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Is Red Cell Distribution Width a Novel Biomarker of Breast Cancer Activity? Data From a Pilot Study
BACKGROUND: Red cell distribution width (RDW) is a parameter of the standard full blood count tests, measuring the size variability of erythrocytes. Recently, its elevation has been proven to reliably reflect the extent systematic inflammation, mainly in cardiometabolic diseases. Up to date, its ass...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elmer Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3601498/ https://www.ncbi.nlm.nih.gov/pubmed/23518817 http://dx.doi.org/10.4021/jocmr1214w |
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author | Seretis, Charalampos Seretis, Fotios Lagoudianakis, Emmanouil Gemenetzis, George Salemis, Nikolaos S. |
author_facet | Seretis, Charalampos Seretis, Fotios Lagoudianakis, Emmanouil Gemenetzis, George Salemis, Nikolaos S. |
author_sort | Seretis, Charalampos |
collection | PubMed |
description | BACKGROUND: Red cell distribution width (RDW) is a parameter of the standard full blood count tests, measuring the size variability of erythrocytes. Recently, its elevation has been proven to reliably reflect the extent systematic inflammation, mainly in cardiometabolic diseases. Up to date, its association with solid malignancies has been scarcely investigated. METHODS: We performed a retrospective study, in order to examine if RDW values comparing elevation is correlated with the histopathological parameters of breast cancer (tumor size, grade, lymphatic spread, overexpression of hormonal receptors and HER2 protein), as well as to assess the existence of any differences in RDW comparing two age-matched groups of patients with benign and malignant breast lesions respectively. RESULTS: RDW was significantly higher in patients with breast cancer, when compared to the enrolled patients with fibroadenomas. Moreover, in the breast cancer group, RDW elevation was significantly correlated with larger primary tumors, higher number of infiltrated axillary lymph nodes and HER2 overexpression, while it was inversely associated with the tumor grade. CONCLUSIONS: Our pilot study demonstrated tha Red cell distribution width may be a novel biomarker of the activity of breast cancer. Although our preliminary findings need to be evaluated by studies with larger samples of patients, based on commonly accepted pathophysiological principles, we presume that they will be applicable not only in breast cancer, but also in other types of solid cancers, providing a simple and cost-effective biomarker of cancer surveillance. |
format | Online Article Text |
id | pubmed-3601498 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elmer Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-36014982013-03-21 Is Red Cell Distribution Width a Novel Biomarker of Breast Cancer Activity? Data From a Pilot Study Seretis, Charalampos Seretis, Fotios Lagoudianakis, Emmanouil Gemenetzis, George Salemis, Nikolaos S. J Clin Med Res Original Article BACKGROUND: Red cell distribution width (RDW) is a parameter of the standard full blood count tests, measuring the size variability of erythrocytes. Recently, its elevation has been proven to reliably reflect the extent systematic inflammation, mainly in cardiometabolic diseases. Up to date, its association with solid malignancies has been scarcely investigated. METHODS: We performed a retrospective study, in order to examine if RDW values comparing elevation is correlated with the histopathological parameters of breast cancer (tumor size, grade, lymphatic spread, overexpression of hormonal receptors and HER2 protein), as well as to assess the existence of any differences in RDW comparing two age-matched groups of patients with benign and malignant breast lesions respectively. RESULTS: RDW was significantly higher in patients with breast cancer, when compared to the enrolled patients with fibroadenomas. Moreover, in the breast cancer group, RDW elevation was significantly correlated with larger primary tumors, higher number of infiltrated axillary lymph nodes and HER2 overexpression, while it was inversely associated with the tumor grade. CONCLUSIONS: Our pilot study demonstrated tha Red cell distribution width may be a novel biomarker of the activity of breast cancer. Although our preliminary findings need to be evaluated by studies with larger samples of patients, based on commonly accepted pathophysiological principles, we presume that they will be applicable not only in breast cancer, but also in other types of solid cancers, providing a simple and cost-effective biomarker of cancer surveillance. Elmer Press 2013-04 2013-02-25 /pmc/articles/PMC3601498/ /pubmed/23518817 http://dx.doi.org/10.4021/jocmr1214w Text en Copyright 2013, Seretis et al. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Seretis, Charalampos Seretis, Fotios Lagoudianakis, Emmanouil Gemenetzis, George Salemis, Nikolaos S. Is Red Cell Distribution Width a Novel Biomarker of Breast Cancer Activity? Data From a Pilot Study |
title | Is Red Cell Distribution Width a Novel Biomarker of Breast Cancer Activity? Data From a Pilot Study |
title_full | Is Red Cell Distribution Width a Novel Biomarker of Breast Cancer Activity? Data From a Pilot Study |
title_fullStr | Is Red Cell Distribution Width a Novel Biomarker of Breast Cancer Activity? Data From a Pilot Study |
title_full_unstemmed | Is Red Cell Distribution Width a Novel Biomarker of Breast Cancer Activity? Data From a Pilot Study |
title_short | Is Red Cell Distribution Width a Novel Biomarker of Breast Cancer Activity? Data From a Pilot Study |
title_sort | is red cell distribution width a novel biomarker of breast cancer activity? data from a pilot study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3601498/ https://www.ncbi.nlm.nih.gov/pubmed/23518817 http://dx.doi.org/10.4021/jocmr1214w |
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