Home CAS Center for Excellence
Media Reports
Address: 320 Yue Yang Road, Shanghai 200031, P.R. China
Tel: 86-21-54920000
Fax: 86-21-54921011
Email: sibcb@sibs.ac.cn
Website: www.sibcb.ac.cn
In vivo CRISPR screening unveils important tumor suppressor gene in lung tumorigenesis
Viewed: 103

Research teams led by Dr. JI Hongbin at the Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences and Dr. CHEN Liang at the Institute of Life and Health Engineering, Jinan University provide a systematic CRISPR screening of tumor suppressor genes (TSGs) in vivo and demonstrate UTX functions as the important epigenetic regulator in lung tumorigenesis.

Cancer genomic studies have provided a comprehensive spectrum of thousands of potentially important genetic alterations of TSGs. Except for a few well-studied TSGs, most of these genetic aberrations still remain to be functionally validated and characterized. Given the emergence of a tremendous amount of cancer genomic alterations, traditional methods, such as the genetically engineered mouse models (GEMMs), clearly could not meet the demand. The clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 system has been proven to be a powerful genome editing tool in recent years. Thus, this type of somatic gene knockout technique makes it feasible to efficiently and systematically identify potential TSGs in vivo.

In this current study, researchers first generated a list of potential TSG candidates based on integrative bioinformatics analyses. Taking advantage of the CRISPR/Cas9-mediated screening in vivo technique, multiple TSGs including Utx, Ptip, Acp5, Acacb, and Clu were identified for their contribution to lung cancer malignant progression. All these genes were frequently down-regulated in human lung cancer specimens and significantly associated with lung cancer patient survival. Importantly, conditional knockout of the histone demethylase Utx dramatically accelerated lung tumorigenesis in the KrasLSL-G12D/+ mouse model. Further evidences demonstrated Utx knockout increased H3K27me3 level potentially through EZH2 upregulation. Moreover, researchers found a treatment strategy for UTX-deficient lung tumors. The EZH2 inhibitor JQEZ5 preferentially suppresses the growth of Utx-knockout lung tumors, providing therapeutic implication for human lung cancer with KRAS mutations exhibiting low UTX level.

The paper entitled “In vivo CRISPR screening unveils histone demethylase UTX as an important epigenetic regulator in lung tumorigenesis” was published online in Proc Natl Acad Sci USA. on April 9, 2018. This study was supported by the National Basic Research Program of China, Strategic Priority Research Program of the Chinese Academy of Sciences, National Natural Science Foundation of China, Science and Technology Commission of Shanghai Municipality, China Postdoctoral Science Foundation, Chinese Academy of Science Taiwan Young Scholar Visiting Program, Science and Technology Program of Guangzhou and National Key R&D Program of China.

Dr. JI Hongbin 
Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, Shanghai, China
Email: hbji@sibcb.ac.cn

Dr. CHEN Liang 
Institute of Life and Health Engineering, Jinan University, Guangzhou, China
Email: chenliang@nibs.ac.cn


Copyright © 2017-2020 Shanghai Institute of Biochemistry and Cell Biology, CAS. All rights reserved