TY - JOUR
T1 - The evolutionary landscape of colorectal tumorigenesis
AU - Cross, William
AU - Kovac, Michal
AU - Mustonen, Ville
AU - Temko, Daniel
AU - Davis, Hayley
AU - Baker, Ann Marie
AU - Biswas, Sujata
AU - Arnold, Roland
AU - Chegwidden, Laura
AU - Gatenbee, Chandler
AU - Anderson, Alexander R.
AU - Koelzer, Viktor H.
AU - Martinez, Pierre
AU - Jiang, Xiaowei
AU - Domingo, Enric
AU - Woodcock, Dan J.
AU - Feng, Yun
AU - Kovacova, Monika
AU - Maughan, Tim
AU - Adams, Richard
AU - Bach, Simon
AU - Beggs, Andrew
AU - Brown, Louise
AU - Buffa, Francesca
AU - Cazier, Jean Baptiste
AU - Domingo, Enric
AU - Blake, Andrew
AU - Wu, Che Hsi
AU - Chatzpili, Ekaterina
AU - Richman, Susan
AU - Dunne, Philip
AU - Harkin, Paul
AU - Higgins, Geoff
AU - Hill, Jim
AU - Holmes, Chris
AU - Horgan, Denis
AU - Kaplan, Rick
AU - Kennedy, Richard
AU - Lawler, Mark
AU - Leedham, Simon
AU - Maughan, Tim
AU - McDermott, Ultan
AU - McKenna, Gillies
AU - Middleton, Gary
AU - Morton, Dion
AU - Murray, Graeme
AU - Quirke, Phil
AU - Salto-Tellez, Manuel
AU - Samuel, Les
AU - Wilson, Richard
AU - The S:CORT Consortium
PY - 2018/8/31
Y1 - 2018/8/31
N2 - The evolutionary events that cause colorectal adenomas (benign) to progress to carcinomas (malignant) remain largely undetermined. Using multi-region genome and exome sequencing of 24 benign and malignant colorectal tumours, we investigate the evolutionary fitness landscape occupied by these neoplasms. Unlike carcinomas, advanced adenomas frequently harbour sub-clonal driver mutations—considered to be functionally important in the carcinogenic process—that have not swept to fixation, and have relatively high genetic heterogeneity. Carcinomas are distinguished from adenomas by widespread aneusomies that are usually clonal and often accrue in a ‘punctuated’ fashion. We conclude that adenomas evolve across an undulating fitness landscape, whereas carcinomas occupy a sharper fitness peak, probably owing to stabilizing selection.
AB - The evolutionary events that cause colorectal adenomas (benign) to progress to carcinomas (malignant) remain largely undetermined. Using multi-region genome and exome sequencing of 24 benign and malignant colorectal tumours, we investigate the evolutionary fitness landscape occupied by these neoplasms. Unlike carcinomas, advanced adenomas frequently harbour sub-clonal driver mutations—considered to be functionally important in the carcinogenic process—that have not swept to fixation, and have relatively high genetic heterogeneity. Carcinomas are distinguished from adenomas by widespread aneusomies that are usually clonal and often accrue in a ‘punctuated’ fashion. We conclude that adenomas evolve across an undulating fitness landscape, whereas carcinomas occupy a sharper fitness peak, probably owing to stabilizing selection.
UR - http://www.scopus.com/inward/record.url?scp=85053310111&partnerID=8YFLogxK
U2 - 10.1038/s41559-018-0642-z
DO - 10.1038/s41559-018-0642-z
M3 - Article
C2 - 30177804
AN - SCOPUS:85053310111
SN - 2397-334X
VL - 2
SP - 1661
EP - 1672
JO - Nature Ecology and Evolution
JF - Nature Ecology and Evolution
IS - 10
ER -