角蛋白7在卵巢上皮性肿瘤中的表达水平及良性卵巢上皮性肿瘤的恶性转移。

Minghui Lin, Jinhua Wang, Shaoyu Wang, Yuxiu Huang
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引用次数: 1

摘要

探讨角蛋白7 (keratin 7, KRT7)在卵巢上皮性肿瘤恶性转移和卵巢良性上皮性肿瘤中的诊断价值。2018年1月至2019年1月,在福建医科大学第一附属医院采集卵巢良性上皮性肿瘤新鲜组织30例、交界性肿瘤新鲜组织30例、转移性卵巢新鲜组织30例,正常卵巢组织新鲜组织30例作为对照组。FIGO分期标准:ⅰ期25例,ⅱ期26例,ⅲ期16例,ⅳ期23例。采用实时荧光定量PCR检测KRT7的相对表达,分析KRT7表达与上皮性卵巢癌分级的关系。结果显示,KRT7在卵巢正常组织中阳性表达率为12.1%,在卵巢良性上皮性肿瘤中阳性表达率为28.4%,在交界性肿瘤中阳性表达率为53.5%,在转移性卵巢癌中阳性表达率为24.2%。随着肿瘤分期的增加,KRT7的相对表达量显著降低,但ⅰ期与ⅱ期、ⅲ期与ⅳ期之间差异无统计学意义(P > 0.05)。I期与III期、IV期比较差异有统计学意义(P < 0.05)。上皮性卵巢癌患者与对照组比较差异有统计学意义(P < 0.05)。综上所述,与对照组相比,KRT7在卵巢良性上皮性肿瘤和交界性肿瘤患者中的表达均显著降低。KRT7在卵巢良性上皮性肿瘤中的表达水平低于交界性肿瘤。KRT7的表达与卵巢癌的发生、发展、恶化有关,为肿瘤的靶向治疗提供了依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expression Level of Keratin 7 in Epithelial Ovarian Cancer and Malignant Metastasis of Benign Epithelial Ovarian Tumors.

It was to investigate the diagnostic value of keratin 7 (KRT7) in malignant metastasis of epithelial ovarian cancer and benign epithelial ovarian tumors. From January 2018 to January 2019, 30 fresh tissues of benign epithelial ovarian tumors, 30 fresh tissues of borderline tumors, 30 fresh tissues of metastatic ovarian were collected in The First Affiliated Hospital of Fujian Medical University, and 30 fresh tissues of normal ovarian tissues were collected as the control group. Federation of gynecology and obstetrics (FIGO) staging criteria: 25 cases of stage I, 26 cases of stage II, 16 cases of stage III, and 23 cases of stage IV. The relative expression of KRT7 was detected by real-time fluorescence quantitative PCR, and the relationship between KRT7 expression and epithelial ovarian cancer grading was analyzed. The results showed that the positive expression rate of KRT7 was 12.1% in normal ovarian tissues, 28.4% in benign epithelial ovarian tumors, 53.5% in borderline tumors, and 24.2% in metastatic ovarian cancer. With the increase of tumor stage malignancy, the relative expression of KRT7 decreased significantly, but there was no significant difference between stage I and stage II, stage III and stage IV (P > 0.05). The difference between stage I and stage III, and stage IV was significant (P < 0.05). Patients with epithelial ovarian cancer had a significant difference compared with the control group (P < 0.05). In summary, compared with the control group, the expression of KRT7 in patients with benign epithelial ovarian tumors and borderline tumors was significantly decreased. The expression level of KRT7 in benign epithelial ovarian tumors was lower than that in borderline tumors. The expression of KRT7 was related to the occurrence, development, and deterioration of ovarian cancer, which provided a basis for targeted therapy of tumors.

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