Significance of Monocyte Chemotactic Protein-1 and Thymidine Phosphorylase in Angiogenesis of Human Cardiac Myxoma.
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- Zhang Tianshu
- Second Department of Surgery, Shinshu University School of Medicine
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- Koide Naohiko
- Second Department of Surgery, Shinshu University School of Medicine
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- Wada Yuko
- Second Department of Surgery, Shinshu University School of Medicine
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- Tsukioka Katsuaki
- Second Department of Surgery, Shinshu University School of Medicine
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- Takayama Kei
- Second Department of Surgery, Shinshu University School of Medicine
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- Kono Tetsuya
- Second Department of Surgery, Shinshu University School of Medicine
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- Kitahara Hiroto
- Second Department of Surgery, Shinshu University School of Medicine
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- Amano Jun
- Second Department of Surgery, Shinshu University School of Medicine
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抄録
Angiogenesis is indispensable to tumor development and proliferation. The aim of this study was to investigate whether the expression of monocyte chemotactic protein-1 (MCP-1) and of thymidine phosphorylase (TP) correlates with the angiogenesis and clinicopathologic features in cardiac myxoma. Paraffin-embedded specimens of 17 resected cardiac myxomas were immunohistochemically stained for MCP-1, CC chemokine receptor-2 (CCR-2), TP, CD31, and CD68. Correlations among MCP-1 expression, TP expression, microvessel count (determined by CD31 staining), macrophage count (determined by CD68 staining), and the clinicopathologic features of the patients were analyzed statistically. Immunohistochemical analysis revealed that MCP-1 and TP were expressed in myxoma cells, as well as in stromal cells such as infiltrating cells, fibroblast-like cells and endothelial cells. CCR-2 was abundantly expressed in stromal infiltrating cells in all myxomas and occasionally in the endothelial cells. In the tumor stroma, the major source of MCP-1, TP and CCR-2 was macrophages, and the sites of positive staining for MCP-1, TP and CCR-2 matched in most of the myxomas. Statistical analysis revealed that the proportions of MCP-1-positive myxoma and stromal cells, and TP-positive myxoma and stromal cells significantly correlated with increased microvessel count. The proportions of MCP-1-positive myxoma and stromal cells significantly correlated with the proportion of TP-positive stromal cells. The mean microvessel count in myxomas with both high tumor and high stromal MCP-1 or TP expression was significantly higher than that in myxomas with low tumor and low stromal MCP-1 or TP expression. Small tumors (≤55 mm in diameter) exhibited high MCP-1 or TP expression, and the microvessel count in small tumors was significantly higher than in large myxomas. Although the difference was not significant, myxomas with both high tumor and high stromal MCP-1 expression had a higher macrophage count than other myxomas. These results indicate that in cardiac myxoma, MCP-1 and TP may be regarded as important angiogenic signals accompanying growth. (Circ J 2003; 67: 54 - 60)<br>
収録刊行物
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- Circulation Journal
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Circulation Journal 67 (1), 54-60, 2003
一般社団法人 日本循環器学会
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詳細情報 詳細情報について
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- CRID
- 1390001205104078848
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- NII論文ID
- 110002666209
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- NII書誌ID
- AA11591968
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- COI
- 1:CAS:528:DC%2BD3sXlt1Sluw%3D%3D
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- ISSN
- 13474820
- 13469843
- http://id.crossref.org/issn/13469843
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- PubMed
- 12520153
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- Crossref
- PubMed
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可