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Identification and Clinical Validation of a Novel 4 Gene-Signature with Prognostic Utility in Colorectal Cancer

Colorectal cancer (CRC) is a high burden disease with several genes involved in tumor progression. The aim of the present study was to identify, generate and clinically validate a novel gene signature to improve prediction of overall survival (OS) to effectively manage colorectal cancer. We explored...

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Autores principales: Ahluwalia, Pankaj, Mondal, Ashis K., Bloomer, Chance, Fulzele, Sadanand, Jones, Kimya, Ananth, Sudha, Gahlay, Gagandeep K., Heneidi, Saleh, Rojiani, Amyn M., Kota, Vamsi, Kolhe, Ravindra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6696416/
https://www.ncbi.nlm.nih.gov/pubmed/31387239
http://dx.doi.org/10.3390/ijms20153818
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author Ahluwalia, Pankaj
Mondal, Ashis K.
Bloomer, Chance
Fulzele, Sadanand
Jones, Kimya
Ananth, Sudha
Gahlay, Gagandeep K.
Heneidi, Saleh
Rojiani, Amyn M.
Kota, Vamsi
Kolhe, Ravindra
author_facet Ahluwalia, Pankaj
Mondal, Ashis K.
Bloomer, Chance
Fulzele, Sadanand
Jones, Kimya
Ananth, Sudha
Gahlay, Gagandeep K.
Heneidi, Saleh
Rojiani, Amyn M.
Kota, Vamsi
Kolhe, Ravindra
author_sort Ahluwalia, Pankaj
collection PubMed
description Colorectal cancer (CRC) is a high burden disease with several genes involved in tumor progression. The aim of the present study was to identify, generate and clinically validate a novel gene signature to improve prediction of overall survival (OS) to effectively manage colorectal cancer. We explored The Cancer Genome Atlas (TCGA), COAD and READ datasets (597 samples) from The Protein Atlas (TPA) database to extract a total of 595 candidate genes. In parallel, we identified 29 genes with perturbations in > 6 cancers which are also affected in CRC. These genes were entered in cBioportal to generate a 17 gene panel with highest perturbations. For clinical validation, this gene panel was tested on the FFPE tissues of colorectal cancer patients (88 patients) using Nanostring analysis. Using multivariate analysis, a high prognostic score (composite 4 gene signature—DPP7/2, YWHAB, MCM4 and FBXO46) was found to be a significant predictor of poor prognosis in CRC patients (HR: 3.42, 95% CI: 1.71–7.94, p < 0.001 *) along with stage (HR: 4.56, 95% CI: 1.35–19.15, p = 0.01 *). The Kaplan-Meier analysis also segregated patients on the basis of prognostic score (log-rank test, p = 0.001 *). The external validation using GEO dataset (GSE38832, 122 patients) corroborated the prognostic score (HR: 2.7, 95% CI: 1.99–3.73, p < 0.001 *). Additionally, higher score was able to differentiate stage II and III patients (130 patients) on the basis of OS (HR: 2.5, 95% CI: 1.78–3.63, p < 0.001 *). Overall, our results identify a novel 4 gene prognostic signature that has clinical utility in colorectal cancer.
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spelling pubmed-66964162019-09-05 Identification and Clinical Validation of a Novel 4 Gene-Signature with Prognostic Utility in Colorectal Cancer Ahluwalia, Pankaj Mondal, Ashis K. Bloomer, Chance Fulzele, Sadanand Jones, Kimya Ananth, Sudha Gahlay, Gagandeep K. Heneidi, Saleh Rojiani, Amyn M. Kota, Vamsi Kolhe, Ravindra Int J Mol Sci Article Colorectal cancer (CRC) is a high burden disease with several genes involved in tumor progression. The aim of the present study was to identify, generate and clinically validate a novel gene signature to improve prediction of overall survival (OS) to effectively manage colorectal cancer. We explored The Cancer Genome Atlas (TCGA), COAD and READ datasets (597 samples) from The Protein Atlas (TPA) database to extract a total of 595 candidate genes. In parallel, we identified 29 genes with perturbations in > 6 cancers which are also affected in CRC. These genes were entered in cBioportal to generate a 17 gene panel with highest perturbations. For clinical validation, this gene panel was tested on the FFPE tissues of colorectal cancer patients (88 patients) using Nanostring analysis. Using multivariate analysis, a high prognostic score (composite 4 gene signature—DPP7/2, YWHAB, MCM4 and FBXO46) was found to be a significant predictor of poor prognosis in CRC patients (HR: 3.42, 95% CI: 1.71–7.94, p < 0.001 *) along with stage (HR: 4.56, 95% CI: 1.35–19.15, p = 0.01 *). The Kaplan-Meier analysis also segregated patients on the basis of prognostic score (log-rank test, p = 0.001 *). The external validation using GEO dataset (GSE38832, 122 patients) corroborated the prognostic score (HR: 2.7, 95% CI: 1.99–3.73, p < 0.001 *). Additionally, higher score was able to differentiate stage II and III patients (130 patients) on the basis of OS (HR: 2.5, 95% CI: 1.78–3.63, p < 0.001 *). Overall, our results identify a novel 4 gene prognostic signature that has clinical utility in colorectal cancer. MDPI 2019-08-05 /pmc/articles/PMC6696416/ /pubmed/31387239 http://dx.doi.org/10.3390/ijms20153818 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ahluwalia, Pankaj
Mondal, Ashis K.
Bloomer, Chance
Fulzele, Sadanand
Jones, Kimya
Ananth, Sudha
Gahlay, Gagandeep K.
Heneidi, Saleh
Rojiani, Amyn M.
Kota, Vamsi
Kolhe, Ravindra
Identification and Clinical Validation of a Novel 4 Gene-Signature with Prognostic Utility in Colorectal Cancer
title Identification and Clinical Validation of a Novel 4 Gene-Signature with Prognostic Utility in Colorectal Cancer
title_full Identification and Clinical Validation of a Novel 4 Gene-Signature with Prognostic Utility in Colorectal Cancer
title_fullStr Identification and Clinical Validation of a Novel 4 Gene-Signature with Prognostic Utility in Colorectal Cancer
title_full_unstemmed Identification and Clinical Validation of a Novel 4 Gene-Signature with Prognostic Utility in Colorectal Cancer
title_short Identification and Clinical Validation of a Novel 4 Gene-Signature with Prognostic Utility in Colorectal Cancer
title_sort identification and clinical validation of a novel 4 gene-signature with prognostic utility in colorectal cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6696416/
https://www.ncbi.nlm.nih.gov/pubmed/31387239
http://dx.doi.org/10.3390/ijms20153818
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