Kolev Yanislav, Uetake Hiroyuki, Iida Satoru, Ishikawa Toshiaki, Kawano Tatsuyuki, Sugihara Kenichi
Surgical Oncology, Graduate School, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, 113-8519 Tokyo, Japan.
Ann Surg Oncol. 2007 Oct;14(10):2738-47. doi: 10.1245/s10434-007-9484-7. Epub 2007 Aug 9.
Many studies have shown that angiogenesis plays an important role in the process of cancer development and progression. Vascular endothelial growth factor (VEGF) has a potent angiogenic activity, and cyclooxygenase-2 (COX-2) supports angiogenesis by regulated production of angiogenic factors, including VEGF. The purpose of this study was to examine the expression of VEGF in combination with COX-2 and CD34, their correlation with various clinicopathological factors, and their prognostic significance in human gastric carcinoma.
Specimens from 169 patients with different grade and stage gastric carcinoma were investigated by immunohistochemistry for COX-2 and VEGF expression. Tumor microvessel density was assessed with CD34 immunostaining. Correlations between the expression of VEGF, COX-2, CD34, and various clinicopathological factors were studied. The effect of these proteins on patient survival was determined.
COX-2 and VEGF were positively expressed in 36.7% and 50.3% of the patients, respectively. Positive correlation was found between VEGF and COX-2 and between VEGF and CD34. VEGF expression was correlated with depth of invasion; metastatic lymph nodes; lymphatic and venous invasion; and tumor, node, metastasis system stage. Patients with positive staining for VEGF showed far lower disease-free (64.9% vs. 81.3%) and overall (58.3% vs. 76.9%) survival rates than VEGF-negative patients. In multivariate analysis, only tumor location, depth of invasion, and lymph node metastasis were shown to be independent prognostic factors.
VEGF expression correlates with angiogenesis and tumor progression and is a valuable prognostic factor in patients with gastric carcinoma.
许多研究表明,血管生成在癌症发生和发展过程中起重要作用。血管内皮生长因子(VEGF)具有强大的血管生成活性,而环氧合酶-2(COX-2)通过调节包括VEGF在内的血管生成因子的产生来支持血管生成。本研究的目的是检测VEGF与COX-2和CD34的联合表达、它们与各种临床病理因素的相关性以及它们在人类胃癌中的预后意义。
采用免疫组织化学法检测169例不同分级和分期胃癌患者标本中COX-2和VEGF的表达。用CD34免疫染色评估肿瘤微血管密度。研究VEGF、COX-2、CD34的表达与各种临床病理因素之间的相关性。确定这些蛋白对患者生存的影响。
COX-2和VEGF在患者中的阳性表达率分别为36.7%和50.3%。VEGF与COX-2之间以及VEGF与CD34之间呈正相关。VEGF表达与浸润深度、转移淋巴结、淋巴管和静脉侵犯以及肿瘤、淋巴结、转移分期系统相关。VEGF染色阳性的患者无病生存率(64.9%对81.3%)和总生存率(58.3%对76.9%)远低于VEGF阴性患者。多因素分析显示,只有肿瘤部位、浸润深度和淋巴结转移是独立的预后因素。
VEGF表达与血管生成和肿瘤进展相关,是胃癌患者有价值的预后因素。