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Thymidine phosphorylase expression causes both the increase of intratumoral microvessels and decrease of apoptosis in
1First Department of Pathology, Faculty of Medicine, Tottori University, 86 Nishi-cho, Yonago, Tottori 683-8503, Japan.
Pathology International
|May 1, 2001
Summary
Thymidine phosphorylase (dThdPase) promotes esophageal squamous cell carcinoma (SCC) growth by increasing tumor blood vessels and reducing cell death. This enzyme
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Thymidine phosphorylase (dThdPase), also known as platelet-derived endothelial cell growth factor, is upregulated in various human carcinomas.
- Elevated dThdPase expression correlates with increased intratumoral microvessel density (IMVD) and poorer patient prognosis.
Purpose of the Study:
- To investigate the role of dThdPase in apoptosis, IMVD, P53 expression, and patient prognosis in human stages II and III esophageal squamous cell carcinomas (SCC).
Main Methods:
- dThdPase expression was assessed in 78 esophageal SCC samples.
- Intratumoral microvessel density (IMVD) and apoptotic index (AI) were quantified.
- P53 expression and postoperative survival rates were analyzed in relation to dThdPase status.
Main Results:
- dThdPase was expressed in 66.7% of esophageal SCC cases.
- dThdPase-positive SCC showed significantly higher IMVD and lower AI compared to dThdPase-negative cases.
- No significant difference in P53 expression or postoperative survival was observed between the groups.
- A significant inverse correlation was found between AI and IMVD (r = -0.31, P = 0.005).
Conclusions:
- dThdPase expression in esophageal SCC is associated with increased tumor vascularization and reduced apoptosis, suggesting a role in tumor growth.
- Despite not being directly linked to patient prognosis in this study, dThdPase may facilitate tumor progression through a p53-independent pathway.
- Targeting dThdPase could be a potential therapeutic strategy for esophageal SCC.