血栓反应蛋白-1、血管生成相关标志物和细胞外基质成分与结直肠癌预后的关系

A. Mitselou, D. Arvanitis, Urania Skoufi, D. Tsironis, E. Lampri, Ioannis Nesseris, T. Vougiouklakis, E. Briassoulis, E. Ioachim
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引用次数: 1

摘要

背景:血管生成是一个多步骤的过程,它依赖于促血管生成因子和抑制因子的平衡以及与细胞外基质的相互作用。血小板反应蛋白-1 (thrombospontin -1, TSP-1)是由THBS1基因编码的内源性血管生成抑制剂,其启动子由p53激活。目的:探讨TSP-1在结直肠癌患者中的相关性。材料与方法:我们检测了97例结直肠癌(CRC)患者血管生成药物(VEGF和CD34)、增殖相关指标、细胞外基质成分(tenascin、纤连蛋白、层粘连蛋白、IV型胶原)和抗血管生成药物TPS-1的免疫组化表达,并将其表达水平与临床病理参数进行了相关性分析。结果:肿瘤细胞、间质及血管周围组织中均检测到TSP-1。肿瘤TSP-1高、中表达占24.75%,低表达占19.6%,阴性占55.7%。间质高表达占40.2%,血管周围染色占31.95%。基质TSP-1表达与肿瘤类型、肿瘤分级相关(p=0.001、p=0.041),与ECM成分tenascin (p=0.053)、纤连蛋白(p=0.063)、IV型胶原(p=0.004)、层粘连蛋白(p=0.0001)表达相关。TSP-1表达与肿瘤血管生成、生长分数、p53蛋白表达及总生存率的关系无统计学意义。结论:我们的数据表明,肿瘤和间质TSP-1的表达可能不是直接的抗血管生成因子,尽管它似乎通过与其他细胞外基质成分的相互作用与结直肠癌组织的重塑有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association Between Thrombospondin-1, Angiogenesis Related Markers,and Extracellular Matrix Components with Colorectal Cancer Outcome
Background: Angiogenesis is a multistep process that depends on the balance of proangiogenic factors and in- hibitors as well as on interactions with the extracellular matrix. Thrombospondin-1 (TSP-1) is an endogenous inhibitor of angiogenesis encoded by THBS1 gene, whose promoter is activated by p53. Aim: To evaluate the relevance of TSP-1 in patients with colorectal cancer. Material and Methods: We examined the immunohistochemical expression of angiogenic agents (VEGF and CD34), pro- liferation associated indices, extracellular matrix components (tenascin, fibronectin, laminin, and collagen type IV), and the antiangiogenic agent TPS-1 in 97 patients with colorectal carcinoma (CRC) and correlated their expression levels with clinicopathological parameters. Results: TSP-1 was detected in the tumor cells, stroma and perivascular tissue. High and moderate tumor TSP-1 expres- sion was observed in 24.75%, weak in 19.6%, while 55.7% of the cases were negative. High stromal expression was ob- served in 40.2% and perivascular stain was noted in 31.95% of the cases. Stromal TSP-1 expression was correlated with tumor type and tumor grade (p=0.001, and p=0.041 respectively) and with ECM components expression: tenascin (p=0.053), fibronectin (p=0.063), collagen type IV (p=0.004) and laminin (p=0.0001). The relationship of TSP-1 expres- sion with tumor angiogenesis, growth fraction, p53 protein expression, and overall survival was not significant. Conclusions: Our data suggest that both tumor and stromal TSP-1 expression may not be a direct antiangiogenic factor, although it seems to be implicated in the remodeling of colorectal cancer tissue through interaction with other extracellu- lar matrix components.
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