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Differences in Circulating Endothelial Progenitor Cells among Childhood Cancer Survivors Treated with and without Radiation
Radiation during childhood cancer treatment increases the propensity to atherosclerotic cardiovascular disease among adult survivors of childhood cancer. This is thought to be mediated through the damage to the underlying vascular endothelium. Endothelial progenitor cells (EPCs) involved in vascular...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4627707/ https://www.ncbi.nlm.nih.gov/pubmed/26523291 http://dx.doi.org/10.13188/2380-6842.1000005 |
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author | Pradhan, Kamnesh Mund, Julie Case, Jamie Gupta, Samir Liu, Ziyue Gathirua-Mwangi, Wambui McDaniel, Anna Renbarger, Jamie Champion, Victoria |
author_facet | Pradhan, Kamnesh Mund, Julie Case, Jamie Gupta, Samir Liu, Ziyue Gathirua-Mwangi, Wambui McDaniel, Anna Renbarger, Jamie Champion, Victoria |
author_sort | Pradhan, Kamnesh |
collection | PubMed |
description | Radiation during childhood cancer treatment increases the propensity to atherosclerotic cardiovascular disease among adult survivors of childhood cancer. This is thought to be mediated through the damage to the underlying vascular endothelium. Endothelial progenitor cells (EPCs) involved in vascular endothelial repair after its damage may be affected by radiation therapy but have never been investigated in adult survivors of childhood cancer. In this pilot study, utilizing multi-parametric flowcytometry, endothelial colony forming cells (ECFCs), which are the bonafide EPCs, and circulating endothelial cells (CECs), which are not EPCs, were compared between adult survivors of childhood cancer with or without radiation exposure. In addition, their associations with blood-pressure, physical activity and diet were examined. Survivors who received radiotherapy had lower ECFCs and CECs (p<0.05) compared to those without it. Significant positive correlations included physical activity with ECFCs and diet with CECs, while blood-pressure negatively correlated with ECFCs. Further evaluation is needed to examine the effect of radiation and modifiable risk factors on ECFCs and CECs. The preliminary findings from this study suggest evidence of the role of ECFCs as biomarkers of vascular injury following treatment for childhood cancer that may help in early identification of survivors at risk for cardiovascular disease. |
format | Online Article Text |
id | pubmed-4627707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
record_format | MEDLINE/PubMed |
spelling | pubmed-46277072015-10-30 Differences in Circulating Endothelial Progenitor Cells among Childhood Cancer Survivors Treated with and without Radiation Pradhan, Kamnesh Mund, Julie Case, Jamie Gupta, Samir Liu, Ziyue Gathirua-Mwangi, Wambui McDaniel, Anna Renbarger, Jamie Champion, Victoria J Hematol Thromb Article Radiation during childhood cancer treatment increases the propensity to atherosclerotic cardiovascular disease among adult survivors of childhood cancer. This is thought to be mediated through the damage to the underlying vascular endothelium. Endothelial progenitor cells (EPCs) involved in vascular endothelial repair after its damage may be affected by radiation therapy but have never been investigated in adult survivors of childhood cancer. In this pilot study, utilizing multi-parametric flowcytometry, endothelial colony forming cells (ECFCs), which are the bonafide EPCs, and circulating endothelial cells (CECs), which are not EPCs, were compared between adult survivors of childhood cancer with or without radiation exposure. In addition, their associations with blood-pressure, physical activity and diet were examined. Survivors who received radiotherapy had lower ECFCs and CECs (p<0.05) compared to those without it. Significant positive correlations included physical activity with ECFCs and diet with CECs, while blood-pressure negatively correlated with ECFCs. Further evaluation is needed to examine the effect of radiation and modifiable risk factors on ECFCs and CECs. The preliminary findings from this study suggest evidence of the role of ECFCs as biomarkers of vascular injury following treatment for childhood cancer that may help in early identification of survivors at risk for cardiovascular disease. 2015-08-05 2015-08 /pmc/articles/PMC4627707/ /pubmed/26523291 http://dx.doi.org/10.13188/2380-6842.1000005 Text en http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Pradhan, Kamnesh Mund, Julie Case, Jamie Gupta, Samir Liu, Ziyue Gathirua-Mwangi, Wambui McDaniel, Anna Renbarger, Jamie Champion, Victoria Differences in Circulating Endothelial Progenitor Cells among Childhood Cancer Survivors Treated with and without Radiation |
title | Differences in Circulating Endothelial Progenitor Cells among Childhood Cancer Survivors Treated with and without Radiation |
title_full | Differences in Circulating Endothelial Progenitor Cells among Childhood Cancer Survivors Treated with and without Radiation |
title_fullStr | Differences in Circulating Endothelial Progenitor Cells among Childhood Cancer Survivors Treated with and without Radiation |
title_full_unstemmed | Differences in Circulating Endothelial Progenitor Cells among Childhood Cancer Survivors Treated with and without Radiation |
title_short | Differences in Circulating Endothelial Progenitor Cells among Childhood Cancer Survivors Treated with and without Radiation |
title_sort | differences in circulating endothelial progenitor cells among childhood cancer survivors treated with and without radiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4627707/ https://www.ncbi.nlm.nih.gov/pubmed/26523291 http://dx.doi.org/10.13188/2380-6842.1000005 |
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