Fujimoto Jiro, Toyoki Hiroshi, Sakaguchi Hideki, Jahan Israt, Alam Syed Mahfuzul, Tamaya Teruhiko
Department of Obstetrics and Gynecology, Gifu University School of Medicine, Japan.
Oncol Rep. 2006 Jan;15(1):21-5.
Angiogenesis is essential for the development, growth and advancement of solid tumors. Cyclooxygenase (cox)-2 is recognized as an angiogenic factor in various tumors. This prompted us to study the clinical implications of cox-2 expression and angiogenesis in ovarian cancer. There was a significant correlation between microvessel counts and cox-2 levels. Cox-2 localized in the cancer cells, but not in the stromal cells of ovarian cancer tissue. Cox-2 levels increased with the advancement, and the prognosis of the 30 patients with high cox-2 expression was extremely poor (33%), while the 24-month survival rate of the other 30 patients, those with low cox-2 expression, was 67%. Furthermore, cox-2 levels significantly correlated with VEGF levels. VEGF associated with cox-2 might work on angiogenesis with advancement. Therefore, long-term administration of cox-2 inhibitors might be effective on the suppression of regrowth or recurrence after intensive treatment for advanced ovarian cancer.
血管生成对于实体瘤的发生、生长和进展至关重要。环氧合酶(COX)-2被认为是多种肿瘤中的血管生成因子。这促使我们研究COX-2表达和血管生成在卵巢癌中的临床意义。微血管计数与COX-2水平之间存在显著相关性。COX-2定位于癌细胞中,而非卵巢癌组织的基质细胞中。COX-2水平随病情进展而升高,30例COX-2高表达患者的预后极差(33%),而另外30例COX-2低表达患者的24个月生存率为67%。此外,COX-2水平与VEGF水平显著相关。与COX-2相关的VEGF可能随着病情进展作用于血管生成。因此,长期给予COX-2抑制剂可能对晚期卵巢癌强化治疗后的再生长或复发抑制有效。