Kaushal Varsha, Mukunyadzi Perkins, Dennis Richard A, Siegel Eric R, Johnson Donald E, Kohli Manish
Department of Internal Medicine, Division of Hematology/Oncology, University of Arkansas for Medical Sciences, 4301 West Markham, Little Rock, AR 72205, USA.
Clin Cancer Res. 2005 Jan 15;11(2 Pt 1):584-93.
The vascular endothelial growth factor (VEGF) family plays a critical role in tumor angiogenesis and lymphangiogenesis. We characterized, at the mRNA and protein levels, the expression of VEGF-A and VEGF-D and their cognate receptors, VEGFR-1, VEGFR-2, and VEGFR-3 in early- and advanced-stage prostate cancer specimens.
The levels of VEGF-A and VEGF-D mRNA in early- and advanced-stage specimens were compared using an angiogenic gene array and were confirmed by quantitative real-time PCR. Receptor protein levels and activation status were determined by immunoblotting. Spatial expression of the proteins was evaluated using immunohistochemistry with fresh and archival tissues from benign prostatic hypertrophy specimens, early-stage prostate specimens, and advanced-stage metastatic specimens. Circulating plasma levels of these growth factors were measured using ELISAs.
We observed that expression patterns of VEGF isotypes corresponded to the prostate cancer stage: high expression of angiogenic growth factor VEGF-A was observed in early-stage prostate specimens, whereas high expression of lymphangiogenic growth factor VEGF-D was associated with advanced-stage metastatic disease. All VEGF receptors were present at variable levels in all specimens, but their activation states varied in a stage-specific manner. VEGFR-1 and, to a limited extent, VEGFR-2 were activated in early-stage specimens, whereas VEGFR-2 and VEGFR-3 were activated in advanced-stage specimens.
Our results suggest that lymphangiogenic markers, such as VEGF-D and VEGFR-2 and VEGFR-3, may be better than angiogenic markers as targets of therapeutic intervention in advanced-stage prostate disease.
血管内皮生长因子(VEGF)家族在肿瘤血管生成和淋巴管生成中起关键作用。我们在mRNA和蛋白质水平上,对早期和晚期前列腺癌标本中VEGF-A和VEGF-D及其同源受体VEGFR-1、VEGFR-2和VEGFR-3的表达进行了表征。
使用血管生成基因阵列比较早期和晚期标本中VEGF-A和VEGF-D mRNA的水平,并通过定量实时PCR进行确认。通过免疫印迹法测定受体蛋白水平和激活状态。使用来自良性前列腺增生标本、早期前列腺标本和晚期转移标本的新鲜和存档组织进行免疫组织化学,评估蛋白质的空间表达。使用酶联免疫吸附测定法测量这些生长因子的循环血浆水平。
我们观察到VEGF同种型的表达模式与前列腺癌分期相对应:在早期前列腺标本中观察到血管生成生长因子VEGF-A的高表达,而淋巴管生成生长因子VEGF-D的高表达与晚期转移疾病相关。所有VEGF受体在所有标本中的水平各不相同,但其激活状态以阶段特异性方式变化。VEGFR-1以及在有限程度上VEGFR-2在早期标本中被激活,而VEGFR-2和VEGFR-3在晚期标本中被激活。
我们的结果表明,作为晚期前列腺疾病治疗干预的靶点,淋巴管生成标志物如VEGF-D、VEGFR-2和VEGFR-3可能比血管生成标志物更好。