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A comparison of 12-gene colon cancer assay gene expression in African American and Caucasian patients with stage II colon cancer

BACKGROUND: African American (AA) colon cancer patients have a worse prognosis than Caucasian (CA) colon cancer patients, however, reasons for this disparity are not well understood. To determine if tumor biology might contribute to differential prognosis, we measured recurrence risk and gene expres...

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Autores principales: Govindarajan, Rangaswamy, Posey, James, Chao, Calvin Y., Lu, Ruixiao, Jadhav, Trafina, Javed, Ahmed Y., Javed, Awais, Mahmoud, Fade A., Osarogiagbon, Raymond U., Manne, Upender
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4912774/
https://www.ncbi.nlm.nih.gov/pubmed/27316467
http://dx.doi.org/10.1186/s12885-016-2365-3
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author Govindarajan, Rangaswamy
Posey, James
Chao, Calvin Y.
Lu, Ruixiao
Jadhav, Trafina
Javed, Ahmed Y.
Javed, Awais
Mahmoud, Fade A.
Osarogiagbon, Raymond U.
Manne, Upender
author_facet Govindarajan, Rangaswamy
Posey, James
Chao, Calvin Y.
Lu, Ruixiao
Jadhav, Trafina
Javed, Ahmed Y.
Javed, Awais
Mahmoud, Fade A.
Osarogiagbon, Raymond U.
Manne, Upender
author_sort Govindarajan, Rangaswamy
collection PubMed
description BACKGROUND: African American (AA) colon cancer patients have a worse prognosis than Caucasian (CA) colon cancer patients, however, reasons for this disparity are not well understood. To determine if tumor biology might contribute to differential prognosis, we measured recurrence risk and gene expression using the Oncotype DX® Colon Cancer Assay (12-gene assay) and compared the Recurrence Score results and gene expression profiles between AA patients and CA patients with stage II colon cancer. METHODS: We retrieved demographic, clinical, and archived tumor tissues from stage II colon cancer patients at four institutions. The 12-gene assay and mismatch repair (MMR) status were performed by Genomic Health (Redwood City, California). Student’s t-test and the Wilcoxon rank sum test were used to compare Recurrence Score data and gene expression data from AA and CA patients (SAS Enterprise Guide 5.1). RESULTS: Samples from 122 AA and 122 CA patients were analyzed. There were 118 women (63 AA, 55 CA) and 126 men (59 AA, 67 CA). Median age was 66 years for AA patients and 68 for CA patients. Age, gender, year of surgery, pathologic T-stage, tumor location, the number of lymph nodes examined, lymphovascular invasion, and MMR status were not significantly different between groups (p = 0.93). The mean Recurrence Score result for AA patients (27.9 ± 12.8) and CA patients (28.1 ± 11.8) was not significantly different and the proportions of patients with high Recurrence Score values (≥41) were similar between the groups (17/122 AA; 15/122 CA). None of the gene expression variables, either single genes or gene groups (cell cycle group, stromal group, BGN1, FAP, INHBA1, Ki67, MYBL2, cMYC and GADD45B), was significantly different between the racial groups. After controlling for clinical and pathologic covariates, the means and distributions of Recurrence Score results and gene expression profiles showed no statistically significant difference between patient groups. CONCLUSION: The distribution of Recurrence Score results and gene expression data was similar in a cohort of AA and CA patients with stage II colon cancer and similar clinical characteristics, suggesting that tumor biology, as represented by the 12-gene assay, did not differ between patient groups.
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spelling pubmed-49127742016-06-19 A comparison of 12-gene colon cancer assay gene expression in African American and Caucasian patients with stage II colon cancer Govindarajan, Rangaswamy Posey, James Chao, Calvin Y. Lu, Ruixiao Jadhav, Trafina Javed, Ahmed Y. Javed, Awais Mahmoud, Fade A. Osarogiagbon, Raymond U. Manne, Upender BMC Cancer Research Article BACKGROUND: African American (AA) colon cancer patients have a worse prognosis than Caucasian (CA) colon cancer patients, however, reasons for this disparity are not well understood. To determine if tumor biology might contribute to differential prognosis, we measured recurrence risk and gene expression using the Oncotype DX® Colon Cancer Assay (12-gene assay) and compared the Recurrence Score results and gene expression profiles between AA patients and CA patients with stage II colon cancer. METHODS: We retrieved demographic, clinical, and archived tumor tissues from stage II colon cancer patients at four institutions. The 12-gene assay and mismatch repair (MMR) status were performed by Genomic Health (Redwood City, California). Student’s t-test and the Wilcoxon rank sum test were used to compare Recurrence Score data and gene expression data from AA and CA patients (SAS Enterprise Guide 5.1). RESULTS: Samples from 122 AA and 122 CA patients were analyzed. There were 118 women (63 AA, 55 CA) and 126 men (59 AA, 67 CA). Median age was 66 years for AA patients and 68 for CA patients. Age, gender, year of surgery, pathologic T-stage, tumor location, the number of lymph nodes examined, lymphovascular invasion, and MMR status were not significantly different between groups (p = 0.93). The mean Recurrence Score result for AA patients (27.9 ± 12.8) and CA patients (28.1 ± 11.8) was not significantly different and the proportions of patients with high Recurrence Score values (≥41) were similar between the groups (17/122 AA; 15/122 CA). None of the gene expression variables, either single genes or gene groups (cell cycle group, stromal group, BGN1, FAP, INHBA1, Ki67, MYBL2, cMYC and GADD45B), was significantly different between the racial groups. After controlling for clinical and pathologic covariates, the means and distributions of Recurrence Score results and gene expression profiles showed no statistically significant difference between patient groups. CONCLUSION: The distribution of Recurrence Score results and gene expression data was similar in a cohort of AA and CA patients with stage II colon cancer and similar clinical characteristics, suggesting that tumor biology, as represented by the 12-gene assay, did not differ between patient groups. BioMed Central 2016-06-18 /pmc/articles/PMC4912774/ /pubmed/27316467 http://dx.doi.org/10.1186/s12885-016-2365-3 Text en © Govindarajan et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Govindarajan, Rangaswamy
Posey, James
Chao, Calvin Y.
Lu, Ruixiao
Jadhav, Trafina
Javed, Ahmed Y.
Javed, Awais
Mahmoud, Fade A.
Osarogiagbon, Raymond U.
Manne, Upender
A comparison of 12-gene colon cancer assay gene expression in African American and Caucasian patients with stage II colon cancer
title A comparison of 12-gene colon cancer assay gene expression in African American and Caucasian patients with stage II colon cancer
title_full A comparison of 12-gene colon cancer assay gene expression in African American and Caucasian patients with stage II colon cancer
title_fullStr A comparison of 12-gene colon cancer assay gene expression in African American and Caucasian patients with stage II colon cancer
title_full_unstemmed A comparison of 12-gene colon cancer assay gene expression in African American and Caucasian patients with stage II colon cancer
title_short A comparison of 12-gene colon cancer assay gene expression in African American and Caucasian patients with stage II colon cancer
title_sort comparison of 12-gene colon cancer assay gene expression in african american and caucasian patients with stage ii colon cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4912774/
https://www.ncbi.nlm.nih.gov/pubmed/27316467
http://dx.doi.org/10.1186/s12885-016-2365-3
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