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Published in: Tumor Biology 2/2016

01-02-2016 | Original Article

Circulating CD105 shows significant impact in patients of oral cancer and promotes malignancy of cancer cells via CCL20

Authors: Chang-Han Chen, Hui-Ching Chuang, Yu-Tsai Lin, Fu-Min Fang, Chao-Cheng Huang, Ching-Mei Chen, Hui Lu, Chih-Yen Chien

Published in: Tumor Biology | Issue 2/2016

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Abstract

CD105 is rich in endothelium cells and is involved in angiogenesis. Higher microvascular density of tumor is also related to the prognosis in a variety of cancers. In this present study, patients with positive N classification, advanced T classification, advanced TNM stage, extracapsular spread of lymph nodes (ECS), and perineural invasion had significantly higher levels of peripheral vein (pCD105) and venous return from tumor (tCD105) in 71 patients with OSCC compared to 13 healthy volunteers. Those with higher pCD105 or tCD105 levels had significantly poorer 5-year disease-specific survival rate (DDS) and overall survival rate (OS). The tCD105 and pCD105 levels and ECS were the independent prognostic factors by the multivariate analysis according to the Cox regression model in 5-year DDS and OS rate. SAS and SCC4 cells treated with CD105 showed the increase in migration, invasion, and proliferation in vitro and in vivo. Furthermore, CCL20 expression participated in CD105-elicited cell motility in oral cancer cells. In conclusion, higher level of circulating CD105 is related to adverse pathological features among patients with OSCC. It is also a useful marker for evaluating the prognosis and targeting therapeutics of OSCC.
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Metadata
Title
Circulating CD105 shows significant impact in patients of oral cancer and promotes malignancy of cancer cells via CCL20
Authors
Chang-Han Chen
Hui-Ching Chuang
Yu-Tsai Lin
Fu-Min Fang
Chao-Cheng Huang
Ching-Mei Chen
Hui Lu
Chih-Yen Chien
Publication date
01-02-2016
Publisher
Springer Netherlands
Published in
Tumor Biology / Issue 2/2016
Print ISSN: 1010-4283
Electronic ISSN: 1423-0380
DOI
https://doi.org/10.1007/s13277-015-3991-0

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