Expression of cell adhesion molecules E-, P-, N-cadherin-6, -11, and -13 in renal cell carcinomas. An immunohistochemical study
Expression of cell adhesion molecules E-, P-, N-cadherin-6, -11, and -13 in renal cell carcinomas. An immunohistochemical study
批准号:
09671651
负责人:
ASAKURA Hirotaka
金额:
$2.05万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1997
资助国家:
日本
项目状态:
已结题
起止时间:
1997 至 1999
中文摘要
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英文摘要
Expression of six cadherin molecules, E-, P-, N-cadherin, cadhelin-6,-11, and -13, in renal cell carcinomas (RCC), was investigated in order to elucidate whether these molecules are involved in the progression. Northern blot analysis of seven RCC cell lines showed that N-cadherin and cadhelin-6 were strongly expressed in all and 5 lines, respectively, whereas E, and P-cadherin were not detected at all. In KU2 cells transplanted to SCID mice, N-cadherin and cadhelin-6 were detected faintly in the subcutaneous tumors, but not in the metastatic tumors. Each cadherin expression in 30 surgically resected RCC was examined by immunostaining using frozen sections. The number of tumors expressing E-cadherin was significantly smaller than that of N-cadherin or cadhelin-6 (p<0.005). High grade tumors tended to have neither E-cadherin nor cadhelin-6 expression. In five metastatic tumors to the lung, cadhelin-6 was expressed in all, N-cadherin in 4, but E-cadherin in one. Using paraffin-embedded specimens of surgically resected RCC, expression of E- and N-cadherin was also examined immunohistochemically, and correlation between pathological tumor extension (pT classification) and the cadherin expression was analyzed. The patterns of each cadherin expression were almost the same as those in the aforementioned frozen specimens. In 10 primary tumors having metastatic lesions, N- and E-cadherin were detected in 8 and 4, respectively, and coexpression of E- and N-cadherin was observed in 3 tumors. High pT tumors tended to have N-cadherin expression. These results suggested that expression of N-cadherin or cadhelin-6, and absence of E-cadhelin expression might be correlated to the progression of RCC, although further studies will be necessary to draw. A conclusion
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会议论文
Tachibana M,et al: "Role of proliferative activity estimated by bromodeoxyuridine labeling index in determining predictive factors recurrence in superficial intermediately malignant bladder tumors." Journal of Urology. 156(1). 63-69 (1997)
Tachibana M 等人:“通过溴脱氧尿苷标记指数估计的增殖活性在确定浅表中度恶性膀胱肿瘤复发的预测因素中的作用。”
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影响因子:
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通讯作者:
Tachibana M,et al: "Constituve production of multiple cytokines and a human chorionic gonadotrophin beta-subunit by a human bladder cancer cell line (KU-19-19) : possible demonstration of totipotential differentiation." British Journal of Cancer. 76(2). 1
Tachibana M 等人:“人膀胱癌细胞系 (KU-19-19) 持续产生多种细胞因子和人绒毛膜促性腺激素 β 亚基:可能证明全能分化。”
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Tachibana M,et al: "Granulocyte colony-stimulating factor receptor expression on human transitional cell carcinoma of the bladder." British Journal of Cancer. 75(10). 1489-1496 (1997)
Tachibana M 等人:“人膀胱移行细胞癌中粒细胞集落刺激因子受体的表达。”
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Enhanced effect of combination chemotherapy based on induction of proliferative activity for advanceduro thelial cancers.
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批准号:08671843
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$1.41万
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财政年份:1996
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负责人:ASAKURA Hirotaka
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依托单位:
国内基金
海外基金
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