et al., demonstrating these two CNAs may contribute to resected LUAD recurrence after adjuvant chemotherapy.</p><p><bold>Conclusion:</bold> This study suggests that CNAs profiling may be a potential prognostic classifier in resected LAUD patients. Amplifications of 12p12.1 and <italic>KDM5A</italic> might be prognostic biomarkers for LUAD, and amplification of <italic>ERBB2</italic> and deletion of 4q34.3 predicted early relapse after adjuvant chemotherapy. These novel findings may provide implication for better implementation of precision therapy for lung cancer patients.</p>