Nuffield Department of Clinical Laboratory Sciences,Weatherall Institute ofMolecular Medicine, University of Oxford, Oxford, UK.
Am J Pathol. 2010 Apr;176(4):2019-28. doi: 10.2353/ajpath.2010.090908. Epub 2010 Feb 18.
Delta-like ligand 4 (Dll4) is a Notch ligand that is predominantly expressed in the endothelium. Evidence from xenografts suggests that inhibiting Dll4 may overcome resistance to antivascular endothelial growth factor therapy. The aims of this study were to characterize the expression of Dll4 in breast cancer and assess whether it is associated with inflammatory markers and prognosis. We examined 296 breast adenocarcinomas and 38 ductal carcinoma in situ tissues that were represented in tissue microarrays. Additional whole sections representing 10 breast adenocarcinomas, 10 normal breast tissues, and 16 angiosarcomas were included. Immunohistochemistry was then performed by using validated antibodies against Dll4, CD68, CD14, Dendritic Cell-Specific Intercellular adhesion molecule-3-Grabbing Non-integrin (DC-SIGN), CD123, neutrophil elastase, CD31, and carbonic anhydrase 9. Dll4 was selectively expressed by intratumoral endothelial cells in 73% to 100% of breast adenocarcinomas, 18% of in situ ductal carcinomas, and all lactating breast cases, but not normal nonlactating breast. High intensity of endothelial Dll4 expression was a statistically significant adverse prognostic factor in univariate (P = 0.002 and P = 0.01) and multivariate analyses (P = 0.03 and P = 0.04) of overall survival and relapse-free survival, respectively. Among the inflammatory markers, only CD68 and DC-SIGN were significant prognostic factors in univariate (but not multivariate) analyses of overall survival (P = 0.01 and 0.002, respectively). In summary, Dll4 was expressed by endothelium associated with breast cancer cells. In these retrospective subset analyses, endothelial Dll4 expression was a statistically significant multivariate prognostic factor.
Delta-like 配体 4(Dll4)是一种主要在血管内皮细胞中表达的 Notch 配体。来自异种移植物的证据表明,抑制 Dll4 可能克服对血管内皮生长因子治疗的耐药性。本研究的目的是研究 Dll4 在乳腺癌中的表达特征,并评估其是否与炎症标志物和预后相关。我们检查了 296 例乳腺腺癌和 38 例导管原位癌组织,这些组织代表在组织微阵列中。还包括另外 10 例乳腺腺癌、10 例正常乳腺组织和 16 例血管肉瘤的全切片。然后使用针对 Dll4、CD68、CD14、树突状细胞特异性细胞间黏附分子-3 抓取非整联蛋白(DC-SIGN)、CD123、中性粒细胞弹性蛋白酶、CD31 和碳酸酐酶 9 的验证抗体进行免疫组织化学染色。Dll4 在 73%至 100%的乳腺腺癌、18%的原位导管癌和所有哺乳期乳腺癌中选择性地表达于肿瘤内的内皮细胞,但在正常非哺乳期乳腺中不表达。内皮 Dll4 表达强度高是单因素(P = 0.002 和 P = 0.01)和多因素分析(P = 0.03 和 P = 0.04)中总生存和无复发生存的统计学显著不良预后因素。在炎症标志物中,只有 CD68 和 DC-SIGN 是总生存的单因素(但不是多因素)分析中的显著预后因素(分别为 P = 0.01 和 0.002)。总之,Dll4 由与乳腺癌细胞相关的内皮细胞表达。在这些回顾性亚组分析中,内皮 Dll4 表达是统计学上显著的多因素预后因素。