Section for Pathology, The Gade Institute, University of Bergen, Bergen, Norway.
Am J Pathol. 2011 Feb;178(2):861-71. doi: 10.1016/j.ajpath.2010.10.040.
The presence of tumor cells entering vascular channels is a prognostic marker for many cancers, including endometrial carcinoma. Vascular invasion is considered to be an early step in the metastatic process and important for the progress of malignant tumors. Here, we investigated the gene expression patterns related to vascular involvement in 57 primary endometrial cancers, using DNA microarray and quantitative PCR techniques. A vascular invasion signature of 18 genes was significantly associated with patient survival and clinicopathological phenotype. Vascular involvement was also related to gene sets for epithelial-mesenchymal transition, wound response, endothelial cells, and vascular endothelial growth factor (VEGF) activity. With immunohistochemical validation, both collagen 8 and matrix metalloproteinase 3 (MMP3) were associated with vascular invasion, whereas ANGPTL4 and IL-8 were associated with patient survival. Our findings indicate that vascular involvement within primary tumors is associated with gene expression profiles related to angiogenesis and epithelial-mesenchymal transition. These data could contribute to an improved understanding of potential targets for metastatic spread and may provide clinically important information for better management of endometrial cancer.
肿瘤细胞进入血管通道的存在是许多癌症的预后标志物,包括子宫内膜癌。血管侵犯被认为是转移过程中的早期步骤,对恶性肿瘤的进展很重要。在这里,我们使用 DNA 微阵列和定量 PCR 技术研究了 57 例原发性子宫内膜癌中与血管受累相关的基因表达模式。18 个基因的血管侵犯特征与患者生存和临床病理表型显著相关。血管受累也与上皮-间充质转化、伤口反应、内皮细胞和血管内皮生长因子 (VEGF) 活性的基因集相关。通过免疫组织化学验证,胶原 8 和基质金属蛋白酶 3 (MMP3) 均与血管侵犯相关,而 ANGPTL4 和 IL-8 与患者生存相关。我们的研究结果表明,原发性肿瘤内的血管受累与与血管生成和上皮-间充质转化相关的基因表达谱相关。这些数据可能有助于更好地理解转移扩散的潜在靶点,并为更好地管理子宫内膜癌提供临床重要信息。