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Clinical Implications of Microsatellite Instability in T1 Colorectal Cancer

PURPOSE: The estimation of regional lymph node metastasis (LNM) risk in T1 colorectal cancer is based on histologic examination and imaging of the primary tumor. High-frequency microsatellite instability (MSI-H) is likely to decrease the possibility of metastasis to either regional lymph nodes or di...

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Autores principales: Kang, Jeonghyun, Lee, Hak Woo, Kim, Im-kyung, Kim, Nam Kyu, Sohn, Seung-Kook, Lee, Kang Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Yonsei University College of Medicine 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4276753/
https://www.ncbi.nlm.nih.gov/pubmed/25510762
http://dx.doi.org/10.3349/ymj.2015.56.1.175
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author Kang, Jeonghyun
Lee, Hak Woo
Kim, Im-kyung
Kim, Nam Kyu
Sohn, Seung-Kook
Lee, Kang Young
author_facet Kang, Jeonghyun
Lee, Hak Woo
Kim, Im-kyung
Kim, Nam Kyu
Sohn, Seung-Kook
Lee, Kang Young
author_sort Kang, Jeonghyun
collection PubMed
description PURPOSE: The estimation of regional lymph node metastasis (LNM) risk in T1 colorectal cancer is based on histologic examination and imaging of the primary tumor. High-frequency microsatellite instability (MSI-H) is likely to decrease the possibility of metastasis to either regional lymph nodes or distant organs in colorectal cancers. This study evaluated the clinical implications of MSI in T1 colorectal cancer with emphasis on the usefulness of MSI as a predictive factor for regional LNM. MATERIALS AND METHODS: A total of 133 patients who underwent radical resection for T1 colorectal cancer were included. Genomic DNA was extracted from normal and tumor tissues and amplified by polymerase chain reaction (PCR). Five microsatellite markers, BAT-25, BAT-26, D2S123, D5S346, and D17S250, were used. MSI and clinicopathological parameters were evaluated as potential predictors of LNM using univariate and multivariate analyses. RESULTS: Among 133 T1 colorectal cancer patients, MSI-H, low-frequency microsatellite instability (MSI-L), and microsatellite stable (MSS) colorectal cancers accounted for 7.5%, 6%, and 86.5%, respectively. MSI-H tumors showed a female predominance, a proximal location and more retrieved lymph nodes. Twenty-two patients (16.5%) had regional LNM. Lymphovascular invasion and depth of invasion were significantly associated with LNM. There was no LNM in 10 MSI-H patients; however, MSI status was not significantly correlated with LNM. Disease-free survival did not differ between patients with MSI-H and those with MSI-L/MSS. CONCLUSION: MSI status could serve as a negative predictive factor in estimating LNM in T1 colorectal cancer, given that LNM was not detected in MSI-H patients. However, validation of our result in a different cohort is necessary.
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spelling pubmed-42767532015-01-01 Clinical Implications of Microsatellite Instability in T1 Colorectal Cancer Kang, Jeonghyun Lee, Hak Woo Kim, Im-kyung Kim, Nam Kyu Sohn, Seung-Kook Lee, Kang Young Yonsei Med J Original Article PURPOSE: The estimation of regional lymph node metastasis (LNM) risk in T1 colorectal cancer is based on histologic examination and imaging of the primary tumor. High-frequency microsatellite instability (MSI-H) is likely to decrease the possibility of metastasis to either regional lymph nodes or distant organs in colorectal cancers. This study evaluated the clinical implications of MSI in T1 colorectal cancer with emphasis on the usefulness of MSI as a predictive factor for regional LNM. MATERIALS AND METHODS: A total of 133 patients who underwent radical resection for T1 colorectal cancer were included. Genomic DNA was extracted from normal and tumor tissues and amplified by polymerase chain reaction (PCR). Five microsatellite markers, BAT-25, BAT-26, D2S123, D5S346, and D17S250, were used. MSI and clinicopathological parameters were evaluated as potential predictors of LNM using univariate and multivariate analyses. RESULTS: Among 133 T1 colorectal cancer patients, MSI-H, low-frequency microsatellite instability (MSI-L), and microsatellite stable (MSS) colorectal cancers accounted for 7.5%, 6%, and 86.5%, respectively. MSI-H tumors showed a female predominance, a proximal location and more retrieved lymph nodes. Twenty-two patients (16.5%) had regional LNM. Lymphovascular invasion and depth of invasion were significantly associated with LNM. There was no LNM in 10 MSI-H patients; however, MSI status was not significantly correlated with LNM. Disease-free survival did not differ between patients with MSI-H and those with MSI-L/MSS. CONCLUSION: MSI status could serve as a negative predictive factor in estimating LNM in T1 colorectal cancer, given that LNM was not detected in MSI-H patients. However, validation of our result in a different cohort is necessary. Yonsei University College of Medicine 2015-01-01 2014-12-10 /pmc/articles/PMC4276753/ /pubmed/25510762 http://dx.doi.org/10.3349/ymj.2015.56.1.175 Text en © Copyright: Yonsei University College of Medicine 2015 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kang, Jeonghyun
Lee, Hak Woo
Kim, Im-kyung
Kim, Nam Kyu
Sohn, Seung-Kook
Lee, Kang Young
Clinical Implications of Microsatellite Instability in T1 Colorectal Cancer
title Clinical Implications of Microsatellite Instability in T1 Colorectal Cancer
title_full Clinical Implications of Microsatellite Instability in T1 Colorectal Cancer
title_fullStr Clinical Implications of Microsatellite Instability in T1 Colorectal Cancer
title_full_unstemmed Clinical Implications of Microsatellite Instability in T1 Colorectal Cancer
title_short Clinical Implications of Microsatellite Instability in T1 Colorectal Cancer
title_sort clinical implications of microsatellite instability in t1 colorectal cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4276753/
https://www.ncbi.nlm.nih.gov/pubmed/25510762
http://dx.doi.org/10.3349/ymj.2015.56.1.175
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