Lee A H, Dublin E A, Bobrow L G, Poulsom R
Hedley Atkins Pathology Laboratory, Imperial Cancer Research Fund Clinical Oncology Unit, Guy's Hospital, London, U.K.
J Pathol. 1998 Aug;185(4):394-401. doi: 10.1002/(SICI)1096-9896(199808)185:4<394::AID-PATH117>3.0.CO;2-S.
Angiogenesis is essential for tumour growth and important in tumour metastasis and prognosis. Vascular endothelial growth factor (VEGF) stimulates endothelial proliferation in vitro and angiogenesis in vivo. VEGF expression has been correlated with high vascularity in tumours, including carcinoma of the breast. This study investigated VEGF expression and vascularity of invasive lobular (n = 10) and invasive ductal carcinoma (n = 28), and pure ductal carcinoma in situ of the breast (n = 33). VEGF protein expression was studied with immunohistochemistry and VEGF mRNA with in situ hybridization. Vascular density was assessed on sections stained for von Willebrand factor. There was more expression of both VEGF protein (P = 0.006) and mRNA (P = 0.002) in invasive ductal than in invasive lobular carcinoma. VEGF protein (rs = 0.32, P = 0.047) and mRNA (rs = 0.56, P = 0.04) correlated with vascular density in invasive ductal carcinoma. In invasive lobular carcinoma, vascular density did not correlate with VEGF mRNA (rs = 0.15, P = 0.35) and was inversely related to VEGF protein (rs = -0.57, P = 0.04). There were no significant differences in vascular density between the two types of invasive carcinoma, suggesting that VEGF is important in angiogenesis in invasive ductal carcinoma, but that other angiogenic factors are important in invasive lobular carcinoma. Although VEGF protein was frequently expressed in ductal carcinoma in situ, no relationship was found between VEGF and the two patterns of angiogenesis previously described.
血管生成对于肿瘤生长至关重要,在肿瘤转移和预后方面也具有重要意义。血管内皮生长因子(VEGF)在体外可刺激内皮细胞增殖,在体内可促进血管生成。VEGF的表达与肿瘤的高血管化相关,包括乳腺癌。本研究调查了乳腺浸润性小叶癌(n = 10)、浸润性导管癌(n = 28)和单纯导管原位癌(n = 33)的VEGF表达及血管生成情况。采用免疫组织化学方法研究VEGF蛋白表达,采用原位杂交方法研究VEGF mRNA。通过对von Willebrand因子染色的切片评估血管密度。浸润性导管癌中VEGF蛋白(P = 0.006)和mRNA(P = 0.002)的表达均高于浸润性小叶癌。在浸润性导管癌中,VEGF蛋白(rs = 0.32,P = 0.047)和mRNA(rs = 0.56,P = 0.04)与血管密度相关。在浸润性小叶癌中,血管密度与VEGF mRNA不相关(rs = 0.15,P = 0.35),与VEGF蛋白呈负相关(rs = -0.57,P = 0.04)。两种浸润性癌之间的血管密度无显著差异,这表明VEGF在浸润性导管癌的血管生成中起重要作用,但其他血管生成因子在浸润性小叶癌中起重要作用。虽然VEGF蛋白在导管原位癌中经常表达,但未发现VEGF与先前描述的两种血管生成模式之间存在关联。