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人乳头瘤病毒16型

人乳头瘤病毒16型的相关文献在1996年到2022年内共计134篇,主要集中在基础医学、肿瘤学、分子生物学 等领域,其中期刊论文131篇、会议论文3篇、专利文献975519篇;相关期刊81种,包括生物化学与生物物理进展、微生物学杂志、中华流行病学杂志等; 相关会议3种,包括2014年山东省科协学术年会、第七次全国医学分子微生物学及生物技术研讨会、中国微生物学会基础与临床病毒学会议等;人乳头瘤病毒16型的相关文献由438位作者贡献,包括谷鸿喜、商庆龙、魏兰兰等。

人乳头瘤病毒16型—发文量

期刊论文>

论文:131 占比:0.01%

会议论文>

论文:3 占比:0.00%

专利文献>

论文:975519 占比:99.99%

总计:975653篇

人乳头瘤病毒16型—发文趋势图

人乳头瘤病毒16型

-研究学者

  • 谷鸿喜
  • 商庆龙
  • 魏兰兰
  • 王燕
  • 千新来
  • 张菊
  • 李茉
  • 阎小君
  • 冶亚平
  • 常海敏
  • 期刊论文
  • 会议论文
  • 专利文献

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    • 李亚芹; 刘亚涛; 张宏蕾; 赵卫红
    • 摘要: 目的探讨微小RNA 203-3p(miR-203)靶向调控枯灵素2(CUL2)对人乳头瘤病毒16型(HPV16)阳性宫颈癌细胞生物学特性的影响。方法收集2018年9月-2019年9月于山西医科大学第二医院妇产科行宫颈癌筛查,HPV检测为单一HPV16阳性,病理检查为宫颈鳞癌(SCC)的样本及相应癌旁组织(对照组)各10份。采用实时定量反转录聚合酶链反应(qRT-PCR)检测SCC与相应癌旁组织,以及人SCC细胞(SiHa)与人永生化表皮细胞(HaCaT)中miR-203的表达。采用GO和KEGG富集法分析miR-203参与的功能和通路,TargetScan网站及双荧光素酶报告基因实验验证miR-203与CUL2的靶向调控作用。将miR-203模拟物或抑制剂转染至SiHa细胞,建立过表达或低表达miR-203的细胞模型,采用qRT-PCR和Western blotting检测CUL2 mRNA及蛋白的表达;采用CCK-8法、划痕实验、AnnexinⅤ-APC/PI双染色法评估SiHa细胞的增殖、迁移和凋亡能力。结果qRTPCR检测分析结果显示,与相应癌旁组织和HaCaT细胞相比,miR-203在SCC组织和SiHa细胞中的表达水平均明显降低(P<0.01)。GO和KEGG富集结果显示,miR-203广泛参与泛素化过程并与恶性肿瘤参与的信号通路有关。TargetScan与双荧光素酶报告基因实验表明,miR-203与CUL2存在靶向调控关系(P<0.01)。qRT-PCR及Western blotting结果表明,过表达miR-203时,CUL2 mRNA及蛋白表达水平均明显降低(P<0.05或P<0.01),而低表达miR-203则可上调CUL2 mRNA及蛋白的表达(P<0.01)。CCK-8、划痕实验和AnnexinⅤ-APC/PI双染结果显示,过表达miR-203可降低SiHa细胞的增殖率和迁移率(P<0.01),升高细胞凋亡率(P<0.05);相反,低表达miR-203可升高SiHa细胞的增殖率和迁移率(P<0.01),降低细胞凋亡率(P<0.01)。结论miR-203可能通过靶向CUL2抑制HPV16阳性宫颈癌细胞SiHa的生物学特性,有望成为宫颈癌诊断和治疗的一个新的候选基因。
    • 刘君; 马秀丽; 薛晓鸥
    • 摘要: 目的 研究外用中药清热除湿凝胶对人乳头瘤病毒(HPV)16阳性的宫颈癌荷瘤小鼠线粒体凋亡蛋白的影响.方法 培养HPV16阳性人宫颈癌SiHa细胞株,制成浓度为2×107/mL的细胞悬液.选取5周龄雌性裸小鼠,用1 mL注射器抽取充分混匀的细胞悬液,注入裸小鼠右前腿外上方皮下,造成HPV16阳性移植瘤模型.造模成功后采用随机数字表法将荷瘤小鼠分为5组,每组10只.即模型组、卡波姆940组、中药组、顺铂组及联合用药组.中药组于成瘤部位给予清热除湿凝胶外涂(每天每50 mm3瘤体体积外涂凝胶0.3 mL);顺铂组:将10 mg顺铂溶于66.7 mL生理盐水中制成顺铂注射液腹腔注射(每10 g体重注射0.2 mL,每3天注射1次);卡波姆940组(凝胶中辅料):卡波姆940外涂(每天每50 mm3体积外涂0.15 mL);联合用药组:同时给予中药外涂和顺铂腹腔注射,各组共给药28 d.而后麻醉剥取小鼠右前腿肿瘤组织,免疫荧光法进行检测细胞凋亡,同时Western blot法检测组织中凋亡相关蛋白Bax、Bcl-2、Caspase-9、Caspase-3.结果 与模型组、卡波姆940组比较,中药组、顺铂组、联合用药组细胞凋亡率均有升高,以联合用药凋亡率最高,差异有统计学意义(P0.05).与模型组、卡波姆940组比较,中药组、顺铂组、联合用药组Bax、Caspase-3表达均上调,Bcl-2表达均下降,且联合用药组表达最明显,差异有统计学意义(P<0.05).与模型组、卡波姆940组比较,顺铂组、联合用药组Caspase-9表达上调,差异有统计学意义(P<0.05).结论 清热除湿凝胶能改变HPV16阳性的宫颈癌荷瘤小鼠的细胞凋亡,该外用药发挥抗毒抑瘤作用的机制可能与上调肿瘤组织线粒体凋亡相关蛋白Bax、Caspase-9、Caspase-3,下调Bcl-2有关.
    • 周爱枝; 段迎春; 张蕾; 戴晓莉; 杨玉梅; 任青
    • 摘要: 目的 探讨雌激素、雌激素受体及白介素-17(IL-17)在人乳头瘤病毒(HPV)感染与清除过程中的作用.方法 选取上海市浦东新区人民医院2014年8月至2017年1月门诊或住院部宫颈细胞学正常、HPV阴性或单一人乳头瘤病毒16型(HPV16)阳性的患者,采用宫颈TCT对所有研究对象进行细胞学检测,反向斑点杂交技术进行HPV亚型分析及实时荧光PCR进行HPV16 DNA定量;用酶联免疫吸附试验(ELISA)方法检测血清中雌激素(E2)水平及宫颈灌洗液中IL-17浓度,免疫组化检测雌激素受体(ER)表达水平.上述实验每3个月重复一次.按照HPV16感染结局的不同,将实验分为HPV阴性组、HPV16清除组和HPV16持续感染组.结果 将所有研究对象最后一次检查结果与第一次检查结果对比发现,HPV阴性组、HPV16清除组及HPV16持续感染组之间E2比较,差异无统计学意义(P>0.05),ER在各组之间的差异也不明显,差异均无统计学意义(P>0.05).IL-17表达浓度差在HPV阴性组与HPV16持续感染组间差异无统计学意义,二者与HPV16清除组之间IL-17浓度差异显著,HPV16清除组中IL-17浓度明显增高.结论 在细胞学正常,而仅为HPV16感染阶段,内源性E2及宫颈局部组织中的ER可能并没有发挥作用,抑或E2或ER对HPV感染影响不大,而局部免疫因子IL-17在HPV16清除过程中发挥了重要作用,IL-17浓度的增加有利于HPV16的清除.%Objective To understand the role of estrogen,estrogen receptor and IL-17 in human papillomavirus (HPV) infection and clearance.Methods We selected the clinic or the hospitalized patients in People' s Hospital of Pudong New District hospital with HPV negative or single-HPV16 positive during the period of August 2014 to January 2017.Cervical exfoliated cells were harvested by Thinprep cytologic test (TCT).The reverse spot hybridization technique was carried out for HPV subtype analysis.RT-PCR was employed for HPV16 DNA viral load.The levels of E2 and IL-17 were detected by ELISA.Immunohistochemical was used to detect ER expression.The experiments were repeated every three months.According to the difference in the outcome of human papilloma virus 16 infection,the experiment was divided into three groups.The first group was HPV negative,which was negative for one year.The second group was HPV16 positive,but within one year the difference was gradually cleared.The third group was HPV16 positive,but the HPV16 persistently existed after one year.Results The results of the last test were compared with the first test results.We found that There was no significant difference among the three groups in the expression of E2 and ER.Also,there was no significant difference between the HPV negative group and the HPV16 persistently infected group in variation of IL-17 concentration.But the difference between the HPV16 cleared group and the anyone of the two groups above was significantly.The variation of IL-17 concentration was significantly higher in the HPV16 cleared group.Conclusion In normal cytology,and only HPV16 infected stage,endogenous E2 and ER of cervix may not play a role in HPV infection,or they may have little effect on HPV infection.Local immune factor IL-17 plays an important role in the process of HPV16 removal,and the increase of IL-17 concentration can help to eliminate HPV16.
    • 崔玉伟; 牟颖; 马莉; 丁雄; 方宗宇; 王焰; 吴青青
    • 摘要: 应用等温多自配引发扩增(IMSA)技术,分别针对人乳头瘤病毒(HPV)16型的E7和52型的E6基因序列设计6条特异性引物,并在检测体系中加入羟基萘酚蓝(HNB)和SYBR GreenⅠ的混合双荧光指示剂,建立快速检测人乳头瘤病毒的双荧光IM SA方法.结果表明:340μmol/L HNB与1:10000 SYBR GreenⅠ混合构建的双荧光指示剂在IMSA反应体系中具有明确的指示效果,455 n m蓝光激发下阳性反应管双荧光显色为黄绿色,阴性反应管双荧光显色为橘红色;该方法对HPV16和HPV52型检测限分别达60,600拷贝/μL,可特异性检出样品中HPV16和HPV52,与临床检测结果比对无差异.
    • 丁玲; 王金桃; 冯美娟; 刘春亮; 王璐; 宋志超; 杨倩; 李小雪; 宋丽; 高雯
    • 摘要: 目的 探讨hnRNPK与HPV16感染在宫颈上皮内瘤样变(CIN)中的作用及其交互效应.方法 选取2014年6月至2015年6月在山西省介休市建立的社区队列中经病理学确诊的正常宫颈(NC)女性67例和CIN患者137例(CIN Ⅰ患者69例、CINⅡ/Ⅲ患者68例)为研究对象.采用结构式问卷收集研究对象人口学资料及宫颈病变相关因素的基础上,采集宫颈脱落细胞和宫颈活检或手术组织,应用分子导流杂交法检测HPV16感染状况,并采用Western blot技术检测宫颈组织中hnRNPK蛋白表达水平.采用SPSS 23.0软件对资料进行整理分析,研究对象的人口学特征、相关因素、hnRNPK蛋白和HPV16感染在NC组、CIN Ⅰ和CINⅡ/Ⅲ组的差异通过x2检验、趋势x2检验、Kruskal-Wallis H检验进行比较;hnRNPK蛋白表达量的组间两两多重比较采用Bonferroni法;采用非条件logistic回归模型计算hnRNPK蛋白、HPV16感染与CIN的关联强度OR值及其95%CI,采用相加交互模型及交互效应指标评价hnRNP K蛋白和HPV16感染两因素在CIN中的交互效应.结果 CINⅡ/Ⅲ组HPV16感染率(41.2%)高于NC(10.4%)、CIN Ⅰ (14.5%),差异有统计学意义(P<0.001),且随着CIN程度加重,HPV16的感染率呈上升趋势(趋势x2=18.512).hnRNPK蛋白表达量在NC组、CIN Ⅰ组和CINⅡ/Ⅲ组间差异有统计学意义(H=48.138,P<0.001),且随着C1N程度加重呈上升趋势(趋势x2=21.765,P<0.001).交互效应分析显示,hnRNPK蛋白高表达与HPV16感染在CINⅡ/Ⅲ组存在正相加交互作用(API=0.639,95%CI:0.083~1.196),在CIN Ⅰ组尚未发现存在类似交互作用.结论 hnRNP K蛋白高表达、HPV16感染均可能增加CIN的发生风险,且在高度CIN发生中存在正相加交互作用.%Objective To investigate the effect of heterogeneous nuclear ribonucleoprotein K (hnRNP K) and its interaction with human papillomavims 16 (HPV16) on cervical intraepithelial neoplasia (CIN).Methods The participants included 67 women with normal cervix (NC),69 women with CIN Ⅰ and 68 women with CIN Ⅱ/Ⅲ in a community cohort of pathologically diagnosed women established in Jiexiu of Shanxi province,from June 2014 to June 2015.A structured questionnaire was used to collect the demographic data of the subjects and the related factors of cervical lesions.Cervical exfoliated cells and cervical tissues from biopsy or surgery were selected.The infection status of HPV16 was detected by flow-through hybridization.The protein expression levels of hnRNP K were evaluated by Western blot.SPSS 23.0 software was used to collate and analyze the data.To study the differences in demographic characteristics,related factors,hnRNP K protein and HPV16 infection among NC,CIN Ⅰ and CIN Ⅱ / Ⅲ groups,X2 test,trend x2 test,and Kruskal-Wallis H test were conducted.Multiple comparisons of hnRNP K protein in three groups were completed by using the Bonferroni method.The OR and its 95%CI of hnRNP K,HPV16 and CIN were calculated by using the unconditional logistic regression models.Two-way interactions between hnRNP K protein and HPV16 infection on CIN were analyzed by using additive model and related indicators.Results HPV16 infection rates were 10.4% in women with normal cervix,14.5% in women with CIN Ⅰ and 41.2% in women with CIN Ⅱ/Ⅲ,respectively.The differences among three groups were significant (P<0.001).Moreover,the infection rates of HPV16 gradually increased with the increasing severity of CIN (trend x2=18.512,P<0.001).The differences in protein expression of hnRNP K among three groups were significant (H=48.138,P<0.001) and the expressionincreased with the development of cervical lesionss (trend x2=21.765,P<0.001).Results from the interaction analysis indicated that there were additive effects between high expression of hnRNP K protein and HPV16 in CIN Ⅱ/Ⅲ group compared with normal group (API=0.639,95%CI:0.083-1.196).In contrast,no such additive effect was found in CIN Ⅰ group.Conclusions HPV16 infection and over-expression of hnRNP K protein were associated with the increased risk of cervical intraepithelial neoplasia.There might be interaction between hnRNP K protein overexpression and HPV16 infection existed on the progress of CIN Ⅰ/Ⅲ.
    • 颜学勤; 王莹莹; 嵩钰佳; 王鑫; 陈思佳; 魏兰兰; 钟照华; 商庆龙
    • 摘要: 目的 建立人乳头瘤病毒(human papillomavirus,HPV)16型E7蛋白的原核表达系统,表达HPV16 E7蛋白,制备小鼠抗HPV16 E7血清.方法 采用PCR方法扩增HPV16 E7基因,构建入pET21b质粒,重组表达载体经鉴定后转化大肠埃希菌BL21(DE3).诱导表达后经十二烷基硫酸钠(so-dium dodecyl sulphate,SDS)-聚丙烯酰胺凝胶电泳(polyacrylamide gel electrophoresis,PAGE)和Western blot鉴定表达产物.提取包涵体进行变性复性处理后纯化,纯化后的可溶性蛋白免疫Balb/C小鼠,检测小鼠体内 γ-干扰素(interferon-γ,IFN-γ)水平、CD4/CD8比值和抗血清滴度变化.结果 PCR扩增片段为0.3 Kb,酶切和序列测定证实重组质粒构建正确.SDS-PAGE在11 KD处出现蛋白条带.蛋白表达以包涵体为主.免疫后小鼠抗体效价升高,CD4/CD8比值无升高,IFN-γ无反应.结论 成功制备可溶性HPV16E7蛋白和小鼠抗HPV16E7高效价抗血清.
    • 胡天; 卓永光; 樊祖茜; 黄永霞
    • 摘要: 目的建立一种可准确、快速检测沙眼衣原体、单纯疱疹病毒2型、人乳头瘤病毒16型3种病原体DNA的多重荧光定量PCR检测方法。方法本研究针对沙眼衣原体、单纯疱疹病毒2型、人乳头瘤病毒16型分别设计了一对特异性探针引物,构建了可同时检测沙眼衣原体、单纯疱疹病毒2型、人乳头瘤病毒16型的多重荧光PCR反应体系,并与商业试剂同时检测300例临床标本,评估其一致性。结果性能评价结果显示,所建立的多重荧光PCR检测方法具有较好的特异性和敏感性,与对照商业试剂检查结果符合率达到100%。结论所建立的多重荧光PCR检测方法能实现3种病原体的快速、正确定量检测。
    • 宋丹; 史茜; 侯向前; 玛依努尔·尼亚孜; 马正海
    • 摘要: Background and purpose:The incidence of cervical cancer is rather high in Xinjiang, which is closely associated with the infection of human papilloma virus type 16 (HPV-16). The purpose of this study was to analyze the variants and function of HPV-16 upstream regulatory region (URR) in the tissues of cervical cancer biopsies from Xinjiang.Methods:The DNAs were extracted from the tissues of cervical epithelial atypical hyperplasia (CIN) and cervical cancer biopsies. HPV-16URR segments were ampliifed by PCR. Based on the sequence analysis of the URR, the representativeURR variants were selected and cloned into pGL3-Basic. The recombinant plasmids were transfected into Vero cell lines respetively. Luciferase activity of transfected cells was detected 48 h after transfection. Results:Fifty-ifve HPV-16URR DNA fragments were obtained through PCR, and 44 mutations were found from the URR fragments. 4 of these mutations, including nt7192(G→T) , nt7433(- →T), nt7435 (C→G) and nt7863 (A→-) occurred in all sequences. The mutation at nt7520 (G→A) occurred in 54URR sequences, and the 39 other mutations were present in different samples. Based on the location and frequency of the mutations in theURR fragments, 9URR variants were selected and cloned into pGL3-Basic. Then the luciferase activity of the cells transfected with pGL3-URR plasmids was detected respectively. Promoter activity ofURR mutants from cervical cancer are significantly higher than that ofURR mutants from CIN (P<0.01). Promoter activity ofURR fragments from some cervical cancer was signiifcantly higher than that of theURR fragments from SiHa and Caski cells.Conclusion:Multiple mutations occurred in HPV-16URR of cervical cancer patients from Xinjiang. The promoter activity and carcinogenicity of some URR mutants have been enhanced.%背景与目的:新疆是宫颈癌高发区,该地区宫颈癌高发与人乳头瘤病毒16型(human papillomavirus type 16,HPV-16)感染密切相关.该研究旨在分析新疆地区妇女宫颈病样组织中HPV-16上游调控区(upstream regulatory region,URR)的突变及其功能.方法:以新疆妇女子宫颈上皮非典型增生(cervical intraepithelial neoplasia,CIN)和宫颈癌病样组织标本DNA为模板,PCR扩增HPV-16URR片段,PCR产物经测序比对,筛选代表性的URR突变体构建至pGL3-Basic载体,将其转染Vero细胞,48 h后检测荧光素酶活性,分析URR突变体启动子活性.结果:采用聚合酶链反应(polymerase chain reaction,PCR)获得了55个HPV-16URR DNA片段,测序及序列分析发现44个突变位点,其中nt7192(G→T)、nt7433(-→T)、nt7435(C→G)和nt7863(A→-)4个位点的突变为所有序列共有,nt7520(G→A)位点的突变存在于54个样品中,剩余39个位点的突变存在于不同样品中.根据突变的位置、频率和程度,筛选出9个URR突变体分别克隆至pGL3-Basic中荧光素酶基因前并转染Vero细胞.荧光素酶活性分析表明,不同URR突变体的启动子活性差异较大,来源于宫颈癌的URR突变体启动子活性显著高于来源于CIN的URR突变体(P<0.01),部分宫颈癌URR突变体的启动子活性显著高于SiHa和Caski细胞来源的URR参照序列的启动子活性.结论:新疆地区分离的HPV-16 URR发生多位点突变,其中部分突变增强了URR内部启动子的活性,导致HPV-16致癌活性增强.
    • 李会影; 王慧智; 张子旸
    • 摘要: 目的:探讨miR-27a-3p和同源盒B8(HOXB8)蛋白在人乳头瘤病毒16型阳性[HPV16(+)]和阴性[HPV16(-)]患者宫颈癌组织中表达的差异及其机制.方法:选取2012年1月-2016年1月于我院就诊的宫颈癌患者120例,根据其是否感染HPV16分为HPV16(+)组(60例)和HPV16(-)组(60例).采用实时荧光定量聚合酶链反应法检测两组患者宫颈癌组织中miR-27a-3p和HOXB8 mRNA的表达水平,采用蛋白印迹法检测HOXB8蛋白的表达水平,采用巢式降落式甲基化特异性聚合酶链反应法检测miR-27a-3p启动子区DNA甲基化水平,采用染色质免疫共沉淀-定量聚合酶链反应法检测miR-27a-3p启动子区组蛋白甲基化水平;培养人宫颈癌细胞系SiHa细胞株,考察转染miR-27a-3p模拟物(mimic)和抑制物(inhibitor)后miR-27a-3p和HOXB8 mRNA的表达水平.结果:HPV16(+)组患者宫颈癌组织中miR-27a-3p的表达水平显著低于HPV16(-)组患者,HOXB8 mRNA和蛋白表达水平、miR-27a-3p启动子区DNA甲基化水平和组蛋白甲基化水平均显著高于HPV16(-)组患者,差异均有统计学意义(P<0.05或P<0.01).在SiHa细胞转染miR-27a-3p mimic后,miR-27a-3p的表达水平显著升高,而HOXB8 mRNA的表达水平显著降低;转染miR-27a-3p inhibitor后,miR-27a-3p的表达水平显著降低,而HOXB8 mRNA的表达水平则显著升高,差异均有统计学意义(P<0.01).结论:HPV16可能通过启动子区DNA甲基化和组蛋白甲基化下调miR-27a-3p的表达,从而影响宫颈癌的发生与发展,HOXB8蛋白可能是其作用靶点.%OBJECTIVE:To investigate the expression difference and its mechanism of miR-27a-3p and HOXB8 protein in cer-vical cancer tissues of HPV16-positive and HPV16-negative patients. METHODS:A total of 120 patients with cervical cancer in our hospital during Jan. 2012-Jan. 2016 were divided into HPV16-positive group(60 cases)and HPV16-negative group(60 cases) according to HPV16 infection situation. The expression of miR-27a-3p mRNA and HOXB8 mRNA in cervical cancer tissue were de-tected by RT-qPCR. The expression of HOXB8 protein was detected by Western blotting assay. DNA methylation level of miR-27a-3p promoter region was detected by nested-down methylation specific PCR (nMS-PCR). Histone methylation level of miR-27a-3p promoter region was detected by chromatin immunoprecipitation PCR (CHIP-PCR). The expression of miR-27a-3p mRNA and HOXB8 mRNA were detected after transfecting miR-27a-3p mimic and inhibitor into Human cervical cancer cell line SiHa,respectively. RESULTS:The expression of miR-27a-3p in HPV16-positive group was significantly lower than HPV16-nega-tive group,while HOXB8 mRNA and protein expression,DNA and histone methylation levels of miR-27a-3p promoter region were significantly higher than HPV16-negative group,with statistical significance (P<0.05 or P<0.01). After transfecting miR-27a-3p mimic into SiHa cells,the expression of miR-27a-3p was increased significantly,while that of HOXB8 mRNA was de-creased significantly;after miR-27a-3p inhibitor transfection,the expression of miR-27a-3p was decreased significantly,while that of HOXB8 mRNA was increased significantly,with statistical significance(P<0.01). CONCLUSIONS:HPV16 may down-regu-late the expression of miR-27a-3p through DNA methylation and histone methylation of promoter region,so as to influence the gen-eration and development of cervical cancer. HOXB8 may be the target protein of miR-27a-3p.
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