Tabriz Hedieh Moradi, Mirzaalizadeh Marzieh, Gooran Shahram, Niki Farzaneh, Jabri Maryam
Pathology, Sina Hospital, Tehran University of Medical Sciences, Tehran, Iran E-mail :
Asian Pac J Cancer Prev. 2016;17(2):535-8. doi: 10.7314/apjcp.2016.17.2.535.
Cyclooxygenase 2 (COX-2) is important as an enzyme in the pathway leading to the production of prostaglandin E2 (PGE2) and arachidonic acid. This pathway is known to play a role in inflammation, tumor growth, invasiveness and metastasis, inhibition of apoptosis and angiogenesis. Inhibition of COX-2 has been shown to be a promising antitumor and antiangiogenic strategy in several tumor types, including renal cell carcinoma (RCC). Therefore, we decided to evaluate the immunohistochemical expression of this marker and its association with several clinicopathological characteristics in a series of cases.
COX-2 expression was examined immunohistochemically in tumor tissues obtained from 96 patients who underwent radical (94 cases) or partial (2 cases) nephrectomy. Correlations between COX-2 expression and clinicopathologic findings including pathologic stage, nuclear grade and other indicator of prognosis were examined.
Of 96 tumors, 20.9% were positive for COX-2 expression. A correlation was found between COX-2 expression and tumor histological subtype (P=0.03).The papillary subtype showed maximum expression of this marker (43.8%) and the clear subtype minimum (14.7%). There were also possible links between COX-2 expression and pathologic stage, nuclear grade and nodal involvement but the results were not statistically significant (P=0.8, P= 0.14 and P=0.06, respectively). No correlation was found between COX2 expression and patient age, gender, tumor size, metastasis or survival.
In our study, COX-2 expression was correlated with the histological subtype of RCC. Additional research is required to determine the link between COX-2 expression and prognosis and also evaluation of probable effectiveness of COX-2 inhibitor drugs in treatment of RCC patients.
环氧化酶2(COX-2)作为一种酶,在前列腺素E2(PGE2)和花生四烯酸的生成途径中起着重要作用。已知该途径在炎症、肿瘤生长、侵袭和转移、细胞凋亡抑制及血管生成中发挥作用。在包括肾细胞癌(RCC)在内的几种肿瘤类型中,抑制COX-2已被证明是一种有前景的抗肿瘤和抗血管生成策略。因此,我们决定在一系列病例中评估该标志物的免疫组化表达及其与几种临床病理特征的相关性。
对96例行根治性肾切除术(94例)或部分肾切除术(2例)患者的肿瘤组织进行COX-2表达的免疫组化检测。检测COX-2表达与包括病理分期、核分级及其他预后指标在内的临床病理结果之间的相关性。
96例肿瘤中,20.9%的COX-2表达呈阳性。发现COX-2表达与肿瘤组织学亚型之间存在相关性(P=0.03)。乳头状亚型该标志物的表达最高(43.8%),透明细胞亚型最低(14.7%)。COX-2表达与病理分期、核分级及淋巴结受累之间也可能存在联系,但结果无统计学意义(分别为P=0.8、P=0.14和P=0.06)。未发现COX-2表达与患者年龄、性别、肿瘤大小、转移或生存之间存在相关性。
在我们的研究中,COX-2表达与RCC的组织学亚型相关。需要进一步研究以确定COX-2表达与预后之间的联系,并评估COX-2抑制剂药物治疗RCC患者的可能疗效。