Author/Authors :
Lars Zender، نويسنده , , Wen Xue، نويسنده , , Johannes Zuber، نويسنده , , Camile P. Semighini، نويسنده , , Alexander Krasnitz، نويسنده , , Beicong Ma، نويسنده , , Peggy Zender، نويسنده , , Stefan Kubicka، نويسنده , , John M. Luk، نويسنده , , Peter Schirmacher، نويسنده , , W. Richard McCombie، نويسنده , , Michael Wigler، نويسنده , , James Hicks، نويسنده , , Gregory J. Hannon، نويسنده , , Scott Powers، نويسنده , , Scott W. Lowe، نويسنده ,
Abstract :
Cancers are highly heterogeneous and contain many passenger and driver mutations. To functionally identify tumor suppressor genes relevant to human cancer, we compiled pools of short hairpin RNAs (shRNAs) targeting the mouse orthologs of genes recurrently deleted in a series of human hepatocellular carcinomas and tested their ability to promote tumorigenesis in a mosaic mouse model. In contrast to randomly selected shRNA pools, many deletion-specific pools accelerated hepatocarcinogenesis in mice. Through further analysis, we identified and validated 13 tumor suppressor genes, 12 of which had not been linked to cancer before. One gene, XPO4, encodes a nuclear export protein whose substrate, EIF5A2, is amplified in human tumors, is required for proliferation of XPO4-deficient tumor cells, and promotes hepatocellular carcinoma in mice. Our results establish the feasibility of in vivo RNAi screens and illustrate how combining cancer genomics, RNA interference, and mosaic mouse models can facilitate the functional annotation of the cancer genome.
