| Literature DB >> 36248745 |
Supawan Jamnongsong1, Patipark Kueanjinda1,2, Pongsakorn Buraphat1, Phuwanat Sakornsakolpat1, Kulthida Vaeteewoottacharn3, Seiji Okada4, Siwanon Jirawatnotai1, Somponnat Sampattavanich1.
Abstract
Cholangiocarcinoma (CCA) is rare cancer with the highest incidence in Eastern and Southeast Asian countries. Advanced CCA patients rely on chemotherapeutic regimens that offer unsatisfied clinical outcomes. We developed a comprehensive drug response profiling to investigate potential new drugs using CCA cell lines from Thai and Japanese patients against 100 approved anti-cancer drugs. We identified two major CCA subgroups that displayed unique molecular pathways from our integrative pan-omic and ligand-induced pathway activation analyses. MEK and Src inhibitors specifically killed the CCA1 subgroup without causing cytotoxicity to the normal cholangiocyte. Next, we developed the CCA45 signature to classify CCA patients based on their transcriptomic data. Our CCA45 signature could accurately predict prognosis, especially for Asian CCA patients. Our study provides a comprehensive public resource for drug repurposing in CCA and introduces analytical strategies for prioritizing cancer therapeutic agents for other rare cancer.Entities:
Keywords: Cancer; Cancer systems biology; Omics
Year: 2022 PMID: 36248745 PMCID: PMC9563539 DOI: 10.1016/j.isci.2022.105182
Source DB: PubMed Journal: iScience ISSN: 2589-0042