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Evolutionary characterization of lung adenocarcinoma morphology in TRACERx.


ABSTRACT: Lung adenocarcinomas (LUADs) display a broad histological spectrum from low-grade lepidic tumors through to mid-grade acinar and papillary and high-grade solid, cribriform and micropapillary tumors. How morphology reflects tumor evolution and disease progression is poorly understood. Whole-exome sequencing data generated from 805 primary tumor regions and 121 paired metastatic samples across 248 LUADs from the TRACERx 421 cohort, together with RNA-sequencing data from 463 primary tumor regions, were integrated with detailed whole-tumor and regional histopathological analysis. Tumors with predominantly high-grade patterns showed increased chromosomal complexity, with higher burden of loss of heterozygosity and subclonal somatic copy number alterations. Individual regions in predominantly high-grade pattern tumors exhibited higher proliferation and lower clonal diversity, potentially reflecting large recent subclonal expansions. Co-occurrence of truncal loss of chromosomes 3p and 3q was enriched in predominantly low-/mid-grade tumors, while purely undifferentiated solid-pattern tumors had a higher frequency of truncal arm or focal 3q gains and SMARCA4 gene alterations compared with mixed-pattern tumors with a solid component, suggesting distinct evolutionary trajectories. Clonal evolution analysis revealed that tumors tend to evolve toward higher-grade patterns. The presence of micropapillary pattern and 'tumor spread through air spaces' were associated with intrathoracic recurrence, in contrast to the presence of solid/cribriform patterns, necrosis and preoperative circulating tumor DNA detection, which were associated with extra-thoracic recurrence. These data provide insights into the relationship between LUAD morphology, the underlying evolutionary genomic landscape, and clinical and anatomical relapse risk.

SUBMITTER: Karasaki T 

PROVIDER: S-EPMC7614478 | biostudies-literature | 2023 Apr

REPOSITORIES: biostudies-literature

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Evolutionary characterization of lung adenocarcinoma morphology in TRACERx.

Karasaki Takahiro T   Moore David A DA   Veeriah Selvaraju S   Naceur-Lombardelli Cristina C   Toncheva Antonia A   Magno Neil N   Ward Sophia S   Bakir Maise Al MA   Watkins Thomas B K TBK   Grigoriadis Kristiana K   Huebner Ariana A   Hill Mark S MS   Frankell Alexander M AM   Abbosh Christopher C   Puttick Clare C   Zhai Haoran H   Gimeno-Valiente Francisco F   Saghafinia Sadegh S   Kanu Nnennaya N   Dietzen Michelle M   Pich Oriol O   Lim Emilia L EL   Martínez-Ruiz Carlos C   Black James R M JRM   Biswas Dhruva D   Campbell Brittany B BB   Lee Claudia C   Colliver Emma E   Enfield Katey S S KSS   Hessey Sonya S   Hiley Crispin T CT   Zaccaria Simone S   Litchfield Kevin K   Birkbak Nicolai J NJ   Cadieux Elizabeth Larose EL   Demeulemeester Jonas J   Van Loo Peter P   Adusumilli Prasad S PS   Tan Kay See KS   Cheema Waseem W   Sanchez-Vega Francisco F   Jones David R DR   Rekhtman Natasha N   Travis William D WD   Hackshaw Allan A   Marafioti Teresa T   Salgado Roberto R   Le Quesne John J   Nicholson Andrew G AG   McGranahan Nicholas N   Swanton Charles C   Jamal-Hanjani Mariam M  

Nature medicine 20230412 4


Lung adenocarcinomas (LUADs) display a broad histological spectrum from low-grade lepidic tumors through to mid-grade acinar and papillary and high-grade solid, cribriform and micropapillary tumors. How morphology reflects tumor evolution and disease progression is poorly understood. Whole-exome sequencing data generated from 805 primary tumor regions and 121 paired metastatic samples across 248 LUADs from the TRACERx 421 cohort, together with RNA-sequencing data from 463 primary tumor regions,  ...[more]

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