4.6 Article

Colorectal Cancer Classification and Survival Analysis Based on an Integrated RNA and DNA Molecular Signature

Journal

CURRENT BIOINFORMATICS
Volume 16, Issue 4, Pages 583-600

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1574893615999200711170445

Keywords

Colorectal cancer; FFPE; microarray; RAS pathway signatures; RNASeq; molecular

Funding

  1. GSK Africa NonCommunicable Disease Open Lab through the DELTAS Africa SubSaharan African Consortium for Advanced Biostatistics (SSACAB) [107754/Z/15]

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This study developed a hybrid (DNA mutation and RNA expression) signature to predict the mutation status and survival of CRC patients. The results showed that the signature had high accuracy, sensitivity, specificity, and AUC for mutation status, and was prognostic for survival in CRC patients. The study suggests potential clinical utility of the signature in CRC diagnosis and therapy.
Background: Colorectal cancer (CRC) is the third most common cancer among women and men in the USA, and recent studies have shown an increasing incidence in less developed regions, including Sub-Saharan Africa (SSA). We developed a hybrid (DNA mutation and RNA expression) signature and assessed its predictive properties for the mutation status and survival of CRC patients. Methods: Publicly-available microarray and RNASeq data from 54 matched formalin-fixed paraffin-embedded (FFPE) samples from the Affymetrix GeneChip and RNASeq platforms, were used to obtain differentially expressed genes between mutant and wild-type samples. We applied the support-vector machines, artificial neural networks, random forests, k-nearest neighbor, na & iuml;ve Bayes, negative binomial linear discriminant analysis, and the Poisson linear discriminant analysis algorithms for classification. Cox proportional hazards model was used for survival analysis. Results: Compared to the genelist from each of the individual platforms, the hybrid genelist had the highest accuracy, sensitivity, specificity, and AUC for mutation status, across all the classifiers and is prognostic for survival in patients with CRC. NBLDA method was the best performer on the RNASeq data, while the SVM method was the most suitable classifier for CRC across the two data types. Nine genes were found to be predictive of survival. Conclusion: This signature could be useful in clinical practice, especially for colorectal cancer diagnosis and therapy. Future studies should determine the effectiveness of integration in cancer survival analysis and the application on unbalanced data, where the classes are of different sizes, as well as on data with multiple classes.

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