Wnt信号通路
斑马鱼
脂质代谢
癌变
生物
转录组
转基因
细胞生物学
LRP6型
脂肪变性
转基因小鼠
信号转导
癌症研究
癌症
内分泌学
生物化学
基因表达
遗传学
基因
作者
Yuxiao Yao,Shaoyang Sun,Li Wang,Fei Fei,Zhao‐Ru Dong,Ai‐Wu Ke,Ruoyu He,Lei Wang,Lili Zhang,Minbiao Ji,Qiang Li,Min Yu,Guo‐Ming Shi,Jia Fan,Zhiyuan Gong,Xu Wang
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2018-10-01
卷期号:78 (19): 5548-5560
被引量:51
标识
DOI:10.1158/0008-5472.can-17-3964
摘要
Abstract There is limited understanding of the effects of major oncogenic pathways and their combinatorial actions on lipid composition and transformation during hepatic tumorigenesis. Here, we report a negative correlation of Wnt/Myc activity with steatosis in human hepatocellular carcinoma (HCC) and perform in vivo functional studies using three conditional transgenic zebrafish models. Double-transgenic zebrafish larvae conditionally expressing human CTNNB1mt and zebrafish tcf7l2 or murine Myc together with krasv12 in hepatocytes led to severe hepatomegaly and significantly attenuated accumulation of lipid droplets and cell senescence triggered by krasv12 expression alone. UPLC-MS–based, nontargeted lipidomic profiling and transcriptome analyses revealed that Wnt/Myc activity promotes triacylglycerol to phospholipid transformation and increases unsaturated fatty acyl groups in phospholipids in a Ras-dependent manner. Small-scale screenings suggested that supplementation of certain free fatty acids (FA) or inhibition of FA desaturation significantly represses hepatic hyperplasia of double-transgenic larvae and proliferation of three human HCC cells with and without sorafenib. Together, our studies reveal novel Ras-dependent functions of Wnt signaling in remodeling the lipid metabolism of cancerous hepatocytes in zebrafish and identify the SCD inhibitor MK8245 as a candidate drug for therapeutic intervention. Significance: These findings identify FA desaturation as a significant downstream therapeutic target for antagonizing the combinatorial effects of Wnt and Ras signaling pathways in hepatocellular carcinoma. Graphical Abstract: http://cancerres.aacrjournals.org/content/canres/78/19/5548/F1.large.jpg. Cancer Res; 78(19); 5548–60. ©2018 AACR.
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