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The Prognostic and Predictive Value of SOX2(+) Cell Densities in Patients Treated for Colorectal Cancer

SOX2 (sex-determining region-Y homeobox-2) is a transcription factor essential for the maintenance of pluripotency and is also associated with stem-cell-like properties in preclinical cancer models. Our previous study on a cohort of stage III colon cancer patients demonstrated high SOX2(+) cell dens...

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Autores principales: Miller, Tim J., McCoy, Melanie J., Lee-Pullen, Tracey F., Anyaegbu, Chidozie C., Hemmings, Christine, Bulsara, Max K., Platell, Cameron F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7280991/
https://www.ncbi.nlm.nih.gov/pubmed/32365581
http://dx.doi.org/10.3390/cancers12051110
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author Miller, Tim J.
McCoy, Melanie J.
Lee-Pullen, Tracey F.
Anyaegbu, Chidozie C.
Hemmings, Christine
Bulsara, Max K.
Platell, Cameron F.
author_facet Miller, Tim J.
McCoy, Melanie J.
Lee-Pullen, Tracey F.
Anyaegbu, Chidozie C.
Hemmings, Christine
Bulsara, Max K.
Platell, Cameron F.
author_sort Miller, Tim J.
collection PubMed
description SOX2 (sex-determining region-Y homeobox-2) is a transcription factor essential for the maintenance of pluripotency and is also associated with stem-cell-like properties in preclinical cancer models. Our previous study on a cohort of stage III colon cancer patients demonstrated high SOX2(+) cell densities were associated with poor prognosis. However, most patients were treated with adjuvant chemotherapy so the prognostic value of SOX2 could not be assessed independently from its value as a predictive marker for non-response to chemotherapy. This study aimed to assess whether SOX2 was a true prognostic marker or a marker for chemotherapy response in a historical cohort of patients, a high proportion of whom were chemotherapy-naïve. SOX2 immunostaining was performed on tissue micro-arrays containing tumor cores from 797 patients with stage II and III colorectal cancer. SOX2(+) cell densities were then quantified with StrataQuest digital image analysis software. Overall survival was assessed using Kaplan–Meier estimates and Cox regression. It was found that high SOX2(+) cell densities were not associated with poor overall survival. Furthermore, all patients had a significant improvement in survival after 5-fluorouracil (5-FU) treatment, irrespective of their SOX2(+) cell density. Therefore, SOX2(+) cell densities were not associated with prognosis or chemotherapy benefit in this study. This is in contrast to our previous study, in which most patients received oxaliplatin as part of their treatment, in addition to 5-FU. This suggests SOX2 may predict response to oxaliplatin treatment, but not 5-FU.
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spelling pubmed-72809912020-06-15 The Prognostic and Predictive Value of SOX2(+) Cell Densities in Patients Treated for Colorectal Cancer Miller, Tim J. McCoy, Melanie J. Lee-Pullen, Tracey F. Anyaegbu, Chidozie C. Hemmings, Christine Bulsara, Max K. Platell, Cameron F. Cancers (Basel) Article SOX2 (sex-determining region-Y homeobox-2) is a transcription factor essential for the maintenance of pluripotency and is also associated with stem-cell-like properties in preclinical cancer models. Our previous study on a cohort of stage III colon cancer patients demonstrated high SOX2(+) cell densities were associated with poor prognosis. However, most patients were treated with adjuvant chemotherapy so the prognostic value of SOX2 could not be assessed independently from its value as a predictive marker for non-response to chemotherapy. This study aimed to assess whether SOX2 was a true prognostic marker or a marker for chemotherapy response in a historical cohort of patients, a high proportion of whom were chemotherapy-naïve. SOX2 immunostaining was performed on tissue micro-arrays containing tumor cores from 797 patients with stage II and III colorectal cancer. SOX2(+) cell densities were then quantified with StrataQuest digital image analysis software. Overall survival was assessed using Kaplan–Meier estimates and Cox regression. It was found that high SOX2(+) cell densities were not associated with poor overall survival. Furthermore, all patients had a significant improvement in survival after 5-fluorouracil (5-FU) treatment, irrespective of their SOX2(+) cell density. Therefore, SOX2(+) cell densities were not associated with prognosis or chemotherapy benefit in this study. This is in contrast to our previous study, in which most patients received oxaliplatin as part of their treatment, in addition to 5-FU. This suggests SOX2 may predict response to oxaliplatin treatment, but not 5-FU. MDPI 2020-04-29 /pmc/articles/PMC7280991/ /pubmed/32365581 http://dx.doi.org/10.3390/cancers12051110 Text en © 2020 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
Miller, Tim J.
McCoy, Melanie J.
Lee-Pullen, Tracey F.
Anyaegbu, Chidozie C.
Hemmings, Christine
Bulsara, Max K.
Platell, Cameron F.
The Prognostic and Predictive Value of SOX2(+) Cell Densities in Patients Treated for Colorectal Cancer
title The Prognostic and Predictive Value of SOX2(+) Cell Densities in Patients Treated for Colorectal Cancer
title_full The Prognostic and Predictive Value of SOX2(+) Cell Densities in Patients Treated for Colorectal Cancer
title_fullStr The Prognostic and Predictive Value of SOX2(+) Cell Densities in Patients Treated for Colorectal Cancer
title_full_unstemmed The Prognostic and Predictive Value of SOX2(+) Cell Densities in Patients Treated for Colorectal Cancer
title_short The Prognostic and Predictive Value of SOX2(+) Cell Densities in Patients Treated for Colorectal Cancer
title_sort prognostic and predictive value of sox2(+) cell densities in patients treated for colorectal cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7280991/
https://www.ncbi.nlm.nih.gov/pubmed/32365581
http://dx.doi.org/10.3390/cancers12051110
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