Giatromanolaki Alexandra, Sivridis Efthimios, Simopoulos Constantinos, Polychronidis Alexandros, Gatter Kevin C, Harris Adrian L, Koukourakis Michael I
Tumour and Angiogenesis Research Group, Department of Radiotherapy/Oncology, Democritus University of Thrace, Alexandroupolis, Greece.
Clin Exp Metastasis. 2002;19(8):673-9. doi: 10.1023/a:1021354028685.
Recent reports provide evidence that some growth factors behave as inhibitors of the apoptosis of the endothelial cells, bringing forward the concept of vascular survival as a post-angiogenesis process. At least two different vasculature development processes occur within a tumor: the angiogenic (formation of new vessels) and the vascular survival pathway, which is devoted to the preservation of the newly-formed vessels in layers that lose contact with the adjacent normal tissue. We developed a method to assess these processes in tissue samples. We noted that differences among tumors may exist not only in the tumor angiogenic activity (TAA) but also in the vascular survival ability (VSA). One third of the highly angiogenic breast cancer cases examined had a poor ability to maintain high vessel density in inner tumor areas. Both parameters are independently related to prognosis, while VSA was directly related to tumor dimensions and node involvement. Patients with high TAA and VSA had a particularly poor prognosis. It is suggested that although cancer angiogenic activity is important for the local invasion and dissemination into vessels and lymphatics, the VSA may be important for the effective formation of viable tumor foci in lymph nodes or distant organs. Recognition and quantification of the vascular survival ability in human tumors may significantly improve the prognostic value of the assessment of tumor vasculature, and may help to stratify patients for clinical trials with novel anti-angiogenic or angiotoxic drugs. Elucidation of the pathways may provide additional targets for antiangiogenic therapy.
近期报告提供了证据,表明一些生长因子可作为内皮细胞凋亡的抑制剂,从而提出了血管存活这一血管生成后过程的概念。肿瘤内至少发生两种不同的血管发育过程:血管生成(新血管形成)和血管存活途径,后者致力于维持与相邻正常组织失去联系的各层中新形成血管的存活。我们开发了一种方法来评估组织样本中的这些过程。我们注意到,肿瘤之间的差异可能不仅存在于肿瘤血管生成活性(TAA)中,也存在于血管存活能力(VSA)中。在检查的高血管生成性乳腺癌病例中,三分之一在肿瘤内部区域维持高血管密度的能力较差。这两个参数均独立与预后相关,而VSA与肿瘤大小和淋巴结受累直接相关。TAA和VSA高的患者预后特别差。有人提出,尽管癌症血管生成活性对于局部侵袭以及向血管和淋巴管的扩散很重要,但VSA对于在淋巴结或远处器官中有效形成存活肿瘤病灶可能很重要。识别和量化人类肿瘤中的血管存活能力可能会显著提高肿瘤血管评估的预后价值,并可能有助于对患者进行分层,以便进行新型抗血管生成或血管毒性药物的临床试验。阐明这些途径可能会为抗血管生成治疗提供更多靶点。