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环氧化酶-2表达与卵巢癌血管生成的临床意义

Clinical implications of expression of cyclooxygenase-2 related to angiogenesis in ovarian cancer.

作者信息

Fujimoto Jiro, Toyoki Hiroshi, Sakaguchi Hideki, Jahan Israt, Alam Syed Mahfuzul, Tamaya Teruhiko

机构信息

Department of Obstetrics and Gynecology, Gifu University School of Medicine, Japan.

出版信息

Oncol Rep. 2006 Jan;15(1):21-5.

Abstract

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.

摘要

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。

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