Author:
Chung Andrew,Guo Jason,Wang Yunguan,Jia Yuemeng,Corbitt Natasha,Li Lin,Wei Yonglong,Zhu Min,Wang Zixi,Guo Holly,Gopal Purva,Xiao Guanghua,Wang Tao,Zhu Hao
Abstract
The origin of cancer is poorly understood because cells that obtain truncal mutations are rarely fate mapped in their native environments. A defining feature of the liver is zonation, or the compartmentalization of metabolic functions in hepatocytes located in distinct regions of the lobule1. However, it is unknown if cancers develop in some zones but not others, and if there are metabolic determinants of cancer risk that track with cellular position. To study cancer initiation, we examined the effect of activating mutations inCtnnb1and loss of function mutations inArid2, two of the most commonly co-mutated genes in hepatocellular carcinoma (HCC)2. We exploited glutamine synthetase (GS) as a faithful fate mapping marker ofCtnnb1mutant hepatocytes. By introducing mutations in distinct zones in a mosaic fashion, we showed that position and metabolic context regulate clone expansion. Mutant clones were maintained in zone 1 but largely outcompeted in zone 3. Paradoxically, clonal maintenance was anti-correlated with cancer initiation, as zone 3 mutant livers showed increased tumorigenesis. To define mechanisms, we individually deleted eleven zone specific genes in HCC mouse models, revealing thatGstm2andGstm3were required for efficient HCC initiation in zone 3. These data indicate that liver cancer initiation is dependent on zonation but independent of clonal expansion.
Publisher
Cold Spring Harbor Laboratory