Budget Amount *help |
¥2,700,000 (Direct Cost: ¥2,700,000)
Fiscal Year 1998: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1997: ¥1,900,000 (Direct Cost: ¥1,900,000)
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Research Abstract |
BACKGROUND.This study was designed to evaluate the significance of tumor angiogenesis and anglogenic factors such as hepatocyte growth factor (HGF) and c-Metin determining the prognoses of 93 patients with endometrial carcinoma. METHODS.By immunohistochemical staining, this retrospective study Investigated tumor angiogenesis. HGF expression, and c-Met expression, using one tissue slide that was representative of the invasive edge of the tumor. To evaluate tumor angiogenesis, the microvessels within the primary endometrial carcinoma were highlighted by staining their endothelial cells immunohistochemically for von Wil-lebrand factor (VWF). The microvessels were then counted in the most intense areas of neovascularization. HGF and c-Met were identified with specific antibodies. Tumor angiogenesis, HGF expression, and c-Met expression were correlated with both the prognostic variables for and the survival of endometrial carcinoma. RESULTS.A high microvessel count (<greater than or equal> 110 in a 0.90 mm^2 area) was significantly correlated with surgical Stage ill and IV, histologic Grade 3, positive lymph node involvement, and shorter patient survival. Expression of c-Met was significantly correlated with surgical Stage III andIV, histologic Grade 3, and shorter survival. HGF expression was significantly correlated with surgical Stage.III and IV by semi-quantitative analysis. Multivariate analysis showed that surgical Stage III and IV, histologic Grade 3, the score for myometrial invasion >1/2, and a high microvesselcount were independent Indicators of the prognoses of patients with endometrialcarcinom CONCLUSIONS.Both tumor angiogenesls. measured by the microvessel count, andc-Met expression were significant prognostic indicators for patients with endometrial carcinoma.
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