Author:
Tan Qiu Xuan,Shannon Nicholas B.,Lim Weng Khong,Teo Jing Xian,Yap Daniel R. Y.,Lek Sze Min,Tan Joey W. S.,Tan Shih Jia J.,Hendrikson Josephine,Liu Ying,Ng Gillian,Chong Clara Y. L.,Guo Wanyu,Koh Kelvin K. N.,Ng Cedric C. Y.,Rajasegaran Vikneswari,Wong Jolene S.M.,Seo Chin Jin,Ong Choon Kiat,Lim Tony K. H.,Teh Bin Tean,Kon Oi Lian,Chia Claramae S.,Soo Khee Chee,Iyer N. Gopalakrishna,Ong Chin-Ann J.
Abstract
IntroductionField cancerization is suggested to arise from imbalanced differentiation in individual basal progenitor cells leading to clonal expansion of mutant cells that eventually replace the epithelium, although without evidence.MethodsWe performed deep sequencing analyses to characterize the genomic and transcriptomic landscapes of field change in two patients with synchronous aerodigestive tract tumors.ResultsOur data support the emergence of numerous genetic alterations in cancer-associated genes but refutes the hypothesis that founder mutation(s) underpin this phenomenon. Mutational signature analysis identified defective homologous recombination as a common underlying mutational process unique to synchronous tumors.DiscussionOur analyses suggest a common etiologic factor defined by mutational signatures and/or transcriptomic convergence, which could provide a therapeutic opportunity.
Funder
National Medical Research Council