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作 者:李思琦[1,2] 董颖[1] 毕蕙[1] 张晓明[1] 陈锐[1]
机构地区:[1]北京大学第一医院,北京100034 [2]北京积水潭医院,北京100035
出 处:《实用妇产科杂志》2014年第4期263-265,共3页Journal of Practical Obstetrics and Gynecology
摘 要:目的:探讨年轻妇女宫颈上皮内瘤变(CIN)Ⅰ~Ⅱ级组织中细胞周期抑制因子p16InK4a蛋白及细胞增殖活性相关抗体Ki67的表达及与病变级别的相关性。方法:选取2010年在北京大学第一医院妇产科门诊就诊、年龄小于35岁,经阴道镜活检病理诊断为CINⅠ及CINⅡ级的病例56例,对其阴道活检组织及宫颈环形电切除术(LEEP)后组织之石蜡切片,进行p16InK4a及Ki67免疫组织化学染色检测其表达。结果:①阴道镜宫颈活检组织的CINⅠ及CINⅡ中p16InK4a阳性表达率分别为30.0%、80.6%,Ki67阳性表达率分别为20.0%,77.8%,CINⅡ级病变组织中p16InK4a及Ki67阳性表达率高于CINⅠ级,差异有统计学意义(P<0.001)。②阴道镜宫颈活检组织标本及LEEP组织标本不同级别CIN病变组织中,p16InK4a及Ki67的阳性表达率存在差异(均P<0.001);p16InK4a及Ki67的阳性表达率与病变级别呈正相关(r=0.644,r=0.645)。结论:p16InK4a及Ki67在年轻妇女CINⅠ~Ⅱ级组织中均有表达,且p16InK4a及Ki67阳性表达与CIN级别相关,可在CIN病理分级中提供参考。Objective:To detect the expressios of p16^InK4a and ki67 in ClN I- Ⅱ in young women and to analyze the relations between their expressions and the grade of the CIN, Methods:56 women (≤〈35 y) with a histologic diagnosis of CIN I - Ⅱ, who attended a colposcopy with cone biopsy in Peking University First Hospital Obstetrics and Gynecology out-patient department in 2010, were included in this study. p16 ^InK4a and ki67 Immunohistochemical staining were performed on all tissues to detect their expressions. Re- sults:①ln punch biopsy tissues: positive expression rate of p16^InK4a in CIN I and CIN Ⅱ were 30. 0% and 80.6%, respectively; positive expression rate of Ki67 in CIN I and CIN Ⅱ were 20.0% ,77. 8%, respective- ly,the positive expression rates of p16^InK4a and Ki67 in CIN Ⅱ were significantly higher than those of CIN [ ( P 〈0. 001 ). ②ln punch biopsy tissues and LEEP tissues: there were significant differences in positive ex- pression rate of p16 ^InK4a and ki67 among different grade of CIN( P 〈0. 001 ), both p16^InK4a and ki67 expres- sion and lesion of CIN have a positive correlation (r = 0. 644, r = 0. 645). Conclusions: There are both p16 ^InK4a and Ki67 expressions in CIN in young women , and expressions of p16 ^InK4a and ki67 were both posi- tively correlated with the grade of CIN lesion. The results demonstrate their role as markers in supporting the diagnosis of grade of CIN lesion.
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