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RCC1 Expression as a Prognostic Marker in Colorectal Liver Oligometastases
Introduction: Regulator of chromatin condensation 1 (RCC1) is a major guanine-nucleotide exchange factor for Ran GTPase, and it plays key roles in various biological processes. Previous studies have found that RCC1 may play a role in the development of tumors, but little is known about the relations...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8674189/ https://www.ncbi.nlm.nih.gov/pubmed/34924821 http://dx.doi.org/10.3389/pore.2021.1610077 |
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author | Deng, Yuxiang Yu, Long Zhao, Yujie Peng, Jianhong Xu, Yanbo Qin, JiaYi Xiao, Binyi Liu, Songran Li, Mei Fang, Yujing Pan, Zhizhong |
author_facet | Deng, Yuxiang Yu, Long Zhao, Yujie Peng, Jianhong Xu, Yanbo Qin, JiaYi Xiao, Binyi Liu, Songran Li, Mei Fang, Yujing Pan, Zhizhong |
author_sort | Deng, Yuxiang |
collection | PubMed |
description | Introduction: Regulator of chromatin condensation 1 (RCC1) is a major guanine-nucleotide exchange factor for Ran GTPase, and it plays key roles in various biological processes. Previous studies have found that RCC1 may play a role in the development of tumors, but little is known about the relationship between RCC1 and colorectal liver oligometastases (CLOs). Methods: One hundred and twenty-nine pairs of matched human CLO samples, including both primary tumor and its liver metastasis specimens, were subjected to immunohistochemistry to determine the location and expression levels of RCC1. Associations between RCC1 and survival as well as gene expression profiling were explored. Results: In this study, we first observed that RCC1 was mildly increased in CLO tumor tissues compared with normal tissues, and the localization was primarily nuclear. In addition, our study found that high RCC1 expression in liver oligometastases was an independent prognostic marker for unfavorable recurrence-free survival and overall survival (p = 0.036 and p = 0.016). Gene expression profiles generated from microarray analysis showed that RCC1 was involved in pathways including “Myc targets,” “E2F targets” and “DNA repair” pathways. Conclusion: Our data indicated that RCC1 was expressed mainly in the nucleus, and strong and significant associations were found between RCC1 expression levels and the survival of CLO patients. These findings indicated that RCC1 may play a role in CLO development. |
format | Online Article Text |
id | pubmed-8674189 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86741892021-12-17 RCC1 Expression as a Prognostic Marker in Colorectal Liver Oligometastases Deng, Yuxiang Yu, Long Zhao, Yujie Peng, Jianhong Xu, Yanbo Qin, JiaYi Xiao, Binyi Liu, Songran Li, Mei Fang, Yujing Pan, Zhizhong Pathol Oncol Res Pathology and Oncology Archive Introduction: Regulator of chromatin condensation 1 (RCC1) is a major guanine-nucleotide exchange factor for Ran GTPase, and it plays key roles in various biological processes. Previous studies have found that RCC1 may play a role in the development of tumors, but little is known about the relationship between RCC1 and colorectal liver oligometastases (CLOs). Methods: One hundred and twenty-nine pairs of matched human CLO samples, including both primary tumor and its liver metastasis specimens, were subjected to immunohistochemistry to determine the location and expression levels of RCC1. Associations between RCC1 and survival as well as gene expression profiling were explored. Results: In this study, we first observed that RCC1 was mildly increased in CLO tumor tissues compared with normal tissues, and the localization was primarily nuclear. In addition, our study found that high RCC1 expression in liver oligometastases was an independent prognostic marker for unfavorable recurrence-free survival and overall survival (p = 0.036 and p = 0.016). Gene expression profiles generated from microarray analysis showed that RCC1 was involved in pathways including “Myc targets,” “E2F targets” and “DNA repair” pathways. Conclusion: Our data indicated that RCC1 was expressed mainly in the nucleus, and strong and significant associations were found between RCC1 expression levels and the survival of CLO patients. These findings indicated that RCC1 may play a role in CLO development. Frontiers Media S.A. 2021-12-02 /pmc/articles/PMC8674189/ /pubmed/34924821 http://dx.doi.org/10.3389/pore.2021.1610077 Text en Copyright © 2021 Deng, Yu, Zhao, Peng, Xu, Qin, Xiao, Liu, Li, Fang and Pan. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pathology and Oncology Archive Deng, Yuxiang Yu, Long Zhao, Yujie Peng, Jianhong Xu, Yanbo Qin, JiaYi Xiao, Binyi Liu, Songran Li, Mei Fang, Yujing Pan, Zhizhong RCC1 Expression as a Prognostic Marker in Colorectal Liver Oligometastases |
title | RCC1 Expression as a Prognostic Marker in Colorectal Liver Oligometastases |
title_full | RCC1 Expression as a Prognostic Marker in Colorectal Liver Oligometastases |
title_fullStr | RCC1 Expression as a Prognostic Marker in Colorectal Liver Oligometastases |
title_full_unstemmed | RCC1 Expression as a Prognostic Marker in Colorectal Liver Oligometastases |
title_short | RCC1 Expression as a Prognostic Marker in Colorectal Liver Oligometastases |
title_sort | rcc1 expression as a prognostic marker in colorectal liver oligometastases |
topic | Pathology and Oncology Archive |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8674189/ https://www.ncbi.nlm.nih.gov/pubmed/34924821 http://dx.doi.org/10.3389/pore.2021.1610077 |
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