Integrative analysis of cancer dependency data and comprehensive phosphoproteomics data revealed the EPHA2-PARD3 axis as a cancer vulnerability in KRAS-mutant colorectal cancer

Author:

Gunji Daigo123ORCID,Narumi Ryohei12ORCID,Muraoka Satoshi124ORCID,Isoyama Junko12,Ikemoto Narumi12,Ishida Mimiko12,Tomonaga Takeshi12,Sakai Yoshiharu3ORCID,Obama Kazutaka3ORCID,Adachi Jun1245ORCID

Affiliation:

1. Laboratory of Proteome Research, National Institute of Biomedical Innovation, Health and Nutrition, Osaka, 567-0085, Japan

2. Laboratory of Proteomics for Drug Discovery, Center for Drug Design Research, National Institute of Biomedical Innovation, Health and Nutrition, Osaka, 567-0085, Japan

3. Department of Surgery, Kyoto University Graduate School of Medicine Faculty of Medicine, Kyoto, 606-8507, Japan

4. Laboratory of Clinical and Analytical Chemistry, Center for Drug Design Research, National Institute of Biomedical Innovation, Health and Nutrition, Osaka, 567-0085, Japan

5. Laboratory of Proteomics and Drug Discovery, Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto, 606-8501, Japan

Abstract

The phosphoproteomics landscape of 35 CRC cell lines revealed unique molecular characteristics of KRAS-mutant cells.Integrated analysis with gene-dependency data identified vulnerability signals in KRAS-mutant cancers.

Funder

Japan Society for the Promotion of Science

Publisher

Royal Society of Chemistry (RSC)

Subject

Genetics,Molecular Biology,Biochemistry

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