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STAT3, a Poor Survival Predicator, Is Associated with Lymph Node Metastasis from Breast Cancer
PURPOSE: The aim of this study is to explore signal transducer and activator of transcription 3 (STAT3) expression in breast cancer and to analyze the detailed mechanism that STAT3 contributes to the progression of breast cancer. METHODS: We retrospectively analyzed the clinicopathologic characteris...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Breast Cancer Society
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3625768/ https://www.ncbi.nlm.nih.gov/pubmed/23593080 http://dx.doi.org/10.4048/jbc.2013.16.1.40 |
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author | Chen, Yujuan Wang, Jing Wang, Xiaodong Liu, Xuejuan Li, Hongjiang Lv, Qing Zhu, Jingqiang Wei, Bing Tang, Ying |
author_facet | Chen, Yujuan Wang, Jing Wang, Xiaodong Liu, Xuejuan Li, Hongjiang Lv, Qing Zhu, Jingqiang Wei, Bing Tang, Ying |
author_sort | Chen, Yujuan |
collection | PubMed |
description | PURPOSE: The aim of this study is to explore signal transducer and activator of transcription 3 (STAT3) expression in breast cancer and to analyze the detailed mechanism that STAT3 contributes to the progression of breast cancer. METHODS: We retrospectively analyzed the clinicopathologic characteristics and overall survival (OS) of 140 breast cancer patients after curative surgery, and detected STAT3 expression, phosphorylated STAT3 (pSTAT3) expression, Ki-67 expression, vascular endothelial growth factor (VEGF)-C and -D expression in breast cancer tissues, and adjacent nontumor tissues. Survival analysis and relationship analysis were adopted for demonstrated the important mechanism of STAT3 contribution to progression of breast cancer. RESULTS: STAT3 expression, pSTAT3 expression, Ki-67 expression, VEGF-C expression, and VEGF-D expression in breast cancer tissues were significantly higher than those in adjacent nontumor tissues, respectively. With survival analysis, only number of lymph node metastasis (N stage) was identified as the independent predictors of the OS of breast cancer patients. Besides, we demonstrated there was the most prominent correlation between STAT3 expression and lymph node metastasis in breast cancer tissues by using the multinominal regression method. CONCLUSION: STAT3, a poor survival biomarker potential association with lymph node metastasis, was suitable for predication the OS of breast cancer patients after curative resection. |
format | Online Article Text |
id | pubmed-3625768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Korean Breast Cancer Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-36257682013-04-16 STAT3, a Poor Survival Predicator, Is Associated with Lymph Node Metastasis from Breast Cancer Chen, Yujuan Wang, Jing Wang, Xiaodong Liu, Xuejuan Li, Hongjiang Lv, Qing Zhu, Jingqiang Wei, Bing Tang, Ying J Breast Cancer Original Article PURPOSE: The aim of this study is to explore signal transducer and activator of transcription 3 (STAT3) expression in breast cancer and to analyze the detailed mechanism that STAT3 contributes to the progression of breast cancer. METHODS: We retrospectively analyzed the clinicopathologic characteristics and overall survival (OS) of 140 breast cancer patients after curative surgery, and detected STAT3 expression, phosphorylated STAT3 (pSTAT3) expression, Ki-67 expression, vascular endothelial growth factor (VEGF)-C and -D expression in breast cancer tissues, and adjacent nontumor tissues. Survival analysis and relationship analysis were adopted for demonstrated the important mechanism of STAT3 contribution to progression of breast cancer. RESULTS: STAT3 expression, pSTAT3 expression, Ki-67 expression, VEGF-C expression, and VEGF-D expression in breast cancer tissues were significantly higher than those in adjacent nontumor tissues, respectively. With survival analysis, only number of lymph node metastasis (N stage) was identified as the independent predictors of the OS of breast cancer patients. Besides, we demonstrated there was the most prominent correlation between STAT3 expression and lymph node metastasis in breast cancer tissues by using the multinominal regression method. CONCLUSION: STAT3, a poor survival biomarker potential association with lymph node metastasis, was suitable for predication the OS of breast cancer patients after curative resection. Korean Breast Cancer Society 2013-03 2013-03-31 /pmc/articles/PMC3625768/ /pubmed/23593080 http://dx.doi.org/10.4048/jbc.2013.16.1.40 Text en © 2013 Korean Breast Cancer Society. All rights reserved. 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 Chen, Yujuan Wang, Jing Wang, Xiaodong Liu, Xuejuan Li, Hongjiang Lv, Qing Zhu, Jingqiang Wei, Bing Tang, Ying STAT3, a Poor Survival Predicator, Is Associated with Lymph Node Metastasis from Breast Cancer |
title | STAT3, a Poor Survival Predicator, Is Associated with Lymph Node Metastasis from Breast Cancer |
title_full | STAT3, a Poor Survival Predicator, Is Associated with Lymph Node Metastasis from Breast Cancer |
title_fullStr | STAT3, a Poor Survival Predicator, Is Associated with Lymph Node Metastasis from Breast Cancer |
title_full_unstemmed | STAT3, a Poor Survival Predicator, Is Associated with Lymph Node Metastasis from Breast Cancer |
title_short | STAT3, a Poor Survival Predicator, Is Associated with Lymph Node Metastasis from Breast Cancer |
title_sort | stat3, a poor survival predicator, is associated with lymph node metastasis from breast cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3625768/ https://www.ncbi.nlm.nih.gov/pubmed/23593080 http://dx.doi.org/10.4048/jbc.2013.16.1.40 |
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