4.7 Article

cSurvival: a web resource for biomarker interactions in cancer outcomes and in cell lines

期刊

BRIEFINGS IN BIOINFORMATICS
卷 23, 期 3, 页码 -

出版社

OXFORD UNIV PRESS
DOI: 10.1093/bib/bbac090

关键词

genetic interaction; survival analysis; TCGA; TARGET; DepMap; biomarker

资金

  1. Canadian Institutes of Health Research (CIHR) [PJT-153199]
  2. Natural Sciences and Engineering Research Council of Canada (NSERC) [RGPIN-2018-05133, RGPIN-2017-04722]
  3. Canada Research Chair [950231363]
  4. British Columbia Children's Hospital Research Institute Investigator Grant Award Program award
  5. Canada Research Chairs program

向作者/读者索取更多资源

Survival analysis is a valuable technique in cancer research for identifying prognostic biomarkers and genetic vulnerabilities. cSurvival is a newly developed analytical tool that allows for gene- and GS-level survival analysis, as well as integration of clinical and experimental data, showing great potential for applications in cancer studies.
Survival analysis is a technique for identifying prognostic biomarkers and genetic vulnerabilities in cancer studies. Large-scale consortium-based projects have profiled >11 000 adult and >4000 pediatric tumor cases with clinical outcomes and multiomics approaches. This provides a resource for investigating molecular-level cancer etiologies using clinical correlations. Although cancers often arise from multiple genetic vulnerabilities and have deregulated gene sets (GSs), existing survival analysis protocols can report only on individual genes. Additionally, there is no systematic method to connect clinical outcomes with experimental (cell line) data. To address these gaps, we developed cSurvival (https://tau.cmmt.ubc.ca/cSurvival). cSurvival provides a user-adjustable analytical pipeline with a curated, integrated database and offers three main advances: (i) joint analysis with two genomic predictors to identify interacting biomarkers, including new algorithms to identify optimal cutoffs for two continuous predictors; (ii) survival analysis not only at the gene, but also the GS level; and (iii) integration of clinical and experimental cell line studies to generate synergistic biological insights. To demonstrate these advances, we report three case studies. We confirmed findings of autophagy-dependent survival in colorectal cancers and of synergistic negative effects between high expression of SLC7A11 and SLC2A1 on outcomes in several cancers. We further used cSurvival to identify high expression of the Nrf2-antioxidant response element pathway as a main indicator for lung cancer prognosis and for cellular resistance to oxidative stress-inducing drugs. Altogether, these analyses demonstrate cSurvival's ability to support biomarker prognosis and interaction analysis via gene- and GS-level approaches and to integrate clinical and experimental biomedical studies.

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