Genome-wide CRISPR screens in spheroid culture reveal that the tumor suppressor LKB1 inhibits growth via the PIKFYVE lipid kinase

Author:

Ferrarone John R.12ORCID,Thomas Jerin1,Unni Arun M.1,Zheng Yuxiang1,Nagiec Michal J.13,Gardner Eric E.1,Mashadova Oksana1,Li Kate1,Koundouros Nikos13,Montalbano Antonino45,Mustafa Meer45,Cantley Lewis C.16ORCID,Blenis John13ORCID,Sanjana Neville E.45ORCID,Varmus Harold16ORCID

Affiliation:

1. Meyer Cancer Center, Weill Cornell Medicine, New York, NY 10021

2. Division of Hematology and Medical Oncology, Department of Medicine, Weill Cornell Medicine, New York, NY 10021

3. Department of Pharmacology, Weill Cornell Medicine, New York, NY 10021

4. New York Genome Center, New York, NY 10013

5. Department of Biology, New York University, New York, NY 10003

6. Department of Medicine, Weill Cornell Medicine, New York, NY 10021

Abstract

The tumor suppressor LKB1 is a serine/threonine protein kinase that is frequently mutated in human lung adenocarcinoma (LUAD). LKB1 regulates a complex signaling network that is known to control cell polarity and metabolism; however, the pathways that mediate the tumor-suppressive activity of LKB1 are incompletely defined. To identify mechanisms of LKB1-mediated growth suppression, we developed a spheroid-based cell culture assay to study LKB1-dependent growth. We then performed genome-wide CRISPR screens in spheroidal culture and found that LKB1 suppresses growth, in part, by activating the PIKFYVE lipid kinase. Finally, we used chemical inhibitors and a pH-sensitive reporter to determine that LKB1 impairs growth by promoting the internalization of wild-type EGFR in a PIKFYVE-dependent manner.

Funder

Damon Runyon Cancer Research Foundation

HHS | NIH | NCI | CCR | Basic Research Laboratory

HHS | NIH | National Human Genome Research Institute

Publisher

Proceedings of the National Academy of Sciences

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