Proteogenomic insights suggest druggable pathways in endometrial carcinoma
Document Type
Article
Publication Date
9-11-2023
Publication Title
Cancer cell
Abstract
We characterized a prospective endometrial carcinoma (EC) cohort containing 138 tumors and 20 enriched normal tissues using 10 different omics platforms. Targeted quantitation of two peptides can predict antigen processing and presentation machinery activity, and may inform patient selection for immunotherapy. Association analysis between MYC activity and metformin treatment in both patients and cell lines suggests a potential role for metformin treatment in non-diabetic patients with elevated MYC activity. PIK3R1 in-frame indels are associated with elevated AKT phosphorylation and increased sensitivity to AKT inhibitors. CTNNB1 hotspot mutations are concentrated near phosphorylation sites mediating pS45-induced degradation of β-catenin, which may render Wnt-FZD antagonists ineffective. Deep learning accurately predicts EC subtypes and mutations from histopathology images, which may be useful for rapid diagnosis. Overall, this study identified molecular and imaging markers that can be further investigated to guide patient stratification for more precise treatment of EC.
Volume
41
Issue
9
First Page
1586
Last Page
1605.e15
Recommended Citation
Dou Y, Katsnelson L, Gritsenko MA, Hu Y, Reva B, Hong R et al [Wilson GD, Pruetz B] Proteogenomic insights suggest druggable pathways in endometrial carcinoma. Cancer Cell. 2023 Sep 11;41(9):1586-1605.e15. doi: 10.1016/j.ccell.2023.07.007. Epub 2023 Aug 10. PMID: 37567170
DOI
10.1016/j.ccell.2023.07.007