Genomic comparison of esophageal squamous cell carcinoma and its precursor lesions by multi-region whole-exome sequencing

Esophageal squamous dysplasia is believed to be the precursor lesion of esophageal squamous cell carcinoma (ESCC); however, the genetic evolution from dysplasia to ESCC remains poorly understood. Here, we applied multi-region whole-exome sequencing to samples from two cohorts, 45 ESCC patients with matched dysplasia and carcinoma samples, and 13 tumor-free patients with only dysplasia samples. Our analysis reveals that dysplasia is heavily mutated and harbors most of the driver events reported in ESCC. Moreover, dysplasia is polyclonal, and remarkable heterogeneity is often observed between tumors and their neighboring dysplasia samples. Notably, copy number alterations are prevalent in dysplasia and persist during the ESCC progression, which is distinct from the development of esophageal adenocarcinoma. The sharp contrast in the prevalence of the 'two-hit' event on TP53 between the two cohorts suggests that the complete inactivation of TP53 is essential in promoting the development of ESCC.National Key RD Program [2017YFA0505600-04]; Ministry of Science and Technology of China [2015AA020403, 2015AA020931]; National Key Research and Development Program [2016YFC0900100]; National Natural Science Foundation of China [81230045, 91440106, 81572403, 81572600, 31370847, 31327901]; Beijing Municipal Science & Technology Commission [Z141100000214013]; Recruitment Program of Global Youth Experts; Science and Technology project of Guangdong Province [2014B050504004, 2015B050501005]; talent program of Guangdong Province [412022693047]SCI(E)ARTICLE