The significance of thymidine phosphorylase/platelet-derived endothelial cell growth factor activity in renal cell carcinoma
โ Scribed by Yoichi Mizutani; Hiromi Wada; Osamu Yoshida; Masakazu Fukushima; Akihiro Kawauchi; Masahiro Nakao; Tsuneharu Miki
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 88 KB
- Volume
- 98
- Category
- Article
- ISSN
- 0008-543X
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โฆ Synopsis
Abstract
BACKGROUND
Thymidine phosphorylase (TP) is identical to plateletโderived endothelial cell growth factor (PDECGF) and has angiogenic activity. Little is known about the significance of TP/PDECGF activity in patients with renal cell carcinoma (RCC). The authors examined the enzymatic activity of TP in 66 RCC specimens and investigated the association between the level of TP activity and the stage/grade status of patients with RCC. Furthermore, the authors examined the correlation between TP/PDECGF activity and prognosis.
METHODS
TP activity levels in nonfixed, freshโfrozen RCC specimens and in specimens of normal kidney were determined using a thinโlayer chromatography assay.
RESULTS
The activity of TP was approximately 3.5โfold greater in RCC specimens compared with normal kidney specimens. TP activity in patients with Stage IIIโIV RCC was 2.6โfold greater compared with TP activity in patients with Stage IโII RCC. In addition, the level of TP activity was correlated with a higher grade of RCC. Patients who had RCC with low TP activity had a longer postoperative diseaseโspecific survival compared with patients who had RCC with high TP activity in the 5โyear followโup.
CONCLUSIONS
The current study is the first to demonstrate a correlation between levels of TP activity and both disease progression and a higher grade of RCC. It also is the first to show that elevated TP activity in patients with RCC predicts a poor prognosis. The results suggest that high TP/PDECGF activity may be associated with the malignant potential of RCC and that TP/PDECGF may be a molecular therapeutic target in patients with RCC. Cancer 2003;98:730โ6. ยฉ 2003 American Cancer Society.
DOI 10.1002/cncr.11570
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