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PTEN 、MMP27 、VEGF 在骨巨细胞瘤中的表达

Expressions of PTENand MMP-7 、VEGF in Giant Cell Tumor of Bone ( GCT)

  • 摘要: 目的 探讨骨巨细胞瘤中的PTEN、MMP-7、VEGF表达与“三结合分类”、病理分级及复发、转移的关系。方法 采用免疫组化法检测65例骨巨细胞瘤标本盯EN、MMP-7、VEGF基因蛋白的表达,分析其与骨巨细胞瘤临床病理分期、分级及复发、转移的关系。结果 PTEN、MMP-7、VEGF的阳性表达率分别为56.95%、72.30%、49.20%;在“三结合分类”组中PTEN的阳性表达率分别为83.3%、68.10%、28.00%,呈下降趋势,良性与中间性组间差异不显著(P=0.271),而中间性与恶性组间差异明显(P=0.001);而MMP-7阳性表达率分别为39.00%、72.50%、96.00%,VEGF阳性表达率分别为16.67%、54.50%、68.00%,组间差异明显(P=0.031、0.001);在转移组中PTEN、MMP-7、VEGF的阳性表达率分别为30.00%、100%、85.00%,在无转移组中PTEN、MMP-7、VEGF的阳性表达率分别为68.80%、60.00%、33.3%,两组间差异明显(P=0.003、0.001、0.001);复发组中PTEN、MMP-7、VEGF的阳性表达率分别为33.30%、93.30%、86.60%,无复发组中PTEN、MMP-7、VEGF的阳性表达率分别为64.00%、66.00%、38.00%,两组间差异明显(P=0.035、0.038、0.001),且PTEN与MMP-7、VEGF负相关(P=0.001、0.020),而与病理分级及年龄、性别无统计学差异。结论 PTEN、MMP-7、VEGF的表达与“三结合分类”有一定的关系,并与转移、复发显著相关,联合检测有助于骨巨细胞瘤的临床评估,对其预后判断具有重要临床意义。

     

    Abstract: Objective  To evaluate the expressions of PTEN ( phosphatase and tension homologue deleted on chromosome 10), MMP-7 (matrix metalloproteinases-7, MMP-7), VEGF (vascular endothelial growth factor) and their relationships with clinical factors, pathological types and metastasis, recurrence of giant cell tumor of bone ( GCT) . Methods  The expressions of PTEN, MMP-7, VEGF in 65 cases of human GCT were detected by using immunohistochemical staining. The expressions of PTEN, MMP-7, VEGF and other clinical fractures were analyzed with the metastasis and recurrence of the tumor. Results  The expressions of the PTEN, MMP-7, VEGF in GCT were 56. 95 % and 72. 30 %, 49. 20 %, respectively. In the clinical-pathological-X-ray groups, the expressions of PTEN were 83. 30 %, 68. 10 %, 28. 00 %, the positive rate had no significantly difference between the Non2malignant and doutful-malignant groups, P> 0. 05 ( P = 0. 271), but there were significantly difference between the doutful-malignant and malignant groups, P < 0. 05 ( P = 0. 001) ; the expression of MMP-7 were 39. 00 %, 72. 50 %, 96. 00 %, and the expression of VEGF were 16. 67 %, 54. 50 %, 68. 00 %, the positive rates of them had significantly difference, P < 0. 05 ( P = 0. 031, 0. 001) ; the expressions of PTEN, MMP-7, VEGF in the recurrence group were 33. 30 %, 93. 30 %, 86. 60 %, but in the nonrecurrence group were 64. 00 %, 66. 00 %, 38. 00 %, their expressions were statistically related to the recurrence of GCT, P < 0. 05 ( P = 0. 035, 0. 038, 0. 001) ; in the metastasis group, the expressions of PTEN, MMP-7, VEGF were 30. 00 %, 100 %, 85. 00 %, in the no metastasis group, the positive rates of PTEN, MMP-7, VEGF were 68. 80 %, 60. 00 %, 33. 30 %, the positive rates of them had significantly difference, P < 0. 05 ( P = 0. 003, 0. 001, 0. 001) ;at the same time, The expression of PTEN in GCT was inversely correlated with the expressions of VEGF and MMP-7, P <0. 05 ( P = 0. 001, 0. 02) ; However, the expressions of PTEN 、MMP-7 、VEGF had no statistically significance with the pathological types and sexuality. Conclusion  The decreased expression of PTEN and increased expressions of MMP-7 、VEGF have significant relationship to the prognosis of GCT. The combined detection of PTEN and MMP-7 may be of important clinical value to evaluate the infilt rative ability and prognosis of GCT.

     

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