Expressions of MMP2, TIMP2, Ki-67 and P53 in glioma tissues and their significance

Xuejuan Yu, H. An, Yamei Sun, Zheng Jiang, Xuehai Zhang, Wenjing Yang, Wei Zhang
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Abstract

Objective To investigate the expressions and significance of matrix metalloproteinase 2 (MMP2), tissue inhibitor of metalloproteinase 2 (TIMP2), Ki-67 and P53 in human glioma tissues. Methods The expressions of Ki-67 and P53 in paraffin samples of 50 gliomas (immunohistochemistry SP method) from January 1995 to December 2015 in Qilu Hospital of Shandong University were analyzed retrospectively, and the expressions of MMP2 and TIMP2 were detected by immunohistochemistry. The differences of parameters between high- and low-grade gliomas were compared by χ2 test and their correlations were assessed by Spearman correlation analysis. Results In the high-grade group (grade Ⅲ-Ⅳ, n=37), the high expression rate of MMP2 was 81.08% (30/37), the positive expression rates of Ki-67 and P53 were 78.38% (29/37) and 72.97% (27/37). In the low-grade group (grade Ⅰ-Ⅱ, n=13), there were 2 patients with high expression of MMP2, 3 patients with positive expression of Ki-67 and P53 respectively, and there were significant differences between the two groups (χ2=15.282, P<0.001; χ2=10.482, P=0.001; χ2=9.979, P=0.002). A significant correlation was found between them and pathological grade (r=0.600, P<0.001; r=0.505, P<0.001; r=0.447, P=0.001). The high expression of TIMP2 was found in 8 cases of low-grade group and 19 cases (51.35%) of high-grade group, with no significant difference (χ2=0.402, P=0.526). The expression of MMP2 was positively correlated with Ki-67 and P53 (r=0.392, P=0.005; r=0.323, P=0.022), while TIMP2 was negatively correlated with Ki-67 (r=-0.441, P=0.001). The expression of P53 was positively correlated with Ki-67 (r=0.748, P<0.001). Conclusion MMP2, Ki-67 and P53 may play important role in the proliferation and invasiveness of glioma. The mechanism of TIMP2 is complicated and needs further study. Key words: Glioma; Matrix metalloproteinase 2; Tissue inhibitor of metalloproteinase 2; Ki-67 antigen; Tumor suppressor protein P53
MMP2、TIMP2、Ki-67、P53在胶质瘤组织中的表达及意义
目的探讨基质金属蛋白酶2 (MMP2)、组织金属蛋白酶2抑制剂(TIMP2)、Ki-67和P53在人脑胶质瘤组织中的表达及意义。方法回顾性分析1995年1月至2015年12月山东大学齐鲁医院50例胶质瘤石蜡标本(免疫组织化学SP法)中Ki-67、P53的表达情况,免疫组织化学检测MMP2、TIMP2的表达情况。采用χ2检验比较高分级与低分级胶质瘤间各参数的差异,采用Spearman相关分析比较其相关性。结果高级别组(分级Ⅲ~Ⅳ,n=37) MMP2高表达率为81.08% (30/37),Ki-67和P53阳性表达率分别为78.38%(29/37)和72.97%(27/37)。低分级(Ⅰ~Ⅱ,n=13)组MMP2高表达2例,Ki-67、P53阳性表达3例,两组间差异有统计学意义(χ2=15.282, P<0.001;χ2 = 10.482,P = 0.001;χ2 = 9.979,P = 0.002)。与病理分级有显著相关性(r=0.600, P<0.001;r = 0.505, P < 0.001;r = 0.447, P = 0.001)。TIMP2高表达在低分级组8例,高分级组19例(51.35%),差异无统计学意义(χ2=0.402, P=0.526)。MMP2的表达与Ki-67、P53呈正相关(r=0.392, P=0.005;r=0.323, P=0.022), TIMP2与Ki-67呈负相关(r=-0.441, P=0.001)。P53的表达与Ki-67呈正相关(r=0.748, P<0.001)。结论MMP2、Ki-67和P53可能在胶质瘤的增殖和侵袭过程中起重要作用。TIMP2的作用机制较为复杂,有待进一步研究。关键词:胶质瘤;基质金属蛋白酶2;金属蛋白酶2组织抑制剂;ki - 67抗原;肿瘤抑制蛋白P53
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