期刊文献+
共找到3篇文章
< 1 >
每页显示 20 50 100
SIRT-1 SRGAP1 NCAPH在宫颈癌中的表达及对患者预后的预测价值
1
作者 张剑 《中国妇幼保健》 CAS 2024年第24期4950-4954,共5页
目的分析沉默信息调节因子家族-1(SIRT-1)、Slit-Robo GTP酶激活蛋白质1(SRGAP1)、NCAPH在宫颈癌中的表达及对患者预后的预测价值。方法选择2020年10月—2021年10月天津医科大学第二医院收治的宫颈癌患者60例为研究组,同期收治的良性宫... 目的分析沉默信息调节因子家族-1(SIRT-1)、Slit-Robo GTP酶激活蛋白质1(SRGAP1)、NCAPH在宫颈癌中的表达及对患者预后的预测价值。方法选择2020年10月—2021年10月天津医科大学第二医院收治的宫颈癌患者60例为研究组,同期收治的良性宫颈病变患者60例为对照组,所有患者均在本院进行手术切除病理组织。通过免疫组化法检测病理组织标本SIRT-1、SRGAP1、NCAPH阳性表达率,分析SIRT-1、SRGAP1、NCAPH与临床特征的关系,采用logistic回归分析并绘制生存曲线,分析SIRT-1、SRGAP1、NCAPH不同表达患者预后情况。结果与对照组相比,研究组SIRT-1(预后良好vs预后不良)(21.67 vs.71.43 vs.87.50)、SRGAP1(23.33 vs.71.43 vs.93.75)、NCAPH(26.67 vs.57.14 vs.90.63)阳性率较高,且研究组中预后不良宫颈癌患者SIRT-1(87.50 vs.71.43)、SRGAP1(93.75 vs.71.43)、NCAPH(90.63 vs.57.14)阳性率高于预后良好患者(P<0.05)。SIRT-1、SRGAP1、NCAPH阳性表达率与临床分期、浸润深度、组织分化程度、淋巴结转移、肿瘤直径有关,且呈正相关(P<0.05)。临床分期、浸润深度、组织分化程度、淋巴结转移、肿瘤直径、SIRT-1、SRGAP1、NCAPH为宫颈癌预后的危险因素。随访1年,失访2例,58宫颈癌患者1年生存率为63.79%,SIRT-1、SRGAP1、NCAPH阳性表达患者生存率低于SIRT-1、SRGAP1、NCAPH阴性表达患者(P<0.05)。ROC曲线显示,三项联合对宫颈癌预后不良和预测价值高于SIRT-1、SRGAP1、NCAPH单项诊断(P<0.05)。结论宫颈癌组织中SIRT-1、SRGAP1、NCAPH阳性率较高,且与临床分期、浸润深度、组织分化程度、淋巴结转移、肿瘤直径及预后相关,联合检测对宫颈癌患者预后的预测价值较高。 展开更多
关键词 沉默信息调节因子家族-1、Slit-Robo GTP酶激活蛋白质1 NCAPH 宫颈癌 预后
原文传递
茶多酚抑制肿瘤细胞增殖的分子机制研究新进展 被引量:16
2
作者 罗非君 《国外医学(生理病理科学与临床分册)》 2001年第4期251-253,共3页
茶多酚具有抗癌作用 ,但其分子机制尚未明了。近年来 ,茶多酚抑制肿瘤细胞增殖的研究取得了许多突破性进展。茶多酚能下调肿瘤细胞DNA拓扑异构酶与DNA引物酶的活性 ,抑制DNA的复制 ;茶多酚可明显促进WAF1/p2 1,KIP1/p2 7,p16,p18和p5 3... 茶多酚具有抗癌作用 ,但其分子机制尚未明了。近年来 ,茶多酚抑制肿瘤细胞增殖的研究取得了许多突破性进展。茶多酚能下调肿瘤细胞DNA拓扑异构酶与DNA引物酶的活性 ,抑制DNA的复制 ;茶多酚可明显促进WAF1/p2 1,KIP1/p2 7,p16,p18和p5 3蛋白表达 ,抑制cyclinD1,CDK4和CDK6表达 ,使细胞周期发生G1/S与G2 /M阻滞 ;茶多酚也能通过干预AP 1与NF κB信号转导通路、调控细胞内氧化还原状态、抑制端粒酶活性等多种机制导致肿瘤细胞增殖抑制。 展开更多
关键词 茶多酚 激活蛋白质1 信号转导 细胞周期 肿瘤 预防 治疗 肿瘤细胞增殖
下载PDF
Imbalanced expression of mitogen-activated protein kinase phosphatase-1 and phosphorylated extracellular signal-regulated kinases in lung squamous cell carcinoma 被引量:2
3
作者 Kai WANG Min ZHANG +3 位作者 Ying-ying QIAN Zhe-vuan DING Jun-hui LV Hua-hao SHEN 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2011年第10期828-834,共7页
Objective: Mitogen-activated protein kinases (MAPKs) are correlated with a more malignant phenotype in many cancers. This study was designed to evaluate the predictive value of the expression of MAPK phosphatase-1 ... Objective: Mitogen-activated protein kinases (MAPKs) are correlated with a more malignant phenotype in many cancers. This study was designed to evaluate the predictive value of the expression of MAPK phosphatase-1 (MKP-1) and phosphorylated extracellular signal-regulated kinase 1/2 (p-ERKl/2), as the key regulatory mechanism of the MAPKs, in lung squamous cell carcinoma (SCC). Methods: We assessed the expressions of MKP-1 and p-ERK1/2 in twenty subjects at different differentiation degree of SCC and five normal lungs by immunohistochemistry and real-time reverse transcriptase polymerase chain reaction (RT-PCR) analysis. Results: Immunohistochemistry and real-time RT-PCR assay showed that the expression of MKP-1 was gradually decreased as tissue type went from normal lung tissues to increasingly undifferentiated carcinoma, and it was negatively correlated with tumor differentiation (P〈0.01). However, the expression of p-ERK1/2 or ERKl/2 was gradually increased as tissue type went from normal lung tissues to increasingly undifferentiated carcinoma, and it was positively correlated with tumor differentiation (P〈0.01). Conclusions: Our data indicates the relevance of MKP-1 and p-ERK1/2 in SCC as a potential positive and negative prognostic factor. The imbalanced expression of MKP-1 and p-ERKl/2 may play a role in the development of SCC and these two molecules may be new targets for the therapy and prognosis of SCC. 展开更多
关键词 Mitogen-activated protein kinase phosphatase-1 (MKP-1 Extracellular signal-regulated kinase (ERK) Lung squamous cell carcinoma (SCC) Prognostic factor
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部