EMAST is associated with a poor prognosis in microsatellite instable metastatic colorectal cancer.

<h4>Purpose</h4>To determine the frequency and prognostic value of elevated microsatellite alterations at selected tetranucleotide repeats (EMAST) in metastatic colorectal cancer (mCRC) patients in relation to microsatellite instability (MSI) status and MSH3 protein expression.<h4>...

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Main Authors: Sabine Venderbosch, Shannon van Lent-van Vliet, Anton F J de Haan, Marjolijn J Ligtenberg, Monique Goossens, Cornelis J A Punt, Miriam Koopman, Iris D Nagtegaal
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0124538
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spelling doaj-73113240e7d94246b0ef74adc0fbc31f2021-03-04T08:18:50ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01104e012453810.1371/journal.pone.0124538EMAST is associated with a poor prognosis in microsatellite instable metastatic colorectal cancer.Sabine VenderboschShannon van Lent-van VlietAnton F J de HaanMarjolijn J LigtenbergMonique GoossensCornelis J A PuntMiriam KoopmanIris D Nagtegaal<h4>Purpose</h4>To determine the frequency and prognostic value of elevated microsatellite alterations at selected tetranucleotide repeats (EMAST) in metastatic colorectal cancer (mCRC) patients in relation to microsatellite instability (MSI) status and MSH3 protein expression.<h4>Material and methods</h4>The frequency of EMAST was evaluated in mCRC patients with MSI tumors and microsatellite stable (MSS) tumors. A literature overview was performed to compare the frequency of EMAST in our study with existing data. Immunohistochemistry for MSH3 was compared with EMAST status. Outcome was studied in terms of overall survival (OS) of mCRC patients with MSI and MSS tumors.<h4>Results</h4>EMAST was evaluated in 89 patients with MSI tumors (including 39 patients with Lynch syndrome) and 94 patients with MSS tumors. EMAST was observed in 45.9% (84 out of 183) of patients, with an increased frequency in MSI tumors (79.8% versus 13.8%, p < 0.001). We found no correlation between EMAST and MSH3 protein expression. There was no effect of EMAST on prognosis in patients with MSS tumors, but patients with MSI / non-EMAST tumors had a significantly better prognosis than patients with MSI / EMAST tumors (OS: HR 3.22, 95% CI 1.25-8.30).<h4>Conclusion</h4>Frequency of EMAST was increased in mCRC patients with MSI tumors, compared to MSS tumors. Our data suggest that the presence of EMAST correlates with worse OS in these patients. There was no effect of EMAST on the prognosis of patients with MSS tumors. A limitation of our study is the small number of patients in our subgroup analysis.https://doi.org/10.1371/journal.pone.0124538
collection DOAJ
language English
format Article
sources DOAJ
author Sabine Venderbosch
Shannon van Lent-van Vliet
Anton F J de Haan
Marjolijn J Ligtenberg
Monique Goossens
Cornelis J A Punt
Miriam Koopman
Iris D Nagtegaal
spellingShingle Sabine Venderbosch
Shannon van Lent-van Vliet
Anton F J de Haan
Marjolijn J Ligtenberg
Monique Goossens
Cornelis J A Punt
Miriam Koopman
Iris D Nagtegaal
EMAST is associated with a poor prognosis in microsatellite instable metastatic colorectal cancer.
PLoS ONE
author_facet Sabine Venderbosch
Shannon van Lent-van Vliet
Anton F J de Haan
Marjolijn J Ligtenberg
Monique Goossens
Cornelis J A Punt
Miriam Koopman
Iris D Nagtegaal
author_sort Sabine Venderbosch
title EMAST is associated with a poor prognosis in microsatellite instable metastatic colorectal cancer.
title_short EMAST is associated with a poor prognosis in microsatellite instable metastatic colorectal cancer.
title_full EMAST is associated with a poor prognosis in microsatellite instable metastatic colorectal cancer.
title_fullStr EMAST is associated with a poor prognosis in microsatellite instable metastatic colorectal cancer.
title_full_unstemmed EMAST is associated with a poor prognosis in microsatellite instable metastatic colorectal cancer.
title_sort emast is associated with a poor prognosis in microsatellite instable metastatic colorectal cancer.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description <h4>Purpose</h4>To determine the frequency and prognostic value of elevated microsatellite alterations at selected tetranucleotide repeats (EMAST) in metastatic colorectal cancer (mCRC) patients in relation to microsatellite instability (MSI) status and MSH3 protein expression.<h4>Material and methods</h4>The frequency of EMAST was evaluated in mCRC patients with MSI tumors and microsatellite stable (MSS) tumors. A literature overview was performed to compare the frequency of EMAST in our study with existing data. Immunohistochemistry for MSH3 was compared with EMAST status. Outcome was studied in terms of overall survival (OS) of mCRC patients with MSI and MSS tumors.<h4>Results</h4>EMAST was evaluated in 89 patients with MSI tumors (including 39 patients with Lynch syndrome) and 94 patients with MSS tumors. EMAST was observed in 45.9% (84 out of 183) of patients, with an increased frequency in MSI tumors (79.8% versus 13.8%, p < 0.001). We found no correlation between EMAST and MSH3 protein expression. There was no effect of EMAST on prognosis in patients with MSS tumors, but patients with MSI / non-EMAST tumors had a significantly better prognosis than patients with MSI / EMAST tumors (OS: HR 3.22, 95% CI 1.25-8.30).<h4>Conclusion</h4>Frequency of EMAST was increased in mCRC patients with MSI tumors, compared to MSS tumors. Our data suggest that the presence of EMAST correlates with worse OS in these patients. There was no effect of EMAST on the prognosis of patients with MSS tumors. A limitation of our study is the small number of patients in our subgroup analysis.
url https://doi.org/10.1371/journal.pone.0124538
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