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端粒,末端转移酶

端粒,末端转移酶的相关文献在1994年到2021年内共计363篇,主要集中在肿瘤学、基础医学、内科学 等领域,其中期刊论文363篇、专利文献113399篇;相关期刊105种,包括中国病理生理杂志、中华病理学杂志、中华实验外科杂志等; 端粒,末端转移酶的相关文献由1361位作者贡献,包括张波、侯琳、张洹等。

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论文:363 占比:0.32%

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论文:113399 占比:99.68%

总计:113762篇

端粒,末端转移酶—发文趋势图

端粒,末端转移酶

-研究学者

  • 张波
  • 侯琳
  • 张洹
  • 崔京远
  • 王洁
  • 高晓东
  • 何冬梅
  • 孙建方
  • 徐秀莲
  • 房殿春
  • 期刊论文
  • 专利文献

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    • 徐保华; 崔世超; 崔京远; 袁志丽; 司君圣; 刘杰
    • 摘要: 目的:探讨人端粒酶逆转录酶(hTERT)基因rs2736098、rs2075786和rs2736100位点单核苷酸多态性(SNP)与结肠癌遗传易感性的关系.方法:采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法对186例结肠癌患者和194例结肠腺瘤患者(病例组)以及随机匹配的406例健康体检行结肠镜检查未见明显异常者(对照组)进行基因多态性分析.结果:rs2736098、rs2075786位点各基因型在病例组和对照组中的频率分布差异无统计学意义(P>0.05),结肠癌组rs2736100位点GG基因型频率显著高于健康对照组及结肠腺瘤组(29.03%vs 16.50%、18.04%,P<0.05),携带GG基因型者罹患结肠癌风险增加2.216倍(95%CI:1.393-3.527).结论:hTERT基因rs2736100位点基因多态性与结肠癌遗传易感性相关.
    • 刘千琪; 周桥; 陈铌; 尹晓雪; 邹艳; 余天平; 龚静; 陈雪芹; 聂玲; 徐苗; 张孟尼
    • 摘要: 目的 探讨弥漫浸润性胶质肿瘤中端粒酶逆转录酶(TERT)及异柠檬酸脱氢酶(IDH)基因热点突变情况及二者结合的预后价值.方法 采用Sanger测序法检测四川大学华西医院2012至2014年手术的236例胶质瘤标本(WHOⅠ~Ⅳ级肿瘤分别为16、89、72和59例)中TERT基因启动子区(228位点和250位点)、IDH1(132密码子)和IDH2(172密码子)突变情况,分析这些突变与患者预后的关系.结果 WHOⅠ级16例毛细胞型星形细胞瘤中均未检出IDH和TERT基因突变.WHOⅡ~Ⅳ级的220例弥漫浸润性胶质肿瘤中,年龄≥40岁患者TERT突变比例(60.8%,93/153)明显高于<40岁患者(32.8%,22/67;P<0.01),少突胶质瘤中TERT突变率(87.5%,56/64)明显高于星形细胞瘤(37.8%,59/156;P<0.01).年龄<40岁、IDH1突变和少突胶质瘤为弥漫浸润性胶质肿瘤预后好的因素.TERT突变不能单独提示胶质瘤预后.TERT和IDH1突变联合检测可将弥漫浸润性胶质瘤分为4个分子亚组:IDH(+)/TERT(+)组、IDH(+)/TERT(-)组、IDH(-)/TERT(-)组和IDH(-)/TERT(+)组,4组间具有明显预后差异,IDH(+)/TERT(+)组患者预后最好,IDH(-)/TERT(+)组患者预后最差.结论 IDH和TERT基因突变状态可细化胶质瘤患者预后分组,特别是可将IDH1野生型的病例进一步进行预后亚组划分,具有较好的临床应用价值.%Objective To investigate the status and prognostic significance of TERT and IDH1/2 genes mutations in diffusely infiltrating gliomas. Methods Hot spot mutations of TERT and IDH1/2 genes were detected by DNA sequencing in 236 cases of gliomas at West China Hospital from 2012 to 2016, including pilocytic astrocytoma ( WHO grade Ⅰ, 16 cases ) , diffuse astrocytoma and oligodendroglioma ( WHO grade Ⅱ,89 cases) , anaplastic astrocytoma and oligodendroglioma ( WHO grade Ⅲ,72 cases) and glioblastoma ( WHO grade Ⅳ, 59 cases ) . The prognostic significance of TERT and IDH1/2 hot spot mutations was evaluated. Results No IDH or TERT mutations were detected in pilocytic gliomas. TERT promoter mutation frequency was higher in patients aged ≥40 years( 60. 8%,93/153) than in patients aged<40 years ( 32. 8%, 22/67;P<0. 01 ) . TERT promoter mutation rate was also significantly higher in oligodendroglioma ( 87. 5% , 56/64 ) than that in astrocytoma ( 37. 8%, 59/156;P<0. 01 ) . Young age (<40 years) , oligodendroglioma and IDH1 mutation were favorable prognostic factors for diffusely infiltrating astrocytic and oligodendroglial tumors. TERT mutation alone was not of prognostic significance. Diffusely infiltrating astrocytic and oligodendroglial tumors were divided into four molecular subtypes according to TERT and IDH1 mutation status:IDH(+)/TERT(+) , IDH(+)/TERT(-) , IDH(-)/TERT(-) and IDH (-)/TERT(+) . There was significant prognostic difference among the 4 subtypes. Conclusions Combined IDH and TERT gene mutation analysis may be useful for prognostic subgrouping. Notably, IDH1 wild-type cases can be further subdivided into TERT(+) or (-) subgroups with significant prognostic difference.
    • 崔伟丽; 褚志予; 马红; 崔京远; 亓玉琴
    • 摘要: 目的:探讨人类端粒酶逆转录酶(hTERT)基因位点(rs2736100、rs2853676)单核苷酸多态性(SNP)与青岛地区人群乙肝肝癌的易感性.方法:采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)检测来自青岛地区的肝癌患者1 65例、非肝癌乙肝病毒感染者195例、健康对照者402例hTERT基因型分布.结果:(1)肝癌组患者rs2736100位点GG基因型频率显著高于对照组、非肝癌HBV感染者及所有非HCC者(均P<0.05),携带GG基因型者罹患肝癌的风险分别增加至2.13倍、2.17倍和2.14倍.(2)肝癌组患者rs2853676位AA基因型频率显著高于对照组、非肝癌HBV感染者及所有非HCC者(均P<0.05),携带AA基因型者罹患肝癌的风险分别增加至3.42倍、2.39倍和3.02倍.结论:hTERT rs2736100和rs2853676位点基因多态性与肝癌易感性相关.%Objective:To explore the correlation between several single-nucleotide polymorphisms (SNPs) loci on the gene of human telomerase reverse transcriptase (hTERT)(including rs2736100、rs2853676) and the susceptibility to Hepatocellular carcinoma in Qingdao area.Methods:This case-control study included 165 diagnosed Hepatocellular carcinoma,195 with chronic hepatitis B and 402 Healthy people.Polymerase chain restriction fragment length polymorphism were performed to analyze the genotype of the loci on the gene of hTERT.Results:The frequency of TT genotype on rs2736100 were higher in the Hepatocellular carcinoma group compared to the control group、chronic hepatitis B and no HCC people(P<0.05).The additive odds ratio of TT genotype for the risk of Hepatocellular carcinoma was 2.13、2.17 and 2.14.The frequency of AA genotype on rs2853676 were higher in the Hepatocellular carcinoma group compared to the control group、chronic hepatitis B and no HCC people (P<0.05).The additive odds ratio ofTT genotype for the risk of Hepatocellular carcinoma was 3.42、2.39 and 3.02.Conclusion:There was a relationship between hTERT rs2736100 and rs2853676 polymorphism and susceptibility to Hepatocellular carcinoma.
    • 冯玉环; 易建平; 陈莹; 郑寰宇; 靖丽华
    • 摘要: 目的 探讨磷酸化蛋白激酶B1(pAkt1)和人端粒酶反转录酶(hTERT)在卵巢上皮性癌(EOC)中的表达及其与患者预后的关系,分析pAkt1和hTERT表达的相关性.方法 选取2012年1月至2016年12月在河北省唐山工人医院治疗的92例EOC患者.采用免疫组织化学法检测患者肿瘤组织中hTERT和pAkt1蛋白的表达,分析pAkt1、hTERT蛋白表达的相关性及与预后的关系.结果 92例EOC患者中,pAkt1阳性表达68例(73.9%),hTERT阳性表达52例(56.5%).pAkt1、hTERT蛋白在EOC中的表达无相关性(r=0.284,P=0.633).pAkt1、hTERT蛋白表达与患者年龄、肿瘤病理类型、国际妇产科协会(FIGO)分期均无相关性(均P>0.05),与肿瘤病理分化程度相关(χ2=2.694,P=0.005;χ2=2.284,P=0.018).pAkt1和hTERT蛋白同时阳性表达者无病生存期短于其他组患者(P=0.013).结论 pAkt1和hTERT蛋白同时高表达的EOC患者预后较差.%Objective To investigate the expression of phosphorylated protein kinase B1 (pAkt1) and human telomerase reverse transcriptase (hTERT) in ovarian epithelial carcinoma (EOC) and its relationship with prognosis, and to analyze the correlation between pAkt1 and hTERT expression. Methods 92 patients with EOC in Tangshan Gongren Hospital from January 2012 to December 2016 were selected. The expressions of hTERT and pAkt1 proteins were detected by immunohistochemistry. The relationship between the expressions of pAkt1 and hTERT proteins and their relationship with clinical prognosis were analyzed. Results Of the 92 patients with EOC, 68 cases (73.9 %) had positive expression of pAkt and 52 cases (56.5 %) had positive expression of hTERT. There was no significant correlation between expressions of pAkt1 and hTERT proteins in EOC (r= 0.284, P= 0.633). The expressions of pAkt1 and hTERT proteins were not related with age, tumor pathology type and the International Federation of Gynecology and Obstetrics (FIGO) staging (all P> 0.05), but had significant association with tumor pathology differentiation (χ2= 2.694, P= 0.005; χ2=2.284, P=0.018). The disease-free survival of patients with both pAkt1 and hTERT positive was shorter than that of the other groups (P= 0.013). Conclusion The prognosis of EOC patients with high expression of pAkt1 and hTERT proteins is poor.
    • 加秋萍; 贺清波
    • 摘要: 目的 评估液基细胞学检验(TCT)、人乳头状瘤病毒(HPV)、c-MYC、人染色体端粒酶RNA基因(hTERC)联合检测在宫颈癌筛查中的应用价值.方法 将本院妇科门诊接受检查的230例有性生活史的女性作为研究对象,分别进行TCT、HPV检测,并利用荧光原位杂交(FISH)法检测c-MYC、hTERC基因扩增情况,以病理组织学结果为金标准,分别比较四者单独及联合检测时对宫颈上皮内瘤变(CIN)Ⅱ/Ⅲ级及鳞状细胞癌(SCC)的敏感度、特异度、准确性.结果 230例筛查者中,TCT检测阳性124例,HPV阳性155例,c-MYC基因扩增118例,hTERC基因扩增128例.当TCT、HPV、c-MYC、hTERC单独使用时,HPV的敏感度最高(84.5%),c-MYC的特异度最高(97.6%);hTERC的准确性最高(85.2%).当两两组合时,TCT+ HPV与HPV+ hTERC的敏感度最高(均为89.2%),TCT+ hTERC的特异度最高(87.8%),c-MYC+ hTERC的准确性最高(86.5%).当三种指标任意配合使用时,TCT+ HPV+ hTERC的敏感度及准确性最高(98.6%、90.9%),TCT+ c-MYC+hTERC的特异度最高(79.3%).而四种指标联合使用时,敏感度为98.6%,特异度为72.0%,准确性为89.1%.结论 联合检查能提高宫颈病变筛查的敏感度和准确性,其中TCT+ HPV+ hTERC三者联合检查时诊断效率最佳,c-MYC基因检测具有最高的特异度.%Objective To investigate the application value of combination of thinprep cytologic test (TCT),human papilloma virus (HPV),c-MYC and human chromosome telomerase gene (hTERC) genes to screen cervical cancer.Methods A total of 230 cases of the study objects was detected with TCT and HP,respectively.Amplification of c-MYC and hTERC genes was tested with fluorescence in situ hybridization (FISH) method.The histopathological results were the gold standard,and the sensitivity,specificity and accuracy of cervical intraepithelial neoplasia (CIN) Ⅱ / Ⅲ and squamous cell carcinoma (SCC) were compared with the four combined detection.Results Of 230 screened patients,there were 124 cases of TCT positive,155 cases of HPV positive,c-MYC gene amplified in 118 cases,and hTERC gene amplified in 128 cases.When TCT,HPV,c-MYC,and hTERC were used alone,the highest sensitivity was HPV (84.5%),the highest specificity was c-MYC (97.6%),and the highest accuracy was hTERC (85.2%).When the three indexes were used in coordination with each other,the sensitivity and accuracy of TCT + HPV + hTERC were the highest (98.6% and 90.9%),and the specificity of TCT + c-MYC + hTERC was the highest (79.3%).When the four indexes were used together,the sensitivity was 98.6%,the specificity was 72.0%,and the accuracy was 89.1%.Conclusions Combined examination can improve the sensitivity and accuracy of screening cervical lesions,and the three combination of TCT + HPV + hTERC had the best effect,and c-MYC gene detection had the highest specificity.
    • 高晓东; 杨丽霞; 李永新; 苗海东
    • 摘要: 目的:探讨hTERT基因全硫代修饰反义寡核苷酸(AS PS-ODN)抑制氟他胺耐受型前列腺癌细胞LNCaP-flu端粒酶活性后,藏药镰状棘豆总黄体酮(TFOF)对LNCaP-flu细胞凋亡的影响。方法采用TRAP-PCR-ELISA法检测氟他胺耐受型前列腺癌细胞LNCaP-flu端粒酶活性;采用台盼蓝观察hTERT AS PS-ODN与TFOF共同作用对氟他胺耐受型前列腺癌细胞LNCaP-flu生长活力的影响;通过双标流式细胞仪测定凋亡细胞的百分率。结果hTERT AS PS-ODN作用于LNCaP-flu细胞48h,端粒酶活性明显下降;hTERT AS PS-ODN作用于LNCaP-flu细胞后加入TFOF 0.1g/L作用48h,LNCaP-flu细胞的抑制率与对照组、S PS-ODN组、AS PS-ODN组、TFOF组及S PS-ODN+TFOF组相比有统计学差异(P<0.01)。hTERT AS PS-ODN作用于LNCaP-flu细胞后加入0.1g/L TFOF作用48h,凋亡细胞的百分率分别与对照组、S PS-ODN组、AS PS-ODN组、TFOF组及S PS-ODN+TFOF组相比有显著性差异(P<0.05)。结论 hTERT基因反义核酸对TFOF诱导的氟他胺耐受型前列腺癌细胞LNCaP-flu凋亡有增敏作用。%Objective To investigate the effects of telomerase inhibition with hTERT antisense on oxytropis falcata (TFOF)-induced apoptosis in flutamide insensitive prostate cancer cells (LNCaP-flu). Methods Antisense phosphorothioate oligodeoxynucleotide (AS PS-ODN) was synthesized and purified. Telomerase activity was measured by telomerase PCR ELISA kit. Cell viability was determined by MTT assay;Cell apoptosis was determined by flowcytometry. Results AS PS-ODN significantly inhibited telomerase activity. The cell viability decreased with time after hTERT AS PS-ODN combined with TFOF treatment. The percentage of apoptosis increased with time after hTERT AS PS-ODN combined with TFOF treatment. There was no difference in cell viability and the percentage of apoptosis between S PS-ODN and the control group.. Conclusion Inhibition of telomerase with hTERT antisense can enhance TFOF-induced apoptosis in flutamide insensitive prostate cancer cells (LNCaP-flu).
    • 吕永昌
    • 摘要: 端粒、端粒酶在肿瘤的发生发展及结局中扮演着重要的角色,尤其是端粒酶启动子区域的突变对肿瘤影响至关重要,在大部分肿瘤中能检测到该区域的突变.膀胱癌是泌尿系统最常见的恶性肿瘤之一,本文旨在总结现阶段端粒、端粒酶与膀胱癌之间关系的研究现状.
    • 郑浩; 李占鲁; 孔旭钢; 沈啸华; 傅国胜
    • 摘要: 目的:观察香烟烟雾提取物(CSE)对外周血内皮祖细胞(EPC)衰老的影响,探讨其可能机制。方法密度梯度离心法获取人外周血单核细胞,培养4d 后,收集贴壁细胞,分别加入2.5%,5%,10%和15%的 CSE 干预。采用SA β半乳糖苷酶染色试剂盒检测衰老细胞;MTT 比色法检测 EPC 的增殖能力;端粒重复序列扩增法(TRAP) ELISA 定量检测 EPC 端粒末端转移酶活性;逆转录 PCR 法检测人端粒酶逆转录因子(human telomerase reverse transcriptase , hTERT)mRNA 水平;Western 蛋白印迹检测 EPC Akt Ser473磷酸化水平。结果 CSE 能显著增加 SA β半乳糖苷酶阳性细胞数量,15% CSE 影响最为明显,同时显著抑制 EPC 增殖能力;CSE 能显著抑制端粒酶活性及 hTERT mRNA 表达;另外,CSE 能抑制 EPC Akt 磷酸化。结论 CSE 诱导 EPC 衰老,伴随 EPC 增殖能力的损害,提示细胞衰老也许是 CSE 影响 EPC 功能的机制之一;CSE 诱导 EPC 衰老可能与抑制 EPC 端粒末端转移酶活性、减少 hTERT mRNA 表达及抑制 Akt磷酸化有关。%Objective To investigate whether cigarette smoke extract (CSE) might be able to accelerate the onset of endothelial pro-genitor cell (EPC) senescence as well as its underlying mechanisms. Methods Total mononuclear cells (MNCs) were isolated from peripheral blood by density gradient centrifugation ,and then the cells were plated on fibronectin coated culture dishes. After 4 days , adherent cells were collected and treated with 2.5 ,5 ,10 and 15% CSE respectively. Senescence associated β galactosidase (SA βGal) staining kit was utilized to monitor EPC senescence. The proliferation of EPC was assessed by 3 (4 ,5 dimethylthiazol 2 yl) 2 , 5 diphenyltetrazolium bromide (MTT) assay. Telomerase activity was measured by quantitative analysis of telomeric repeat amplifica-tion protocol (TRAP) ELISA in EPC. The mRNA levels of human telomerase reverse transcriptase (hTERT) were measured by re-verse transcription polymerase chain reaction (PCR). Phosphorylation of EPC Akt Ser473 was detected by Western blot. Results CSE significantly increased the number of SA β Gal positive cells. It reached to the maximum at 15% (14.17 ± 5.42 vs 55.50 ± 9.40). Moreover ,CSE significantly decreased EPC proliferation (0.22 ± 0.04 vs 0.04 ± 0.01). CSE down regulated the expression of hTERT mRNA in a concentration dependent manner ,with a maximal decrease in 15% . CSE also significantly decreased telom-erase activity (0.44 ± 0.09 vs 0.21 ± 0.06). In addition ,CSE treatment of EPC concentration dependently diminished Akt phospho-rylation. Conclusions CSE induced EPC senescence with the damage to the proliferation of EPC. This indicates that cellular senes-cence may be one of the mechanisms by which CSE affects EPC function. CSE induced EPC senescence could be associated with the inhibition of EPC telomerase activity ,the decrease of mRNA hTERT expression and the inhibition of Akt phosphorylation.
    • 宋妮娜; 瞿全新
    • 摘要: 宫颈癌是妇科最常见的恶性肿瘤之一,近年来宫颈癌的发病率逐年上升,且有年轻化趋势。宫颈上皮内瘤变(CIN)是由高危型人乳头瘤病毒(HPV)的持续性感染引起的,是宫颈癌的癌前病变,其反映宫颈癌发生发展中的连续过程,从CIN发展为宫颈癌需要较长的时间。在CIN的进展过程中,许多基因结构和功能都会发生变化。近年来的研究发现,在CIN和宫颈癌的组织中存在着一些表达异常的生物学标记物,这些生物学标记物与前驱病变级别和肿瘤是否发生转移相关,将这些基因作为CIN进展的分子生物学标志物进行检测,早期发现和诊断宫颈癌已成为目前研究的热点。综述CIN研究的前沿性分子生物学指标。%Cervical cancer is one of the most common gynecological malignant tumors. In recent years, the incidence of cervical cancer has increased year by year, and there is a trend of youth. Cervical intraepithelial neoplasia (CIN) is caused by persistent infection of high risk human papillomavirus (HPV). It is a precancerous lesion of cervical cancer, and it reflects the continuous process of the development of cervical cancer. From the development of CIN to cervical cancer needs a long time. In the progress of CIN, many gene structure and function will change. Recent studies have found that there are some abnormal expression of biological markers between the CIN and cervical cancer tissue, which are related to the level of the precursor and the metastasis of the tumor. These genes as CIN progression of molecular biomarkers for testing to early detect and diagnosis of cervical cancer has become a hot research. In this article, we reviewed the research on the frontier molecular biology of CIN.
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