Deep sequencing reveals the genomic characteristics of lung adenocarcinoma presenting as ground-glass nodules (GGNs)

被引:12
作者
Wu, Nan [1 ]
Liu, Sixue [2 ,3 ]
Li, Jingjing [4 ]
Hu, Zhenyu [2 ,3 ]
Yan, Shi [1 ]
Duan, Hongwei [2 ,3 ]
Wu, Dafei [2 ,5 ]
Ma, Yuanyuan [1 ]
Li, Shaolei [1 ]
Wang, Xing [1 ]
Wang, Yaqi [1 ]
Li, Xiang [1 ]
Lu, Xuemei [2 ,3 ,6 ]
机构
[1] Peking Univ Canc Hosp & Inst, Dept Thorac Surg 2, Key Lab Carcinogenesis & Translat Res, Minist Educ, Beijing, Peoples R China
[2] Chinese Acad Sci, Beijing Inst Genom, Key Lab Genom & Precis Med, Beijing, Peoples R China
[3] Univ Chinese Acad Sci, Beijing, Peoples R China
[4] Nanjing Univ, Drum Tower Hosp, Med Sch, Precis Med Ctr, Nanjing, Peoples R China
[5] Chinese Acad Sci, Inst Zool, Key Lab Zool Systemat & Evolut, Beijing, Peoples R China
[6] Chinese Acad Sci, CAS Ctr Excellence Anim Evolut & Genet, Kunming, Yunnan, Peoples R China
基金
国家重点研发计划; 北京市自然科学基金;
关键词
Ground-glass nodules (GGNs); lung adenocarcinoma (LUAD); deep sequencing; genomic analysis; COPY-NUMBER ALTERATION; MUTATIONAL HETEROGENEITY; COMPUTED-TOMOGRAPHY; CANCER GENOME; OPACITY; ASSOCIATION; CT; CLASSIFICATION; INSTABILITY; SENSITIVITY;
D O I
10.21037/tlcr-20-1086
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The concept of multi-step progression from atypical adenomatous hyperplasia (AAH) to invasive adenocarcinoma (ADC) has been proposed, and ground-glass nodules (GGNs) may play a critical role during the early lung tumorigenesis. We present the first comprehensive description of the genomic architecture of GGNs to unravel the genetic basis of GGN. Methods: We investigated 30 GGN-like lungs ADC by performing >1,000x whole-exome sequencing (WES) and characterized the genomic variations and evaluate the relationship between the clinicopathologic and molecular characteristics in this disease. Results: Despite the low somatic mutation burden, GGNs exhibited high intratumor heterogeneity (ITH) characterized by the proportion of subclonal mutations. Different mutagenesis shaped the genomes of GGN during cancer evolution and were mostly featured by molecular clock-like signatures that occur in clonal mutations and defective DNA mismatch signatures that occur in subclonal mutations. Moreover, 10.7-67.1% clonal mutations occurred after whole-genome doubling (WGD), indicating that WGD could be a frequent truncal event in GGNs. Samples with WGD showed higher genomic instability but lower ITH. These GGNs were characterized by recurrent focal copy-number changes that are highly associated with tumorigenesis, with only two genes (EGFR and RBM10) that were recurrently mutated. Additionally, GGNs with different pathological subtypes or computed tomography (CT) features exhibited distinct genetic characteristics. Lepidic predominant or pure GGNs in CT images carried a lower mutation burden and had a relatively stable genome than nonlepidic or mixed GGNs. GGNs with RBM10 mutations tended to accompany a pathologically lepidic pattern, indicating RBM10 may drive the distinct subtype of lung cancer with better prognosis. Conclusions: These findings facilitated interpreting the genomic characteristics of GGNs, provided insight into the early stages of lung cancer evolution, and possessed potential clinical significance.
引用
收藏
页码:1239 / +
页数:22
相关论文
共 70 条
[1]   Global surveillance of trends in cancer survival 2000-14 (CONCORD-3): analysis of individual records for 37 513 025 patients diagnosed with one of 18 cancers from 322 population-based registries in 71 countries [J].
Allemani, Claudia ;
Matsuda, Tomohiro ;
Di Carlo, Veronica ;
Harewood, Rhea ;
Matz, Melissa ;
Niksic, Maja ;
Bonaventure, Audrey ;
Valkov, Mikhail ;
Johnson, Christopher J. ;
Esteve, Jacques ;
Ogunbiyi, Olufemi J. ;
Azevedo e Silva, Gulnar ;
Chen, Wan-Qing ;
Eser, Sultan ;
Engholm, Gerda ;
Stiller, Charles A. ;
Monnereau, Alain ;
Woods, Ryan R. ;
Visser, Otto ;
Lim, Gek Hsiang ;
Aitken, Joanne ;
Weir, Hannah K. ;
Coleman, Michel P. .
LANCET, 2018, 391 (10125) :1023-1075
[2]   The landscape of somatic copy-number alteration across human cancers [J].
Beroukhim, Rameen ;
Mermel, Craig H. ;
Porter, Dale ;
Wei, Guo ;
Raychaudhuri, Soumya ;
Donovan, Jerry ;
Barretina, Jordi ;
Boehm, Jesse S. ;
Dobson, Jennifer ;
Urashima, Mitsuyoshi ;
Mc Henry, Kevin T. ;
Pinchback, Reid M. ;
Ligon, Azra H. ;
Cho, Yoon-Jae ;
Haery, Leila ;
Greulich, Heidi ;
Reich, Michael ;
Winckler, Wendy ;
Lawrence, Michael S. ;
Weir, Barbara A. ;
Tanaka, Kumiko E. ;
Chiang, Derek Y. ;
Bass, Adam J. ;
Loo, Alice ;
Hoffman, Carter ;
Prensner, John ;
Liefeld, Ted ;
Gao, Qing ;
Yecies, Derek ;
Signoretti, Sabina ;
Maher, Elizabeth ;
Kaye, Frederic J. ;
Sasaki, Hidefumi ;
Tepper, Joel E. ;
Fletcher, Jonathan A. ;
Tabernero, Josep ;
Baselga, Jose ;
Tsao, Ming-Sound ;
Demichelis, Francesca ;
Rubin, Mark A. ;
Janne, Pasi A. ;
Daly, Mark J. ;
Nucera, Carmelo ;
Levine, Ross L. ;
Ebert, Benjamin L. ;
Gabriel, Stacey ;
Rustgi, Anil K. ;
Antonescu, Cristina R. ;
Ladanyi, Marc ;
Letai, Anthony .
NATURE, 2010, 463 (7283) :899-905
[3]   MutationalPatterns: comprehensive genome-wide analysis of mutational processes [J].
Blokzijl, Francis ;
Janssen, Roel ;
van Boxtel, Ruben ;
Cuppen, Edwin .
GENOME MEDICINE, 2018, 10
[4]  
Bray F, 2018, CA-CANCER J CLIN, V68, P394, DOI [10.3322/caac.21492, 10.3322/caac.21609]
[5]   Hepatic Stem-like Phenotype and Interplay of Wnt/β-Catenin and Myc Signaling in Aggressive Childhood Liver Cancer [J].
Cairo, Stefano ;
Armengol, Carolina ;
De Reynies, Auelien ;
Wei, Yu ;
Thomas, Emilie ;
Renard, Claire-Angelique ;
Goga, Andrei ;
Balakrishnan, Asha ;
Semeraro, Michaela ;
Gresh, Lionel ;
Pontoglio, Marco ;
Strick-Marchand, Helene ;
Levillayer, Florence ;
Nouet, Yann ;
Rickman, David ;
Gauthier, Frederic ;
Branchereau, Sophie ;
Brugieres, Laurence ;
Laithier, Veronique ;
Bouvier, Raymonde ;
Boman, Francoise ;
Basso, Giuseppe ;
Michiels, Jean-Francois ;
Hofman, Paul ;
Arbez-Gindre, Francine ;
Jouan, Helene ;
Chapeau, Marie-Christine Rousselet ;
Berrebi, Dominique ;
Marcellin, Luc ;
Plenat, Francois ;
Zachar, Dominique ;
Joubert, Madeleine ;
Selves, Janick ;
Pasquier, Dominique ;
Bioulac-Sage, Paulette ;
Grotzer, Michael ;
Childs, Margaret ;
Fabre, Monique ;
Buendia, Marie-Annick .
CANCER CELL, 2008, 14 (06) :471-484
[6]  
Cancer Genome Atlas Research Network, 2018, Nature, V559, pE12, DOI [10.1038/nature13385, 10.1038/s41586-018-0228-6]
[7]   Absolute quantification of somatic DNA alterations in human cancer [J].
Carter, Scott L. ;
Cibulskis, Kristian ;
Helman, Elena ;
McKenna, Aaron ;
Shen, Hui ;
Zack, Travis ;
Laird, Peter W. ;
Onofrio, Robert C. ;
Winckler, Wendy ;
Weir, Barbara A. ;
Beroukhim, Rameen ;
Pellman, David ;
Levine, Douglas A. ;
Lander, Eric S. ;
Meyerson, Matthew ;
Getz, Gad .
NATURE BIOTECHNOLOGY, 2012, 30 (05) :413-+
[8]   Mutational Landscape and Sensitivity to Immune Checkpoint Blockers [J].
Chabanon, Roman M. ;
Pedrero, Marion ;
Lefebvre, Celine ;
Marabelle, Aurelien ;
Soria, Jean-Charles ;
Postel-Vinay, Sophie .
CLINICAL CANCER RESEARCH, 2016, 22 (17) :4309-4321
[9]   Natural History of Pure Ground-Glass Opacity Lung Nodules Detected by Low-Dose CT Scan [J].
Chang, Boksoon ;
Hwang, Jung Hye ;
Choi, Yoon-Ho ;
Chung, Man Pyo ;
Kim, Hojoong ;
Kwon, O. Jung ;
Lee, Ho Yun ;
Lee, Kyung Soo ;
Shim, Young Mog ;
Han, Joungho ;
Um, Sang-Won .
CHEST, 2013, 143 (01) :172-178
[10]   Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples [J].
Cibulskis, Kristian ;
Lawrence, Michael S. ;
Carter, Scott L. ;
Sivachenko, Andrey ;
Jaffe, David ;
Sougnez, Carrie ;
Gabriel, Stacey ;
Meyerson, Matthew ;
Lander, Eric S. ;
Getz, Gad .
NATURE BIOTECHNOLOGY, 2013, 31 (03) :213-219