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High expression of metabolic enzyme PFKFB4 is associated with poor prognosis of operable breast cancer

BACKGROUND: Enhanced glycolysis in tumors, known as the Warburg effect, provides the metabolic basis of enhanced cancer cell proliferation and metastasis. The Warburg pathway enzyme 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 4 (PFKFB4) is a newly identified key kinase that regulates transc...

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Autores principales: Yao, Ling, Wang, Lei, Cao, Zhi-Gang, Hu, Xin, Shao, Zhi-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582605/
https://www.ncbi.nlm.nih.gov/pubmed/31244553
http://dx.doi.org/10.1186/s12935-019-0882-2
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author Yao, Ling
Wang, Lei
Cao, Zhi-Gang
Hu, Xin
Shao, Zhi-Ming
author_facet Yao, Ling
Wang, Lei
Cao, Zhi-Gang
Hu, Xin
Shao, Zhi-Ming
author_sort Yao, Ling
collection PubMed
description BACKGROUND: Enhanced glycolysis in tumors, known as the Warburg effect, provides the metabolic basis of enhanced cancer cell proliferation and metastasis. The Warburg pathway enzyme 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 4 (PFKFB4) is a newly identified key kinase that regulates transcriptional reprogramming and cell proliferation. Here we show the prognostic value of PFKFB4 expression in patients with operable breast cancer. METHODS: PFKFB4 expression was evaluated by immunohistochemistry in surgical specimens retrospectively collected from 200 patients with histologically proven invasive ductal breast cancer. Kaplan–Meier survival analysis and Cox regression analysis were performed to assess the prognostic significance of PFKFB4 expression. RESULTS: Kaplan–Meier survival analysis revealed that breast cancer patients with high PFKFB4 expression demonstrated unfavorable disease-free survival (p = 0.008) and overall survival (p = 0.002). PFKFB4 had an hazard ratio (HR) of 7.38 (95% CI 1.69–32.3; p = 0.008) in univariate Cox analysis and retained prognostic power (HR 7.44, 95% CI 1.67–33.2; p = 0.009) when adjusted by tumor size, lymph node status, grade, estrogen receptor status, human epidermal growth factor receptor 2 status and subtype, which indicated PFKFB4 was an independent prognostic factor in breast cancer. CONCLUSIONS: Together, our findings establish the prognostic value of metabolic enzyme PFKFB4 in patients with operable breast cancer. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12935-019-0882-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-65826052019-06-26 High expression of metabolic enzyme PFKFB4 is associated with poor prognosis of operable breast cancer Yao, Ling Wang, Lei Cao, Zhi-Gang Hu, Xin Shao, Zhi-Ming Cancer Cell Int Primary Research BACKGROUND: Enhanced glycolysis in tumors, known as the Warburg effect, provides the metabolic basis of enhanced cancer cell proliferation and metastasis. The Warburg pathway enzyme 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 4 (PFKFB4) is a newly identified key kinase that regulates transcriptional reprogramming and cell proliferation. Here we show the prognostic value of PFKFB4 expression in patients with operable breast cancer. METHODS: PFKFB4 expression was evaluated by immunohistochemistry in surgical specimens retrospectively collected from 200 patients with histologically proven invasive ductal breast cancer. Kaplan–Meier survival analysis and Cox regression analysis were performed to assess the prognostic significance of PFKFB4 expression. RESULTS: Kaplan–Meier survival analysis revealed that breast cancer patients with high PFKFB4 expression demonstrated unfavorable disease-free survival (p = 0.008) and overall survival (p = 0.002). PFKFB4 had an hazard ratio (HR) of 7.38 (95% CI 1.69–32.3; p = 0.008) in univariate Cox analysis and retained prognostic power (HR 7.44, 95% CI 1.67–33.2; p = 0.009) when adjusted by tumor size, lymph node status, grade, estrogen receptor status, human epidermal growth factor receptor 2 status and subtype, which indicated PFKFB4 was an independent prognostic factor in breast cancer. CONCLUSIONS: Together, our findings establish the prognostic value of metabolic enzyme PFKFB4 in patients with operable breast cancer. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12935-019-0882-2) contains supplementary material, which is available to authorized users. BioMed Central 2019-06-18 /pmc/articles/PMC6582605/ /pubmed/31244553 http://dx.doi.org/10.1186/s12935-019-0882-2 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 Primary Research
Yao, Ling
Wang, Lei
Cao, Zhi-Gang
Hu, Xin
Shao, Zhi-Ming
High expression of metabolic enzyme PFKFB4 is associated with poor prognosis of operable breast cancer
title High expression of metabolic enzyme PFKFB4 is associated with poor prognosis of operable breast cancer
title_full High expression of metabolic enzyme PFKFB4 is associated with poor prognosis of operable breast cancer
title_fullStr High expression of metabolic enzyme PFKFB4 is associated with poor prognosis of operable breast cancer
title_full_unstemmed High expression of metabolic enzyme PFKFB4 is associated with poor prognosis of operable breast cancer
title_short High expression of metabolic enzyme PFKFB4 is associated with poor prognosis of operable breast cancer
title_sort high expression of metabolic enzyme pfkfb4 is associated with poor prognosis of operable breast cancer
topic Primary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582605/
https://www.ncbi.nlm.nih.gov/pubmed/31244553
http://dx.doi.org/10.1186/s12935-019-0882-2
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