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RRBP1 overexpression is associated with progression and prognosis in endometrial endometrioid adenocarcinoma
BACKGROUND: Currently, ribosome-binding protein 1 (RRBP1) is considered to be a novel oncogene that is overexpressed in colorectal cancer, lung cancer, mammary cancer, esophageal cancer and other carcinomas. However, the relationship between RRBP1 and endometrioid-type endometrial carcinoma (EC) rem...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6347782/ https://www.ncbi.nlm.nih.gov/pubmed/30684972 http://dx.doi.org/10.1186/s13000-019-0784-6 |
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author | Liu, Shuang Lin, Mu Ji, Hongying Ding, Jing Zhu, Jiaqi Ma, Rong Meng, Fanling |
author_facet | Liu, Shuang Lin, Mu Ji, Hongying Ding, Jing Zhu, Jiaqi Ma, Rong Meng, Fanling |
author_sort | Liu, Shuang |
collection | PubMed |
description | BACKGROUND: Currently, ribosome-binding protein 1 (RRBP1) is considered to be a novel oncogene that is overexpressed in colorectal cancer, lung cancer, mammary cancer, esophageal cancer and other carcinomas. However, the relationship between RRBP1 and endometrioid-type endometrial carcinoma (EC) remains unknown. Our purpose is to explore the function of RRBP1 in endometrioid-type endometrial carcinoma. METHODS: We investigated the expression of RRBP1 protein by immunohistochemistry on paraffin-embedded surgical specimens from one hundred thirty patients with endometrioid-type endometrial carcinoma. We also evaluated the differences in RRBP1 expression between endometrial cancer samples (n = 35) and normal endometrial tissues (n = 19) by western blotting. RESULTS: RRBP1 was more highly expressed in endometrial cancer samples than in normal samples (P < 0.05). High levels of expression of RRBP1 were strongly correlated with pathological features, such as the Federation of Gynecology and Obstetrics (FIGO) stage, histological grade, depth of myometrial invasion and lymph node metastasis (P < 0.05). Furthermore, RRBP1 expression was an independent prognostic factor for overall survival (OS) and disease-free survival (DFS) in patients with EC (both P < 0.05). CONCLUSION: This experiment identifies the utility of RRBP1 in predicting EC prognosis, revealing that it may be a potential target for therapeutics of EC. |
format | Online Article Text |
id | pubmed-6347782 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63477822019-01-30 RRBP1 overexpression is associated with progression and prognosis in endometrial endometrioid adenocarcinoma Liu, Shuang Lin, Mu Ji, Hongying Ding, Jing Zhu, Jiaqi Ma, Rong Meng, Fanling Diagn Pathol Research BACKGROUND: Currently, ribosome-binding protein 1 (RRBP1) is considered to be a novel oncogene that is overexpressed in colorectal cancer, lung cancer, mammary cancer, esophageal cancer and other carcinomas. However, the relationship between RRBP1 and endometrioid-type endometrial carcinoma (EC) remains unknown. Our purpose is to explore the function of RRBP1 in endometrioid-type endometrial carcinoma. METHODS: We investigated the expression of RRBP1 protein by immunohistochemistry on paraffin-embedded surgical specimens from one hundred thirty patients with endometrioid-type endometrial carcinoma. We also evaluated the differences in RRBP1 expression between endometrial cancer samples (n = 35) and normal endometrial tissues (n = 19) by western blotting. RESULTS: RRBP1 was more highly expressed in endometrial cancer samples than in normal samples (P < 0.05). High levels of expression of RRBP1 were strongly correlated with pathological features, such as the Federation of Gynecology and Obstetrics (FIGO) stage, histological grade, depth of myometrial invasion and lymph node metastasis (P < 0.05). Furthermore, RRBP1 expression was an independent prognostic factor for overall survival (OS) and disease-free survival (DFS) in patients with EC (both P < 0.05). CONCLUSION: This experiment identifies the utility of RRBP1 in predicting EC prognosis, revealing that it may be a potential target for therapeutics of EC. BioMed Central 2019-01-26 /pmc/articles/PMC6347782/ /pubmed/30684972 http://dx.doi.org/10.1186/s13000-019-0784-6 Text en © The Author(s). 2019 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 Liu, Shuang Lin, Mu Ji, Hongying Ding, Jing Zhu, Jiaqi Ma, Rong Meng, Fanling RRBP1 overexpression is associated with progression and prognosis in endometrial endometrioid adenocarcinoma |
title | RRBP1 overexpression is associated with progression and prognosis in endometrial endometrioid adenocarcinoma |
title_full | RRBP1 overexpression is associated with progression and prognosis in endometrial endometrioid adenocarcinoma |
title_fullStr | RRBP1 overexpression is associated with progression and prognosis in endometrial endometrioid adenocarcinoma |
title_full_unstemmed | RRBP1 overexpression is associated with progression and prognosis in endometrial endometrioid adenocarcinoma |
title_short | RRBP1 overexpression is associated with progression and prognosis in endometrial endometrioid adenocarcinoma |
title_sort | rrbp1 overexpression is associated with progression and prognosis in endometrial endometrioid adenocarcinoma |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6347782/ https://www.ncbi.nlm.nih.gov/pubmed/30684972 http://dx.doi.org/10.1186/s13000-019-0784-6 |
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