Simiantonaki Nektaria, Taxeidis Marios, Jayasinghe Caren, Kirkpatrick Charles James
Institute of Pathology, Johannes Gutenberg University, Mainz, Germany.
Anticancer Res. 2007 Sep-Oct;27(5A):3245-50.
Vascular endothelial growth factor (VEGF), originally identified as an endothelium-specific factor, can also bind to malignant cells, a mechanism by which a tumor could regulate its own progression. The biological effects of VEGF are mediated by three receptors (VEGFRs), VEGFR-1, VEGFR-2 and VEGFR-3. This study aimed at defining the expression of VEGFs in colorectal cancer (CRC) epithelia and their relationship to the metastatic status.
Using immunohistochemistry, the levels of tumoral immunoreactivity for VEGFs in 105 nonmetastatic, lymphogenously-metastatic and haematogenously-metastatic CRC specimens were assessed. Statistical analysis was performed using Fisher's exact probability test.
VEGFR-1 immunoreactivity was positive in only 50% of the cases. However lack of expression of VEGFR-1 was significantly associated with lymphogenous and haematogenous metastases. VEGFR-2 and VEGFR-3 were expressed in all investigated specimens to varying degrees. Low levels of VEGFR-2 were significantly associated with distant metastases. No significant changes were detected in VEGFR-3 expression.
Epithelial expression of VEGFR-1 and VEGFR-2 appear to have a protective effect against tumor aggressiveness in CRC.
血管内皮生长因子(VEGF)最初被鉴定为一种内皮细胞特异性因子,它也能与恶性细胞结合,这是肿瘤调节自身进展的一种机制。VEGF的生物学效应由三种受体(VEGFRs)介导,即VEGFR-1、VEGFR-2和VEGFR-3。本研究旨在确定VEGF在结直肠癌(CRC)上皮中的表达及其与转移状态的关系。
采用免疫组织化学方法,评估105例非转移性、淋巴道转移和血行转移CRC标本中VEGF的肿瘤免疫反应水平。采用Fisher精确概率检验进行统计学分析。
仅50%的病例中VEGFR-1免疫反应呈阳性。然而,VEGFR-1表达缺失与淋巴道和血行转移显著相关。VEGFR-2和VEGFR-3在所有研究标本中均有不同程度的表达。VEGFR-2低水平与远处转移显著相关。VEGFR-3表达未检测到显著变化。
VEGFR-1和VEGFR-2的上皮表达似乎对CRC的肿瘤侵袭性具有保护作用。