Literature DB >> 25236463

Translating bioinformatics in oncology: guilt-by-profiling analysis and identification of KIF18B and CDCA3 as novel driver genes in carcinogenesis.

Timo Itzel1, Peter Scholz1, Thorsten Maass1, Markus Krupp1, Jens U Marquardt1, Susanne Strand1, Diana Becker1, Frank Staib1, Harald Binder1, Stephanie Roessler1, Xin Wei Wang1, Snorri Thorgeirsson1, Martina Müller1, Peter R Galle1, Andreas Teufel1.   

Abstract

MOTIVATION: Co-regulated genes are not identified in traditional microarray analyses, but may theoretically be closely functionally linked [guilt-by-association (GBA), guilt-by-profiling]. Thus, bioinformatics procedures for guilt-by-profiling/association analysis have yet to be applied to large-scale cancer biology. We analyzed 2158 full cancer transcriptomes from 163 diverse cancer entities in regard of their similarity of gene expression, using Pearson's correlation coefficient (CC). Subsequently, 428 highly co-regulated genes (|CC| ≥ 0.8) were clustered unsupervised to obtain small co-regulated networks. A major subnetwork containing 61 closely co-regulated genes showed highly significant enrichment of cancer bio-functions. All genes except kinesin family member 18B (KIF18B) and cell division cycle associated 3 (CDCA3) were of confirmed relevance for tumor biology. Therefore, we independently analyzed their differential regulation in multiple tumors and found severe deregulation in liver, breast, lung, ovarian and kidney cancers, thus proving our GBA hypothesis. Overexpression of KIF18B and CDCA3 in hepatoma cells and subsequent microarray analysis revealed significant deregulation of central cell cycle regulatory genes. Consistently, RT-PCR and proliferation assay confirmed the role of both genes in cell cycle progression. Finally, the prognostic significance of the identified KIF18B- and CDCA3-dependent predictors (P = 0.01, P = 0.04) was demonstrated in three independent HCC cohorts and several other tumors. In summary, we proved the efficacy of large-scale guilt-by-profiling/association strategies in oncology. We identified two novel oncogenes and functionally characterized them. The strong prognostic importance of downstream predictors for HCC and many other tumors indicates the clinical relevance of our findings. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
© The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

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Year:  2014        PMID: 25236463      PMCID: PMC4287940          DOI: 10.1093/bioinformatics/btu586

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  39 in total

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5.  Cluster analysis and display of genome-wide expression patterns.

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Journal:  Genome Biol       Date:  2008-06-27       Impact factor: 13.583

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  26 in total

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Review 3.  Kinesin superfamily: roles in breast cancer, patient prognosis and therapeutics.

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6.  Distinct expression of CDCA3, CDCA5, and CDCA8 leads to shorter relapse free survival in breast cancer patient.

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7.  Tumor-infiltrating B cells producing antitumor active immunoglobulins in resected HCC prolong patient survival.

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8.  Silymarin-mediated regulation of the cell cycle and DNA damage response exerts antitumor activity in human hepatocellular carcinoma.

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9.  KIF18B promotes tumor progression through activating the Wnt/β-catenin pathway in cervical cancer.

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Journal:  Onco Targets Ther       Date:  2018-03-28       Impact factor: 4.147

10.  Coexpression Network Analysis of Genes Related to the Characteristics of Tumor Stemness in Triple-Negative Breast Cancer.

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