Lazăr Daniela, Tăban Sorina, Ardeleanu Carmen, Simionescu Cristiana, Sporea I, Cornianu Marioara, Vernic Corina
Department of Gastroenterology, Victor Babeş University of Medicine and Pharmacy, Timisoara, Romania.
Rom J Morphol Embryol. 2008;49(3):371-9.
The mechanisms by which COX-2 contributes to the carcinogenesis are not known until present. It seems that the COX-2 enzyme stimulates the cell proliferation, inhibits the apoptosis, increases the malignant cells' invasiveness and induces the angiogenesis by elaborating some angiogenic factors.
In the present study, we intend to evaluate the immunohistochemical expression of COX-2 in gastric carcinomas, keeping track of the correlations between the clinicopathologic factors, the tumor angiogenesis (evaluated by microvascular density--MVD--determination and by VEGF expression) and the patients' survival. In addition, we have tracked the immunoreactions' positivation in the peritumoral mucosa with various lesions, with the purpose to establish the contribution of COX-2 to the gastric carcinogenesis during the pre-invasive stages. A prospective study was realized, regarding the evolution and aggressiveness of the gastric cancer, with a duration of five years, 61 patients operated of gastric cancer being included.
The COX-2 immunoreactions have been significantly more frequent noticed in the gastric carcinomas included in the study (57.4%) and in the epithelial dysplasia areas adjacent to the carcinomas of intestinal type (35.5% of the cases), than in the normal peritumoral mucosa (4.9%) (p<0.001 ES). The COX-2 immunoreactions have turned positive more frequently in gastric carcinomas of intestinal type (68.4%), in comparison to the carcinomas of diffuse type (29.4%) (p<0.001 ES). The COX-2 expression is significantly correlated with the invasion level, the presence of the metastases in the regional lymph nodes and the pTNM stage, but without influencing the prognosis of the gastric cancer patients. The negative VEGF carcinomas have turned positive for COX-2 only for 19% of the cases. Different from those, the positive VEGF carcinomas have associated COX-2 immunoreactivity in 77.5% of the cases.
The results obtained are suggestive for the predominant expression of COX-2 in the carcinomas of intestinal type and its precursory lesions. Our results show a tight correlation between the immunohistochemical expressions of COX-2 and VEGF in gastric carcinomas (r = 0.562, p < 0.001 ES) and also a MVD average value significantly higher in the positive COX-2 carcinomas, suggesting an intense angiogenesis activity in that group of tumors (p < 0.001 ES).
到目前为止,COX - 2促成癌症发生的机制尚不清楚。似乎COX - 2酶通过释放一些血管生成因子来刺激细胞增殖、抑制细胞凋亡、增加恶性细胞的侵袭性并诱导血管生成。
在本研究中,我们旨在评估COX - 2在胃癌中的免疫组化表达,追踪其与临床病理因素、肿瘤血管生成(通过微血管密度——MVD——测定和VEGF表达评估)以及患者生存率之间的相关性。此外,我们追踪了不同病变的肿瘤周围黏膜中免疫反应的阳性情况,目的是确定COX - 2在癌前阶段对胃癌发生的作用。我们进行了一项关于胃癌进展和侵袭性的前瞻性研究,为期五年,纳入了61例接受胃癌手术的患者。
在本研究纳入的胃癌(57.4%)和肠型癌相邻的上皮发育异常区域(35.5%的病例)中,COX - 2免疫反应的出现频率显著高于正常肿瘤周围黏膜(4.9%)(p<0.001,效应量)。与弥漫型癌(29.4%)相比,COX - 2免疫反应在肠型胃癌中更频繁地呈阳性(68.4%)(p<0.001,效应量)。COX - 2表达与侵袭程度、区域淋巴结转移的存在及pTNM分期显著相关,但不影响胃癌患者的预后。VEGF阴性的癌中只有19%的病例COX - 2呈阳性。与之不同的是,VEGF阳性的癌中有77.5%的病例伴有COX - 2免疫反应性。
所得结果提示COX - 2在肠型癌及其前驱病变中主要表达。我们的结果显示胃癌中COX - 2和VEGF的免疫组化表达之间存在紧密相关性(r = 0.562,p < 0.001,效应量),并且COX - 2阳性的癌中MVD平均值显著更高,表明该组肿瘤中有强烈的血管生成活性(p < 0.001,效应量)。