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作 者:廖书杰[1] 袁兵[2] 胡晓继[1] 周蓉 卢运萍[1] 王世宣[1] 马丁[1]
机构地区:[1]华中科技大学同济医学院附属同济医院妇产科,武汉430032 [2]云南省第一人民医院呼吸内科,昆明650000 [3]华中科技大学同济医学院附属同济医院肾内科,武汉430030
出 处:《肿瘤》2008年第4期317-321,共5页Tumor
基 金:国家重点基础研究发展计划项目(九七三计划)(编号:2002CB513100)
摘 要:目的:通过检测PI3K、AKT、P-AKT和Ki67在宫颈癌中的表达,探讨其与宫颈病变发生发展的关系及相关的临床意义。方法:应用免疫组织化学SP法检测宫颈癌组织及其正常组织中PI3K、AKT、p-AKT和Ki67的表达。结果:(1)宫颈癌中PI3K、AKT、p-AKT和Ki67蛋白的阳性表达率较宫颈上皮内瘤样病变(cervical intraepithelial neoplasia,CIN)各级的高,差异有统计学意义(P<0.05),鳞癌与腺癌无差别;CIN各级中PI3K、AKT和p-AKT的阳性表达率较正常宫颈组织高,差异有统计学意义(P<0.05),且这种差异随着CIN级别的递增而增大。(2)CIN各级宫颈组织中PI3K、AKT、p-AKT表达与Ki67表达有关。(3)PI3K和p-AKT表达与宫颈癌分化程度及临床分期明显相关,但与年龄、组织学类型和淋巴结转移无关。Ki67表达与各临床病理指标无明显相关性。结论:PI3K、AKT、P-AKT和Ki67的异常表达参与了宫颈癌的发生发展,与细胞增殖能力加强有关。Objective:To detect the expressions of PI3K, AKT, p-AKT, and Ki67 in cervical intraepithelial neoplasia (CIN) and cervical carcinoma and explore their relation with the occurrence and development of cervical diseases and the clinical significance. Methods:The expression of PI3K, AKT, p-AKT, and Ki67 in cervical intraepithelial neoplasia (CIN) and cervical carcinoma were detected by immunohistochemical SP methods. Results: ( 1 ) The expressions of PI3 K, AKT, p-AKT, and Ki67 protein were significantly higher in cervical carcinoma than CIN and normal cervical tissues. The difference was significant ( P 〈 0.05 ). There was no significant difference between adenocarcima and squamous adenocarcinoma. CIN tissues had higher expressions of PI3K, AKT, p-AKT, and Ki67 proteins than normal control ( P 〈0.05 ) and the difference was increased with the elevated grade of CIN. (2) The expressions of PI3K, AKT, and p-AKT correlated with Ki67 in CIN tissues at various grades. (3) The expressions of PI3K and p-AKT had correlation with histological differentiation and clinical stage, but not with age, histological subtype, lymph node metastases. Expression of Ki67 was not associated with clinicopathological parameters. Conclusion:The aberrant expressions of PI3K, AKT, p-AKT, and Ki67 were involved in the occurrence and development of cervical cancer and related with the enhanced proliferation of tumor cells.
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