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细胞周期蛋白E

细胞周期蛋白E的相关文献在1999年到2022年内共计344篇,主要集中在肿瘤学、基础医学、中国医学 等领域,其中期刊论文162篇、专利文献228057篇;相关期刊114种,包括医学分子生物学杂志、中国病理生理杂志、中华临床医师杂志(电子版)等; 细胞周期蛋白E的相关文献由962位作者贡献,包括T·J·古兹、M·P·德怀尔、K·帕鲁奇等。

细胞周期蛋白E—发文量

期刊论文>

论文:162 占比:0.07%

专利文献>

论文:228057 占比:99.93%

总计:228219篇

细胞周期蛋白E—发文趋势图

细胞周期蛋白E

-研究学者

  • T·J·古兹
  • M·P·德怀尔
  • K·帕鲁奇
  • R·J·多尔
  • V·M·吉里亚瓦拉布汉
  • 周发林
  • 江世贵
  • 邱丽华
  • V·D·特兰
  • Z·M·何
  • 期刊论文
  • 专利文献

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    • 刘艳; 卞伟; 肖虹(审校)
    • 摘要: 细胞周期蛋白E1(Cyclin E1,CCNE1)基因扩增是卵巢高级别浆液性癌(high-grade serous ovarian carcinoma,HGSOC)最常见的拷贝数变异之一,扩增率为20%左右。CCNE1基因扩增不仅参与HGSOC的早期癌前病变,促进恶性肿瘤的发生、发展,还可引起细胞周期紊乱和染色体不稳定,从而增加HGSOC的铂类耐药性和复发率,最终导致患者的化疗效果不佳和预后较差。为改善CCNE1扩增的HGSOC患者的预后和生活质量,在暂时没有CCNE1扩增的HGSOC的靶向治疗药物的情况下,使用细胞周期蛋白依赖性激酶2(cyclin-dependent kinases 2,CDK2)小分子抑制剂或者多腺苷二磷酸核糖聚合酶[poly(ADP-ribose)polymerase,PARP]抑制剂与其他药物联合治疗,一定程度上能有效地抑制肿瘤细胞的增殖活性,促进肿瘤细胞死亡。因此,从CCNE1扩增对HGSOC的早期发病机制的影响和产生铂类耐药的角度上来说,CCNE1基因有望成为HGSOC的潜在治疗靶标和预后评价生物学指标,在改善患者的治疗和预后方面具有重要意义。
    • 罗振强; 张军艳; 李军义
    • 摘要: 胃癌前病变被认为是慢性萎缩性胃炎伴发肠上皮化生或者异常增生引起的病理学症状,其发展恶化到一定程度会演变成胃癌,因此及早发现并治疗胃癌前病变对于预防胃癌发生、减少其发病率具有重要的意义。西医学对于胃癌前病变的机制尚不清楚,研究表明[1]生长激素(GH)对胃肠道黏膜上皮细胞的代谢、生长和分化有调节作用,表皮生长因子(EGF)对消化道的生长、分化及成熟具有重要的调节作用,细胞周期蛋白E(cyclin E)、B细胞淋巴瘤/白血病?鄄XL(Bcl?鄄XL)、肿瘤坏死因子受体相关因子1(TRAF1)与胃癌的发生、发展有着密切的关系。中医学[2]认为胃癌前病变归属“胃脘痛”“痞满”等范畴,病因诸多,多由外感六淫、饮食不节、情志不畅、劳逸不调,内因脾虚等引起。本研究采用丹芪祛瘀止痛颗粒对胃癌前病变患者进行治疗,探讨其临床治疗疗效及对GH、EGF、TRAF1、cyclin E、Bcl?鄄XL等因子表达水平的影响,现报告如下。
    • 胡倩; 郭华荣
    • 摘要: 细胞周期蛋白E (Cyclin E)是细胞周期蛋白家族成员之一,其在细胞周期活动中发挥重要作用,本文对Cyclin E的结构、生物学功能与作用机制及其在海洋无脊椎动物中的研究进展进行了综述和展望。
    • WANG Li-Ying; BIAN Liang-Qi; SU Xiao-Wei; SU Hai-Yan; LIU Xu; LIU Nan-Nan
    • 摘要: 研究了牛磺酸(Taurine,Tau)对新生大乳鼠心肌成纤维细胞(Myofibroblasts,myoFbs)增殖的抑制作用,并探讨其作用机制.应用血管紧张素Ⅱ(AngiotensinⅡ,AngⅡ)诱导体外培养新生大乳鼠的myoFbs增殖,建立了心肌纤维化(Myofibrosis,MF)模型,基于甲基偶氮唑盐法检测myoFbs增殖.结果表明,不同浓度(0.03、0.06和0.12 mol/L)Tau均可显著抑制myoFbs增殖,且呈现出剂量依赖性.进一步应用免疫细胞化学、激光共聚焦显微镜及ELISA方法检测了活性氧(Reactive oxygen species,ROS)、细胞周期蛋白E(Cell cycle protein E,CyclinE)、核转录因子 κBp65(Nuclear factor-kappa Bp65,NF-κBp65)及转化生长因子 β1(Transforming growth factor-β1,TGF-β1)在myoFbs中的的表达及含量.研究结果表明,Tau是通过减少ROS的产生及TGF-β1的表达、抑制NF-κBp65的核转位及CyclinE的表达,抑制myoFbs增殖,起到抗MF的作用.
    • 程伟; 马丁; 杨彬; 尚吉文; 米振国; 张雁钢
    • 摘要: Objective To investigate the expressions of metallothionein-2A (MT-2A), E-cadherin, interleukin-6 (IL-6), cyclin E, proliferating cell nuclear antigen (PCNA) and bcl-2 in prostate cancer tissues and their correlation with biochemical recurrence of prostate cancer. Methods Tissue specimens from 128 cases of prostate cancer who underwent radical prostatectomy in Shanxi Dayi Hospital from October 2012 to October 2017 were processed and transferred into tissue microarrays, the clinicopathological parameters of patients were also recorded. The expression levels of MT-2A, E-cadherin, IL-6, cyclin E, PCNA and bcl-2 were detected by immunohistochemical avidin-biotin complex (ABC) staining. The correlation between different molecular markers and biochemical recurrence of prostate cancer was analyzed. Results The biochemical recurrence rate of 128 patients with prostate cancer was 30.5% (39/128). The biochemical recurrence rates of low-risk, intermediate-risk and high-risk prostate cancer patients were 14.8%(8/54), 38.7%(24/62) and 58.3% (7/12), respectively. The risk classification and pathological T stage of patients with prostate cancer were associated with the expressions of MT-2A, cyclin E, IL-6 and E-cadherin (all P< 0.05). Multivariate Cox risk model showed that the high risk classification (HR= 1.81, 95%CI 1.56-2.19, P=0.042), MT-2A positive expression (HR= 2.01, 95%CI 1.08-3.15, P= 0.005), cyclin E positive expression (HR= 1.79, 95%CI 1.08-2.21, P= 0.042) and E-cadherin negative expression (HR= 1.92, 95% CI 1.22-2.45, P= 0.020) were the independent risk factors for biochemical recurrence of prostate cancer. Conclusion The expression of MT-2A, cyclin E and E-cadherin may serve as independent predictors for biochemical recurrence of prostate cancer.%目的 探讨金属硫蛋白2A(MT-2A)、E钙黏蛋白(E-cadherin)、白细胞介素6(IL-6)、细胞周期蛋白E(cyclin E)、增殖细胞核抗原(PCNA)和抗凋亡蛋白bcl-2在前列腺癌组织中的表达及其与前列腺癌生化复发之间的相关性.方法 收集2012年10月至2017年10月于山西大医院接受前列腺癌根治性手术的128例患者的前列腺癌组织标本,记录患者的临床数据.制作组织芯片,采用免疫组织化学生物素-亲和素复合物(ABC)染色法检测芯片组织MT-2A、E-cadherin、IL-6、cyclin E、PCNA和bcl-2的表达水平,并分析不同分子标志物与前列腺癌生化复发之间的相关性.结果 128例前列腺癌患者生化复发率为30.5%(39/128),低危、中危和高危前列腺癌患者生化复发率分别是14.8%(8/54)、38.7%(24/62)和58.3%(7/12).前列腺癌患者危险分级和病理学T分期与MT-2A、cyclin E、IL-6、E-cadherin表达均有关(均P<0.05).多因素Cox风险模型结果显示,高危险分级(HR=1.81,95%CI 1.56~2.19,P=0.042)、MT-2A阳性表达(HR=2.01,95%CI 1.08~3.15,P=0.005)、cyclin E阳性表达(HR=1.79,95%CI1.08~2.21,P=0.042)和E-cadherin阴性表达(HR=1.92,95%CI 1.22~2.45,P=0.020)是前列腺癌生化复发的独立危险因素.结论 前列腺癌组织中MT-2A、cyclin E和E-cadherin是预测前列腺癌生化复发的重要分子标志物.
    • 廖铭心; 刘瑶; 蔡僮; 方文
    • 摘要: 目的 探讨沉默核内不均一核糖核蛋白A2/B1(hnRNP A2/B1)基因后对人宫颈癌Hela细胞中细胞周期蛋白(cyclin) D1及cyclin E的表达及裸鼠移植瘤生长的影响.方法 运用慢病毒转染沉默Hela细胞中的hnRNP A2/B1基因并用成功沉默后的细胞建立体外细胞及体内移植瘤模型.用Western blot检测细胞及移植瘤中的cyclin D1/E的表达情况,四甲基偶氮唑蓝(MTT)检测细胞的增殖能力,免疫组织化学分析各组移植瘤组织中增殖相关蛋白增殖细胞抗原(PCNA)及Ki-67的表达水平并用HE染色分析组织的病理形态.结果 沉默hnRNP A2/B1基因后Hela细胞中cyclin D1/E表达降低,裸鼠移植瘤PCNA及Ki-67相较未沉默组表达降低,裸鼠移植瘤的生长明显受到抑制,差异均有统计学意义(P<0.05).结论 沉默hnRNP A2/B1基因后能降低宫颈癌Hela细胞中cyclin D1及cyclin E的表达,抑制肿瘤细胞增殖及生长.
    • 韦; 张建; 林才志; 张文富
    • 摘要: [目的]探讨中西医结合治疗慢性萎缩性胃炎伴癌前病变的疗效及对患者外周血T淋巴细胞亚群、细胞周期蛋白E(Cyclin E)、E-钙粘蛋白(E-cadherin)和基质金属蛋白酶-9(MMP-9)表达的影响.[方法]将84例确诊为萎缩性胃炎伴癌前病变患者按照随机数字表法分为2组各42例,对照组予常规西药治疗,观察组在对照组基础上予口服养胃祛浊汤,两组均治疗观察24周.[结果]观察组总有效率为59.52%,高于对照组的30.95%,两组比较有显著性差异(P<0.05);观察组胃镜表现及病理组织学检测相关指标均优于对照组(P<0.05);观察组外周血中CD3+、CD4+、CD8+细胞优于对照组,观察组治疗后Cyclin E和MMP-9蛋白表达明显低于对照组,而E-cadherin蛋白表达高于对照组(P<0.05).[结论]中西医结合对慢性萎缩性胃炎伴癌前病变具有较好疗效,可调整外周血T淋巴细胞亚群的表达,改善细胞周期蛋白E、E-cadherin及MMP-9表达,改善患者的炎症反应和癌前病变状态.
    • 韦; 张建; 林才志; 张文富
    • 摘要: [目的]探讨中西医结合治疗慢性萎缩性胃炎伴癌前病变的疗效及对患者外周血T淋巴细胞亚群、细胞周期蛋白E(Cyclin E)、E-钙粘蛋白(E-cadherin)和基质金属蛋白酶-9(MMP-9)表达的影响。[方法]将84例确诊为萎缩性胃炎伴癌前病变患者按照随机数字表法分为2组各42例,对照组予常规西药治疗,观察组在对照组基础上予口服养胃祛浊汤,两组均治疗观察24周。[结果]观察组总有效率为59.52%,高于对照组的30.95%,两组比较有显著性差异(P〈0.05);观察组胃镜表现及病理组织学检测相关指标均优于对照组(P〈0.05);观察组外周血中CD3^+、CD4^+、CD8^+细胞优于对照组,观察组治疗后Cyclin E和MMP-9蛋白表达明显低于对照组,而E-cadherin蛋白表达高于对照组(P〈0.05)。[结论]中西医结合对慢性萎缩性胃炎伴癌前病变具有较好疗效,可调整外周血T淋巴细胞亚群的表达,改善细胞周期蛋白E、E-cadherin及MMP-9表达,改善患者的炎症反应和癌前病变状态。
    • 周娜; 赵雅宁; 李佳宁; 王静; 李建民; 刁莉君; 陈长香
    • 摘要: Objective:To investigate the effect of different intensity of treadmill running precondition on learning and memory ability and the expression of cell cycle protein in rats after global cerebral ischemia reperfusion.Method:Eighty healthy male SD rats were randomly divided into:normal group (n=20),model group (n=20),intensity Ⅰ group (n=20) and intensity Ⅱ group (n=20).Two weeks before surgery,the rats of the intensity Ⅰ group and intensity Ⅱ group were trained on treadmill.The speed of intensity Ⅰ group was 20m/min*30 (30%VO2max).The speed of intensity Ⅱ group was 10m/min at first,then accelerated to 19.3m/min in 3minutes (70%VO2max) and hold the speed until the rats get exhausted.Global cerebral ischemia model was formed by improved four-vessel occlusion according to Pulsinelli's method.The morphological changes of neural cells in hippocampus at each time point were observed with HE staining;The expressions of CyclinA and CyclinE at each time point were detected with immunohistochemical staining;Visual-spatial memory of rats was measured with Morris water-maze test at 48h after modeling.Result:Comparing with normal group,the rates of survival neurons and,the times of crossing the area where the platform had been located on previous trials decreased,the escape latency of rats and,the expression of CyclinE and CyclinA significantly increased in all other groups (P < 0.05).Furthermore,the rates of survival neurons,the times of crossing the area where the platform had been located on previous trials were less in model group than in intensity Ⅰ group (P< 0.05),and more than in intensity Ⅱ group (P < 0.05).In model group,the escape latency of rats and the expression of CyclinE and CyclinA were more than in intensity Ⅰ group (P < 0.05),and less than in intensity Ⅱ group (P< 0.05).Conclusion:The moderate intensity exercise precondition could protect nerve tissue and improve the function of learning and memory after global cerebral ischemia.,while the High intensity exercise may be negative,which may be relate to the regulation of cell cycle protein.%目的:探讨不同强度跑台运动预处理对脑缺血大鼠学习记忆及细胞周期蛋白表达的影响.方法:将80只健康雄性SD大鼠随机分为正常组(n=20)、模型组(n=20)、强度Ⅰ组(n=20)和强度Ⅱ组(n=20).造模前2周开始对强度Ⅰ和强度Ⅱ组大鼠进行跑台运动训练,其中强度Ⅰ组设置为20m/min*30min,强度Ⅱ组使大鼠运动强度递增,在3min内南10m/min的速度提高到预定的19.3m/min的速度,保持速度直到力竭.用四血管阻断法(Pulsinelli 4VO法)制备全脑缺血模型,分别在建模后3h、6h、24h、48h进行HE染色法观察各组大鼠脑组织神经元细胞形态的变化情况,免疫组织化学染色法检测各组大鼠脑组织海马区细胞周期蛋白A(CyclinA)和细胞周期蛋白E(CyclinE)的表达情况.建模后48h大鼠在处死前采用水迷宫检测各组大鼠学习记忆功能.结果:与正常组比较,其他三组神经元存活数日显著减少,逃避潜伏期明显延长,穿台次数明显减少,差异均有显著性意义(P<0.05).其中,模型组神经元存活数目、穿台次数明显少于强度Ⅰ组(P<0.05),显著高于强度Ⅱ组(P<0.05),逃避潜伏期明显长于强度Ⅰ组(P<0.05),显著短于强度Ⅱ组(P<0.05).与正常组比较,模型组各时间点CyclinA、CyclinE的表达水平明显增加(P<0.05).这两个因子的表达在模型组中多于强度Ⅰ组(P<0.05),但明显少于强度Ⅱ组(P< 0.05).结论:中强度的跑台运动可保护脑组织,改善全脑缺血大鼠学习记忆功能,但高强度的运动会产生不良反应,可能与调控全脑缺血再灌注大鼠细胞周期蛋白的表达有关.
    • 李伟; 张庚; 王海伦; 王亮
    • 摘要: Objective To explore the effect of the expression of cell cycle regulators on the development and prognosis of colorectal carcinoma.Methods The surgicall resected tissues from 128 cases of colorectal cancer were collected in our hospital from June 2012-December 2015 December.The expression levels of Cyclin E,proliferation cell nuclear antigen (Ki-67) and matrix metalloproteinase (MMP)-9 were detected by immunohistochemieal staining in the large intestine mucosa from 128 cases of carcinoma and 24 samples of normal mucosa.x2 test,single factor analysis of variance,Kaplan-Meier survival rate curve analysis and Log-rank test were applied.P < 0.05 was considered to be statistically significant difference.Results The positive rate of Cyclin E,Ki-67 and MMP-9 was significalntly higher in colorectal carcinoma than in normal mucosa (x2 =5.203,P =0.013).The expression of Cyclin E in Duke's stage A was markedly higher than in Duke's stages B,C and D (x2 =10.331,P =0.001),and it was higher in cases with negative lymph node metastasis than in those with positive lymph node metastasis (x2 =6.732,P =0.005).The expression of Cyclin E was not correlated with the prognosis of the cases with lymph node metastasis.The down-regulated expression or deficiency of MMP-9 was related to advanced Duke's stages (x2 =7.201,P =0.003) and lymph node metastasis (x2 =12.072,P =0.000).The Ki-67 expression was not associated with the carcinoma localization,advanced Duke's stages and prognosis.There were 44 deaths from 128 patients,accounting for 39.29%,with 24,14 and 36 cases positive for,and 20,30 and 8 cases negative for Cyclin E,Ki-67 and MMP-9 expression,respectively.The 5-year survival rate in Cyclin E positive and negative expression groups was 63.64% and 56.52% respectively,with no significant difference (x2 =0.958,P =0.273).The 5-year survival rate in MMP-9 positive expression group was 73.33%,significantly higher than that in MMP-9 negative group (46.15%,x2 =3.143,P =0.035).The 5-year surfival rate in Ki-67 positive group (61.70%) and negative group (55.56%) showed no significant difference (x2 =0.827,P=0.419).The expression of Cyclin E was positively correlated with Ki-67 (r =0.391,P =0.019),MMP-9 and Ki-67 showed nosignificant correlation (r =-0.109,P =0.387),and MMP-9 and Cyclin E expression had no significant correlation (r =-0.168,P =0.183).Conclusion The overexpression of Cyclin E and decline or deficiency of MMP-9 expression might accelerate the progression of the cell cycle and promote the carcinogenesis of colorectal carcinoma.The overexpression of Cyclin E might be a relatively early event in initiation of colorectal carcinoma.The decline or deficiency of MMP-9 expression might promote the development and metastasis of colorectal carcinoma,and it could be an indicator for unfavorable prognosis.%目的 观察细胞周期调控因子蛋白表达在大肠癌发生、发展中的作用及对预后的影响.方法 收集手术切除的大肠癌128例,采用免疫组织化学染色,对128例大肠癌和24例正常大肠黏膜细胞周期蛋白E(Cyclin E)、细胞核增殖抗原(Ki-67)、基质金属蛋白酶(MMP)-9进行检测.采用x2检验、单因素方差分析和Kaplan-Meier生存率曲线分析及Log-rank检验.结果 大肠癌与正常大肠黏膜比较Cyclin E、Ki-67阳性表达率明显增高,MMP-9阳性表达率明显降低(x2=5.203,P=0.013).Duke's A期Cyclin E阳性表达率明显高于Duke's B、C、D期(x2=10.331,P=0.001),无淋巴结转移明显高于有淋巴结转移者(x2 =6.732,P=0.005);Cyclin E的表达与大肠癌患者的预后无明显相关.MMP-9表达下降或缺乏.与大肠癌的Duke's分期、淋巴结转移有关(x2=7.201,P=0.003),且其5年生存率显著降低(x2=12.072,P=0.000).Ki-67表达与大肠癌部位、Duke's分期及患者预后无明显相关.128例患者中因本病死亡者44例,占39.29%,包括Cyclin E、Ki-67、MMP-9阳性表达各24、14、36例,阴性表达各20、30、8例.Cyclin E阳性、阴性表达组5年生存率较接近,分别为63.64%、56.52%,差异无统计学意义(x2=0.958,P=0.273).MMP-9阳性表达组5年生存率为73.33%,明显高于MMP-9阴性组的46.15%(x2=3.143,P=0.035).Ki-67阳性表达组5年生存率(61.70%)与阴性表达组(55.56%)较接近,两组间差异无统计学意义(x2=0.827,P=0.419),128例患者中,Cyclin E与Ki-67的表达呈正相关(r=0.391,P=0.019),MMP-9与Ki-67表达无相关(r=-0.109,P=0.387),MMP-9与Cyclin E表达无明显相关(r=-0.168,P=0.183).结论 Cyclin E过表达及MMP-9蛋白表达下降或缺失可能会加速细胞周期的转化,并参与大肠癌的发生;Cyclin E过表达可能是大肠癌形成过程中较早的分子事件.MMP-9蛋白表达下降或缺失可能促进了大肠癌的发展及转移,且提示为患者预后不良的危险因素.
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