Kahn Benjamin M, Lucas Alfredo, Alur Rohan G, Wengyn Maximillian D, Schwartz Gregory W, Li Jinyang, Sun Kathryn, Maurer H Carlo, Olive Kenneth P, Faryabi Robert B, Stanger Ben Z
Department of Medicine.
Department of Cell and Developmental Biology.
J Clin Invest. 2021 Jan 19;131(2). doi: 10.1172/JCI136655.
Tumors depend on a blood supply to deliver oxygen and nutrients, making tumor vasculature an attractive anticancer target. However, only a fraction of patients with cancer benefit from angiogenesis inhibitors. Whether antiangiogenic therapy would be more effective if targeted to individuals with specific tumor characteristics is unknown. To better characterize the tumor vascular environment both within and between cancer types, we developed a standardized metric - the endothelial index (EI) - to estimate vascular density in over 10,000 human tumors, corresponding to 31 solid tumor types, from transcriptome data. We then used this index to compare hyper- and hypovascular tumors, enabling the classification of human tumors into 6 vascular microenvironment signatures (VMSs) based on the expression of a panel of 24 vascular "hub" genes. The EI and VMS correlated with known tumor vascular features and were independently associated with prognosis in certain cancer types. Retrospective testing of clinical trial data identified VMS2 classification as a powerful biomarker for response to bevacizumab. Thus, we believe our studies provide an unbiased picture of human tumor vasculature that may enable more precise deployment of antiangiogenesis therapy.
肿瘤依赖血液供应来输送氧气和营养物质,这使得肿瘤血管系统成为一个有吸引力的抗癌靶点。然而,只有一小部分癌症患者能从血管生成抑制剂中获益。针对具有特定肿瘤特征的个体进行抗血管生成治疗是否会更有效尚不清楚。为了更好地描述不同癌症类型内部和之间的肿瘤血管环境,我们开发了一种标准化指标——内皮指数(EI),用于从转录组数据估算超过10000例人类肿瘤(对应31种实体瘤类型)中的血管密度。然后,我们使用该指数比较高血管化和低血管化肿瘤,从而能够根据一组24个血管“枢纽”基因的表达情况将人类肿瘤分为6种血管微环境特征(VMS)。EI和VMS与已知的肿瘤血管特征相关,并且在某些癌症类型中与预后独立相关。对临床试验数据的回顾性测试确定VMS2分类是对贝伐单抗反应的有力生物标志物。因此,我们相信我们的研究提供了一幅关于人类肿瘤血管系统的客观图景,这可能使抗血管生成治疗的部署更加精确。