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Increased number and function of endothelial progenitor cells in breast cancer patients and the linear correlation with VEGF level

Zhen-Hua Huang, Zhao-Xia Tang, Rui-Bin Cai, Feng Ye, Min-Qing Wu,  Dan Zhang,  Zhihao Liu

Abstract:

The number of circulating endothelial progenitor cells (EPCs) was found to increase in patients with breast cancer, but the alteration in EPC function remains to be elusive. We conducted this study to evaluate the number and function of peripheral EPCs of breast cancer patients and its possible underlying mechanism. Besides, the vascular endothelial growth factor (VEGF), VCAM-1, IL-6, and IL-34 levels were measured in blood samples and also in vitro in a medium of EPCs. We found that the number of circulating EPCs in breast cancer patients was significantly higher than that in normal control and remarkably augmented in a stage-dependent manner. Meanwhile, a similar enhancement was observed in the migratory, proliferative, and adhesive activity of circulating EPCs originating from breast cancer patients. More importantly, the VEGF level in blood samples was dramatically elevated in comparison to the control, which was correlated positively with the number and activity of circulating EPCs from breast cancer patients. Moreover, in vitro medium of EPCs from breast cancer patients highly expressed VEGF compared with that from the control, which also had a positive correlation with the number and activity of circulating EPCs from breast cancer patients. This is the first time to demonstrate that the number and function of circulating EPCs are promoted in breast cancer patients, which are positively related to an enhanced VEGF production. These may provide a novel target for improving the outcome of breast cancer.

Received date: 06/15/2021

Accepted date: 08/09/2021

Ahead of print publish date: 01/12/2022

Issue: 1/2022

Volume: 69

Pages: 242 — 250

Keywords: endothelial progenitor cells, breast cancer, vascular endothelial growth factor

Supplementary files:
N800 Suppl Figure Legends-TE1.doc
N800 Suppl FigS1-TE1.tif

DOI: 10.4149/neo_2021_210615N800

Pubmed

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