Sanaat Zohreh, Tavangar Seyed-Mohammad, Gharamaleki Jalil Vaez, Kermani Iraj Aswadi, Ziae Jamal Eivazi, Nikanfar Alireza, Esfahani Ali, Chavoshi Seyyed Hadi, Bevrani H, Akbari Farideh
Associate professor of hematology-oncology, Hematology-oncology Research Center, Tabriz University of Medical Science, Tabriz, Iran.
Professor of pathology, pathology department, shariati hospital, Tehran University of Medical Science, Tehran, Iran.
Int J Hematol Oncol Stem Cell Res. 2013;7(1):1-4.
Lymphomas are a group of malignancies affecting B, T and NK cells. Cyclooxygenase-2 (COX-2) enzyme is one of the known inflammatory factors which increase during the inflammation process. Increase in COX-2 expression inhibits apoptosis and increases tumor cells invasion and angiogenesis. Increase in the COX-2 gene expression is seen in a group of cancers. Specific COX-2 inhibition also can be beneficial in some cancers through apoptosis stimulation.
MATERIALS & METHODS: In this descriptive-analytic study, the degree of COX-2 expression was evaluated in patients with non-Hodgkin lymphoma. The following variables were used in this study: gender, age, lymphoma type, the stage of disease, the degree of disease, the existence of B symptom, extranodal involvement, response to treatment, death and LDH levels. Paraffin-embedded tissue blocks from 153 cases of non-Hodgkin' and Hodgkin' lymphoma were selected for immunohistochemical staining of COX-2 expression.
COX-2 level was reported positive in 4 (4.7%) patients with non-Hodgkin's lymphoma and 4 (5.7%) with Hodgkin's lymphoma. Fifteen patients experienced relapses and 9 died during the median follow-up of 7 years. There was no significant relationship between quantitative and qualitative variables and COX-2 expression. Also, there was no relationship between COX-2 and type of lymphoma (P=0.476).
According to our results, no relationship between COX-2 expression and type of lymphoma was found. We recommend more patient involvement to assess COX-2 expression. Apparently, it seems that the patient's race (Azari) may have an impact on the results of this study.
淋巴瘤是一组影响B细胞、T细胞和NK细胞的恶性肿瘤。环氧化酶-2(COX-2)是已知的炎症因子之一,在炎症过程中会增加。COX-2表达的增加会抑制细胞凋亡,并增加肿瘤细胞的侵袭和血管生成。在一组癌症中可见COX-2基因表达增加。特异性COX-2抑制通过刺激细胞凋亡在某些癌症中也可能有益。
在这项描述性分析研究中,评估了非霍奇金淋巴瘤患者COX-2的表达程度。本研究使用了以下变量:性别、年龄、淋巴瘤类型、疾病分期、疾病程度、B症状的存在、结外受累情况、治疗反应、死亡情况和乳酸脱氢酶水平。选择153例非霍奇金淋巴瘤和霍奇金淋巴瘤患者的石蜡包埋组织块进行COX-2表达的免疫组化染色。
在4例(4.7%)非霍奇金淋巴瘤患者和4例(5.7%)霍奇金淋巴瘤患者中,COX-2水平呈阳性。在7年的中位随访期内,15例患者复发,9例死亡。定量和定性变量与COX-2表达之间无显著关系。此外,COX-2与淋巴瘤类型之间也无关系(P=0.476)。
根据我们的结果,未发现COX-2表达与淋巴瘤类型之间存在关系。我们建议纳入更多患者以评估COX-2表达。显然,患者的种族(阿扎里族)似乎可能对本研究结果有影响。