Xie Xiao-Dong, Qu Shu-Xian, Zheng Zhen-Dong, Song Fu-Lin, Liu Da-Wei
Department of Oncology, General Hospital of Shenyang Military Region, Shenyang 110016, China.
Zhonghua Zhong Liu Za Zhi. 2008 May;30(5):356-60.
To investigate the relationship of lymphatic micovessel density (LMVD) detected by monoclonal antibody D2-40) with the VEGF-C expression in human breast cancer.
Tissue samples of 102 breast cancers, 25 breast fibroadenomas and 10 normal breasts were collected. Immunohistochemical staining was used to detected the lymphatic micovessels with monoclonal antibody D2-40. The expression of VEGF-C was detect by SP immunohistochemistry, and VEGF-C mRNA by hybridization in situ.
In 102 breast cancers, the positive rate of D2-40 was 76.5% (78/102), higher than that in the breast fibroadenomas. LMVD in the periphery of breast cancer was 30.1 lymphatic microvessels per x 100 field of vision, which was significantly higher than that in the central area of the tumors (P = 0.000). The LMVD in the periphery of the breast cancers was correlated with the number of metastatic lymph nodes (r = 0.964, P < 0.01). The positive rates of VEGF-C protein and mRNA were 55.9% (57/102) and 59.8% (61/102), respectively, significantly higher than that in the breast fiberoadenomas and normal breast tissues (chi2 = 11.653, P = 0.003; chi2 = 10.345, P = 0.006), and were significantly correlated with the status of lymph node metastasis, clinical stage and the expressions of c-erbB-2 and p53 protein (P < 0.05). Both of VEGF-C protein and mRNA were significantly correlated with LMVD detected by D2-40 (P < 0.05), especially with the LMVD in the periphery of breast cancers (P < 0.05).
The monoclonal antibody D240 can be used to detect the lymphatic endothelium in human breast cancer. The lymphatic microvessel density in the periphery of breast cancer is correlated with the lymph node metastasis and expression of VEGF-C. Therefore, VEGF-C may play a significant role in the lymphangiogenesis leading to metastasis of breast cancer.
探讨单克隆抗体D2-40检测的淋巴管微血管密度(LMVD)与人乳腺癌中VEGF-C表达的关系。
收集102例乳腺癌、25例乳腺纤维腺瘤和10例正常乳腺的组织样本。采用免疫组织化学染色法用单克隆抗体D2-40检测淋巴管微血管。采用SP免疫组织化学法检测VEGF-C的表达,原位杂交法检测VEGF-C mRNA。
102例乳腺癌中,D2-40阳性率为76.5%(78/102),高于乳腺纤维腺瘤。乳腺癌周边的LMVD为每100视野30.1个淋巴管微血管,显著高于肿瘤中心区域(P = 0.000)。乳腺癌周边的LMVD与腋窝淋巴结转移数相关(r = 0.964,P < 0.01)。VEGF-C蛋白和mRNA的阳性率分别为55.9%(57/102)和59.8%(61/102),显著高于乳腺纤维腺瘤和正常乳腺组织(χ2 = 11.653,P = 0.003;χ2 = 10.345,P = 0.006),且与腋窝淋巴结转移状态、临床分期及c-erbB-2和p53蛋白表达显著相关(P < 0.05)。VEGF-C蛋白和mRNA均与D2-40检测的LMVD显著相关(P < 0.05),尤其与乳腺癌周边的LMVD相关(P < 0.05)。
单克隆抗体D240可用于检测人乳腺癌中的淋巴管内皮。乳腺癌周边的淋巴管微血管密度与腋窝淋巴结转移及VEGF-C表达相关。因此,VEGF-C可能在导致乳腺癌转移的淋巴管生成中起重要作用。