卵巢癌中PGRMC1基因表达与微血管密度的关系

Expression of PGRMC1 and Its Relationship with MVD in Ovarian Cancer

  • 摘要:
      目的  检测人卵巢癌组织中PGRMC1(progesterone receptor membrane component-1)基因表达情况,探讨PGRMC1基因在卵巢癌发生发展过程中的作用。
      方法  利用免疫组织化学方法检测78例不同病变卵巢组织蜡块中PGRMC1基因及蛋白表达情况;以TBP(TATA box binding protein)为内源性对照基因,利用实时定量PCR方法检测了10例正常新鲜卵巢组织和30例新鲜卵巢癌组织中PGRMC1基因的mRNA表达水平。
      结果  采用免疫染色强度加着色面积的积分标准判断免疫组织化学结果,与正常卵巢(0.20±0.71)及卵巢良性肿瘤组(0.75±1.12)相比,卵巢交界性肿瘤中PGRMC1蛋白表达(3.60±1.14)和卵巢癌(7.30±2.12)显著增高(P < 0.01)。实时定量PCR方法证实卵巢癌组PGRMC1 mRNA表达(3.526±1.386)显著高于良性卵巢病变组(0.936±0.725)(P < 0.01),是良性卵巢病变组织表达的3.51倍。PGRMC1蛋白阳性表达的卵巢组织中,正常卵巢组MVD为(18.6±6.7)条;良性卵巢病变组MVD为(20.9±7.9)条;交界性卵巢肿瘤组MVD为(22.4±4.7)条;卵巢癌组MVD为(28.4±8.1)条,卵巢癌组与正常卵巢组、良性卵巢肿瘤组间差异有统计学意义(P < 0.01)。
      结论  PGRMC1高表达可能与卵巢癌的发生、发展有关,并可能促进血管生成。

     

    Abstract:
      Objective  To examine the expression of progesterone receptor membrane component-1 (PGRMC1) gene and explore its effect on the evolution of ovarian cancers.
      Methods  The protein expression of PGRMC1 in various ovarian lesions was detected by immunohistochemistry. TATA box binding protein gene was used as an endogenous control. The mRNA expression of PGRMC1 gene in 10 cases of benign ovarian tumor tissues and 30 cases of epithelial ovarian cancer tissue was quantified by real-time PCR.
      Results  The expression levels of PGRMC1 protein in borderline ovarian tumor (3.60 ± 1.14) and ovarian cancer (7.30 ± 2.12) tissues were significantly higher than in normal ovarian (0.20 ± 0.71) and benign ovarian tumor (0.75 ± 1.12) tissues (all P < 0.01). Real-time PCR confirmed that the mRNA expression level was significantly different between ovarian cancer (3.526 ± 1.386) and benign ovarian tumor (0.936 ± 0.725) tissues (P < 0.01). The microvessel density in ovarian cancer tissues (28.4 ± 8.1) was significantly higher than in normal ovarian (18.6 ± 6.7) and benign ovarian tumor (20.9 ±7.9) tissues (all P < 0.01).
      Conclusion  The expression of PGRMC1 gene in ovarian tumor tissues is significantly elevated, which may play an important role in the occurrence, development, and angiogenesis of ovarian cancer.

     

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