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A homeodomain-leucine zipper I transcription factor, MeHDZ14,regulates internode elongation and leaf rolling in cassava(Manihot esculenta Crantz) 被引量:4
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作者 Xiaoling Yu Xin Guo +6 位作者 Pingjuan Zhao Shuxia Li Liangping Zou Wenbin Li Ziyin Xu Ming Peng Mengbin Ruan 《The Crop Journal》 SCIE CSCD 2023年第5期1419-1430,共12页
Drought stress impairs plant growth and other physiological functions. MeHDZ14, a homeodomainleucine zipper I transcription factor, is strongly induced by drought stress in various cassava cultivars.However, the role ... Drought stress impairs plant growth and other physiological functions. MeHDZ14, a homeodomainleucine zipper I transcription factor, is strongly induced by drought stress in various cassava cultivars.However, the role of MeHDZ14 in cassava growth regulation has remained unclear. Here we report that MeHDZ14 affected plant height, such that a dwarf phenotype and altered internode elongation were observed in transgenic cassava lines. MeHDZ14 was found to negatively regulate the biosynthesis of lignin. Its overexpression resulted in abaxially rolled leaves. The morphogenesis of leaf epidermal cells was inhibited by overexpression of MeHDZ14, with decreased auxin and gibberellin and increased cytokinin contents. MeHDZ14 was found to regulate many drought-responsive genes, including genes involved in cell wall synthesis and expansion. MeHDZ14 bound to the promoter of caffeic acid 3-Omethyltransferase 1(MeCOMT1), acting as a transcriptional repressor of genes involved in cell wall development. MeHDZ14 appears to act as a negative regulator of internode elongation and epidermal cell morphogenesis during cassava leaf development. 展开更多
关键词 hd-zip transcription factor DROUGHT Internode elongation Leaf rolling CASSAVA
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维甲酸对转化生长因子β1诱导的HFL-I细胞Ⅲ型胶原、STAT3和PIAS3表达的影响 被引量:2
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作者 夏武 杨宇平 +2 位作者 陈永凤 程娜 刘巨源 《中国病理生理杂志》 CAS CSCD 北大核心 2012年第6期1114-1119,共6页
目的:研究全反式维甲酸(ATRA)对转化生长因子β1(TGF-β1)诱导的人胚肺成纤维细胞(HFL-I)中Ⅲ型胶原(collagenⅢ)、信号转导子和转录激活子3(STAT3)和活化STAT3蛋白抑制剂(PIAS3)表达的影响。方法:体外培养HFL-I细胞,5μg/L TGF-β1诱导... 目的:研究全反式维甲酸(ATRA)对转化生长因子β1(TGF-β1)诱导的人胚肺成纤维细胞(HFL-I)中Ⅲ型胶原(collagenⅢ)、信号转导子和转录激活子3(STAT3)和活化STAT3蛋白抑制剂(PIAS3)表达的影响。方法:体外培养HFL-I细胞,5μg/L TGF-β1诱导0 h、6 h、12 h、24 h、48 h和72 h后,RT-PCR法检测colla-genⅢ、STAT3和PIAS3 mRNA表达,诱导0 d、1 d、3 d和5 d后,Western blotting法检测STAT3和p-STAT3蛋白表达。不同浓度维甲酸干预,24 h后用RT-PCR法检测collagenⅢ、STAT3和PIAS3 mRNA表达,3 d后用Westernblotting法检测STAT3和p-STAT3蛋白表达。结果:TGF-β1诱导后,HFL-I细胞中collagenⅢ和STAT3 mRNA表达明显上调,PIAS3 mRNA表达明显下调,STAT3和p-STAT3蛋白表达明显上调(P<0.05)。各浓度ATRA都下调TGF-β1诱导的HFL-I细胞中collagenⅢ、STAT3 mRNA和STAT3、p-STAT3蛋白的表达,上调PIAS3 mR-NA表达(P<0.05)。结论:ATRA可通过抑制TGF-β1诱导的HFL-I细胞collagenⅢ和STAT3表达、上调PIAS3表达而起到抗肺纤维化作用。 展开更多
关键词 转化生长因子Β 全反式维甲酸 胶原 信号转导子和转录激活子3 活化STAT3蛋白抑制剂
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筛选甘蔗SPSⅢ启动子诱饵片段结合蛋白的酵母单杂交诱饵质粒的构建 被引量:2
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作者 邹丽娟 高玉娜 +3 位作者 周平 叶冰莹 陈由强 陈如凯 《福建师范大学学报(自然科学版)》 CAS CSCD 北大核心 2011年第1期76-79,共4页
主要构建了可以与酵母染色体发生重组的质粒pAbAI-Bait,并转化大肠杆菌DH5α感受态细胞获得转化子,将阳性克隆进行PCR与DNA测序的方法鉴定,结果表明:酵母单杂交中报告质粒pAbAI-Bait构建成功,可用于酵母单杂交体系.
关键词 酵母单杂交 蔗糖磷酸合成酶基因 转录因子
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针对SP1的圈套寡脱氧核苷酸抑制NIH_3T_3细胞活力和Ⅲα_1胶原基因表达的研究
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作者 张世新 杨松林 +3 位作者 万伟东 史毅 邓辰亮 金由辛 《中国美容医学》 CAS 2008年第2期217-221,共5页
目的:研究针对转录因子SP1的圈套寡脱氧核苷酸(Decoy-Oligodeoxynucleotide,Decoy-ODN)对小鼠胚胎成纤维细胞(NIH3T3)的活力和Ⅲα1胶原基因表达的影响,探讨圈套寡脱氧核苷酸用于病理性瘢痕基因治疗的可能性及机理。方法:设计合成针对SP... 目的:研究针对转录因子SP1的圈套寡脱氧核苷酸(Decoy-Oligodeoxynucleotide,Decoy-ODN)对小鼠胚胎成纤维细胞(NIH3T3)的活力和Ⅲα1胶原基因表达的影响,探讨圈套寡脱氧核苷酸用于病理性瘢痕基因治疗的可能性及机理。方法:设计合成针对SP1的特异性哑铃形Decoy-ODN。用阳离子脂质体转染NIH3T3细胞。分别用流式细胞仪检测ODN转染效率,激光共聚焦显微镜观察ODN在细胞中的分布,电泳迁移率变动分析(electrophoretic mobility shift assay,EMSA)验证ODN与SP1的特异性结合。用WST-8检测ODN对细胞活力的影响。用RT-PCR检测ODN对细胞胶原基因表达的抑制作用。结果:分别转染25nM、50nM、100nM、150nM SP1 Decoy-ODN,48h后,细胞活力依次为0.9331±0.0203、0.7479±0.0868、0.577±0.0347、0.4703±0.0147;转染100nMSP1Decoy-ODN可明显抑制Ⅲα1胶原mRNA的表达(P<0.01),抑制效果达60%。结论:Decoy-ODN可以通过拮抗核转录因子SP1的活性而抑制NIH3T3细胞的活力和Ⅲα1胶原基因的表达。 展开更多
关键词 圈套寡脱氧核苷酸(Decoy—ODN) 转录因子SP1 细胞活力 α1胶原 成纤维细胞
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知母皂苷A-Ⅲ调控ASAP1-IT1/DNMT3b/YAP1轴在非小细胞肺癌中的作用机制研究
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作者 付相君 王梅 +3 位作者 张远 李艳娜 耿彪 赵文英 《包头医学院学报》 CAS 2022年第11期10-17,33,共9页
目的:研究知母皂苷A-Ⅲ(timosaponin A-Ⅲ,TAⅢ)对非小细胞肺癌(non-small cell lung cancer,NSCLC)生长的影响及其作用机制。方法:采用不同浓度TAⅢ(5、10、15、20、25、30μmol/L)处理非小细胞肺癌细胞A549,使用CCK8法检测细胞活力。... 目的:研究知母皂苷A-Ⅲ(timosaponin A-Ⅲ,TAⅢ)对非小细胞肺癌(non-small cell lung cancer,NSCLC)生长的影响及其作用机制。方法:采用不同浓度TAⅢ(5、10、15、20、25、30μmol/L)处理非小细胞肺癌细胞A549,使用CCK8法检测细胞活力。以定量逆转录聚合酶链式反应(qRT-PCR)检测二磷酸腺苷核糖化因子鸟苷酸激酶1-内含子转录因子1(adenosine diphosphate ribosylation factor guanylate kinase 1-intronic transcript 1,ASAP1-IT1)、Yes相关蛋白1(Yes-associated protein 1,YAP1)在组织及细胞中的表达。以EDU、流式细胞术和Western blot检测ASAP1-IT1、DNA(胞嘧啶-5-)-甲基转移酶3β(DNA(cytosine-5-)-methyltransferase 3 beta,DNMT3b)、YAP1对细胞增殖情况、细胞凋亡率及其相关基因(Bax和caspase-3)与抗凋亡基因Bcl2的影响。亚硫酸氢盐测序聚合酶链式反应(Bisulfite sequencing PCR,BSP)分析检测ASAP1-IT1与YAP1的关系。RNA免疫沉淀法(RNA binding protein immunoprecipitation,RIP)和qRT-PCR法检测ASAP1-IT1与DNMT3b之间的相互作用。免疫共沉淀实验(Co-immunoprecipitation,Co-IP)检测DNMT3b与YAP1之间的关系。采用qRT-PCR方法检测TAⅢ对ASAP1-IT1/DNMT3b/YAP1轴相关基因表达的影响。结果:ASAP1-IT1和YAP1在NSCLC组织和A549细胞中表达上调,而DNMT3b表达下调,加入TAⅢ可逆转这些效应。沉默ASAP1-IT1和YAP1、过表达DNMT3b或应用TAⅢ可增加A549细胞凋亡率和细胞凋亡相关指数。TAⅢ有逆转沉默或过表达ASAP1-IT1、DNMT3b和YAP1的作用。最后发现ASAP1-IT1与DNMT3b相互作用,而DNMT3b与YAP1相互作用。结论:ASAP1-IT1/DNMT3b/YAP1轴通过调节细胞增殖和凋亡促进NSCLC进展。TAⅢ通过调节ASAP1-IT1/DNMT3b/YAP1轴抑制肺癌细胞增殖,促进其凋亡。 展开更多
关键词 二磷酸腺苷核糖化因子鸟苷酸激酶1-内含子转录因子1 Yes相关蛋白1 非小细胞肺癌 知母皂苷A-
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Interactions between GATA transcription factors and the DNasel hypersensitive sites in the human p-globin gene LCR
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作者 ZHANG Shubing, ZHAO Hui, JIANG Shu & QIAN RuolanShanghai Institute of Cell Biology, Chinese Academy of Sciences, Shanghai 200031, China Correspondence should be addressed to Qian Ruolan 《Chinese Science Bulletin》 SCIE EI CAS 2000年第21期1969-1973,共5页
In this study, we analyze the binding of nuclear proteins isolated from the hydroxyurea (Hu)-induced and uninduced HEL cells to the DNasel hypersensitive sites Ⅲ (HS3 -14991 --14716 bp) and Ⅳ(HS4 -18586-18306 bp) in... In this study, we analyze the binding of nuclear proteins isolated from the hydroxyurea (Hu)-induced and uninduced HEL cells to the DNasel hypersensitive sites Ⅲ (HS3 -14991 --14716 bp) and Ⅳ(HS4 -18586-18306 bp) in the human p-globin gene locus control region (LCR). Using Western blot assay, we demonstrate that GATA-1 transcription factor in HEL cells is increased following the induction of Hu, while GATA-2 transcription factor is decreased. Based on both the competition EMSA and the Western blot assay, our data reveal that the nuclear protein isolated from the uninduced HEL cells, which can bind to the HS3 and HS4 core DNA sequences, is mainly GATA-2; however, the nuclear proteins isolated from the Hu-induced HEL cells, which can bind to the HS3 and HS4 core DNA sequences, are mainly GATA-1 and GATA-X (a kind of unknown GATA factor). These results suggest that the erythroid specific transcription factors (GATA-1 and GATA-2) in the Hu-induced and uninduced HEL cells can selectively bind to the HS3 展开更多
关键词 DNasel HYPERSENSITIVE SITES and β-glohin gene GATA transcription factors.
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HD-Zip Ⅲ转录因子家族与植物细胞分化 被引量:13
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作者 朱莹莹 于亮亮 +1 位作者 汪杏芬 李来庚 《植物学报》 CAS CSCD 北大核心 2013年第2期199-209,共11页
细胞分化是生物生长发育的重要过程,受到一系列信号的精确调控。植物特有的转录因子HD-Zip Ⅲ在细胞分化中发挥了重要作用。该文对HD-Zip Ⅲ基因类型和结构特点进行了简要介绍,重点论述了HD-Zip Ⅲ在胚胎形态发生、顶端分生组织形成、... 细胞分化是生物生长发育的重要过程,受到一系列信号的精确调控。植物特有的转录因子HD-Zip Ⅲ在细胞分化中发挥了重要作用。该文对HD-Zip Ⅲ基因类型和结构特点进行了简要介绍,重点论述了HD-Zip Ⅲ在胚胎形态发生、顶端分生组织形成、叶极性建立和维管组织分化等发育过程中的作用,系统总结了HD-Zip Ⅲ基因在不同层次受到的调控,探讨了该家族基因与陆生维管植物进化的关系。 展开更多
关键词 细胞分化 hd-zip 植物发育 转录因子
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Identification and functional characterization of the MdHB-1 gene promoter sequence from Malus×domestica 被引量:1
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作者 WANG Hao-jie JIANG Yong-hua +6 位作者 QI Ying-wei DAI Jie-yu LIU Yan-li ZHU Xian-bo LIU Cui-hua Lü Yan-rong REN Xiao-lin 《Journal of Integrative Agriculture》 SCIE CAS CSCD 2017年第8期1730-1741,共12页
Homeobox 1 in Malusxdomestica (MdHB-1) is a transcription factor that belongs to homeodomain-leucine zipper I (HD-Zip I) protein subfamily. According to previous reports, MdHB-1 could regulate ethylene synthesis b... Homeobox 1 in Malusxdomestica (MdHB-1) is a transcription factor that belongs to homeodomain-leucine zipper I (HD-Zip I) protein subfamily. According to previous reports, MdHB-1 could regulate ethylene synthesis by binding with the MdAC01 promoter, but other functions of MdHB-1 are still unknown. To reveal more clues concerning the characters of the MdHB-1 gene promoter and the functions of MdHB-1, the promoter region of MdHB-1 was cloned from the Royal Gala apple genome and recombined with the 13-glucuronidase (GUS) gene in this study. This research was conducted in Nicotiana tabacum and supported by Agrobacterium-mediated transient transformation and bioinformatics analysis. Deletion analysis of the MdHB-1 promoter showed that the GUS gene could be activated by serially deleted promoters, and the activity promoted by 680 nucleotides (nt) was the lowest. The region, which is 266 nt upstream of the initiation code (ATG), was effective for GUS expression. Meanwhile, the activity of the MdHB-1 promoter (-1 057 nt), which was stronger than MdHB-1 promoter (-1 057 to -266 nt) and lack the 5"-untranslated region (5"-UTR), showed that 5"-UTR may have a positive effect on gene transcription. After the sequence analysis, the cis-acting elements that respond to hormones and environmental stresses were identified in the promoter region. The MdHB-1 promoter (1 057 nt) activity in Nicotiana tabacum was positively induced by ethrel and darkness, and it was suppressed by gibberellic acid (GA), whereas abscisic acid (ABA), salicylic acid (SA), wounding, and Pseudomonas syringae pv. tomato (DC3000) treatments revealed a slight auxo-action. These results reveal that the MdHB-1 promoter receive internal or external signals, and MdHB-1 may refer to many biological activities in apple, such as its stress response, development, and ripening. 展开更多
关键词 transcription factor hd-zip MdHB-1 promoter HORMONE stress
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Zinc finger structure-function in Ikaros 被引量:2
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作者 Marvin A Payne 《World Journal of Biological Chemistry》 CAS 2011年第6期161-166,共6页
The zinc finger motif was used as a vehicle for the initial discovery of Ikaros in the context of T-cell differentiation and has been central to all subsequent analyses of Ikaros function.The Ikaros gene is alternatel... The zinc finger motif was used as a vehicle for the initial discovery of Ikaros in the context of T-cell differentiation and has been central to all subsequent analyses of Ikaros function.The Ikaros gene is alternately spliced to produce several isoforms that confer diversity of function and consequently have complicated analysis of the function of Ikaros in vivo.Key features of Ikaros in vivo function are associated with six C2H2 zinc fingers;four of which are alternately incorporated in the production of the various Ikaros isoforms.Although no complete structures are available for the Ikaros protein or any of its family members,considerable evidence has accumulated about the structure of zinc fingers and the role that this structure plays in the functions of the Ikaros family of proteins.This review summarizes the structural aspects of Ikaros zinc fingers,individually,and in tandem to provide a structural context for Ikaros function and to provide a structural basis to inform the design of future experiments with Ikaros and its family members. 展开更多
关键词 IKAROS Zinc FINGER DNA binding protein transcription factor A C2H2 TANDEM
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水稻中两个同源异型结构域转录因子的亚细胞定位
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作者 李政龙 申奥 栾维江 《天津师范大学学报(自然科学版)》 CAS 2014年第3期62-65,共4页
为了对水稻同源异型结构域转录因子HD-ZipⅢ家族中的HDZ1和HDZ2进行亚细胞定位,利用RT-PCR技术从水稻cDNA中扩增HDZ1和HDZ2的编码区(去除终止密码子序列),与绿色荧光蛋白GFP编码框融合,构建2个转录因子的瞬时表达载体,采用农杆菌介导的... 为了对水稻同源异型结构域转录因子HD-ZipⅢ家族中的HDZ1和HDZ2进行亚细胞定位,利用RT-PCR技术从水稻cDNA中扩增HDZ1和HDZ2的编码区(去除终止密码子序列),与绿色荧光蛋白GFP编码框融合,构建2个转录因子的瞬时表达载体,采用农杆菌介导的转化方法转化至烟草中进行瞬时表达分析.结果表明:PCR扩增所得为目的基因片段HDZ1和HDZ2;二者与载体质粒pCAMBIA35S-GFP连接获得的融合表达载体成功移至烟草中并表达;确定HDZ1主要定位于烟草叶片的气孔中,而HDZ2定位于烟草表皮细胞的细胞膜上.二者在亚细胞中的定位不同,可能在水稻生长发育中所起的作用也不相同. 展开更多
关键词 水稻 同源异型结构域hd-zip 转录因子 绿色荧光蛋白 亚细胞定位
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Homeobox leucine zipper proteins and cotton improvement
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作者 Muzna Zahur Muhammad Ahsan Asif +3 位作者 Nadia Zeeshan Sajid Mehmood Muhammad Faheem Malik Abdul R. Asif 《Advances in Bioscience and Biotechnology》 2013年第10期15-20,共6页
Transcription factors play key roles in plant development and stress responses through their interaction with cis-elements and/or other transcription factors. Homeodomain associated leucine zipper proteins (HD-Zip) co... Transcription factors play key roles in plant development and stress responses through their interaction with cis-elements and/or other transcription factors. Homeodomain associated leucine zipper proteins (HD-Zip) constitute a family of transcription factors that are characterized by the presence of a DNA-binding domain closely linked with leucine zipper motif functioning in dimer formation. This type of association is unique to plants and considered as an excellent candidate to activate developmental responses to altering environmental conditions. Cotton is the most important fiber plant with a lot of local and commercial uses in the world. HD-Zip proteins not only have key roles in different stages of vascular and inter-fascicular fiber differentiation of cotton but also are suggested to have an important role against abiotic stress that is one of the key factors limiting cotton productivity. Plants have developed various strategies to manage stress conditions through a combination of metabolic, physiological and morphological adaptations. These adaptive changes rely largely on alterations in gene expression. Therefore, transcriptional regulators play a crucial role in stress tolerance. Being a transcription factor HD-Zip might be a useful target for genetic engineering to generate multiple stress tolerance in susceptible plants. In the following chapter, we discussed how the HD-Zip proteins would play a useful role for cotton development both in fiber production and stress adaptation. 展开更多
关键词 COTTON Stress transcription factor hd-zip Proteins HOMEOBOX LEUCINE ZIPPER
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PuHox52 promotes coordinated uptake of nitrate,phosphate, and iron under nitrogen deficiency in Populus ussuriensis 被引量:1
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作者 Ming Wei Mengqiu Zhang +9 位作者 Jiali Sun Ying Zhao Solme Pak Miaomiao Ma Yingxi Chen Han Lu Jingli Yang Hairong Wei Yuhua Li Chenghao Li 《Journal of Integrative Plant Biology》 SCIE CAS CSCD 2023年第3期791-809,共19页
It is of great importance to better understand how trees regulate nitrogen(N) uptake under N deficiency conditions which severely challenge afforestation practices, yet the underlying molecular mechanisms have not bee... It is of great importance to better understand how trees regulate nitrogen(N) uptake under N deficiency conditions which severely challenge afforestation practices, yet the underlying molecular mechanisms have not been well elucidated. Here,we functionally characterized PuHox52, a Populus ussuriensis HD-ZIP transcription factor, whose overexpression greatly enhanced nutrient uptake and plant growth under N deficiency. We first conducted an RNA sequencing experiment to obtain root transcriptome using PuHox52-overexpression lines of P. ussuriensis under low N treatment. We then performed multiple genetic and phenotypic analyses to identify key target genes of PuHox52 and validated how they acted against N deficiency under PuHox52 regulation.PuHox52 was specifically induced in roots by N deficiency, and overexpression of PuHox52promoted N uptake, plant growth, and root development. We demonstrated that several nitrate-responsive genes(PuNRT1.1, PuNRT2.4,PuCLC-b, PuNIA2, PuNIR1, and PuNLP1),phosphate-responsive genes(PuPHL1A and PuPHL1B), and an iron transporter gene(PuIRT1) were substantiated to be direct targets of PuHox52. Among them, PuNRT1.1, PuPHL1A/B, and PuIRT1 were upregulated to relatively higher levels during PuHox52-mediated responses against N deficiency in PuHox52-overexpression lines compared to WT. Our study revealed a novel regulatory mechanism underlying root adaption to N deficiency where PuHox52 modulated a coordinated uptake of nitrate, phosphate, and iron through 'PuHox52-PuNRT1.1', 'PuHox52-PuPHL1A/PuPHL1B', and'PuHox52-PuIRT1' regulatory relationships in poplar roots. 展开更多
关键词 hd-zip transcription factor iron transport nitrate transport nitrogen deprivation phosphate absorption Populus ussuriensis root architecture target gene
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乳腺癌中KiSS-1与核因子-κBp50和基质金属蛋白酶9的表达之相互关系及其临床病理意义 被引量:5
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作者 伊雪 李常颖 +3 位作者 张素华 王献华 李占清 杨方 《中华病理学杂志》 CAS CSCD 北大核心 2008年第4期238-242,共5页
目的探讨KiSS-1、核因子(NF)-κBp50和基质金属蛋白酶9(MMP-9)在乳腺癌组织中的表达和相互关系及其临床病理意义。方法应用免疫组织化学EliVision法检测152例标本(乳腺癌92例,乳腺增生30例,癌旁乳腺30例)和伴有癌转移的腋窝淋巴... 目的探讨KiSS-1、核因子(NF)-κBp50和基质金属蛋白酶9(MMP-9)在乳腺癌组织中的表达和相互关系及其临床病理意义。方法应用免疫组织化学EliVision法检测152例标本(乳腺癌92例,乳腺增生30例,癌旁乳腺30例)和伴有癌转移的腋窝淋巴结54枚中KiSS-1、NF—κBp50及MMP-9蛋白表达情况。应用原位杂交方法检测50例乳腺癌组织、20例癌旁乳腺组织中KiSS-1 mRNA的表达。应用CMIAS真彩图像分析仪对免疫组织化学和原位杂交结果进行积分吸光度(IA)值测定,并计算其平均IA值。结果(1)与癌旁乳腺组织表达比较,KiSS-1基因在乳腺癌组织学分级Ⅰ~Ⅱ级中(13.59±6.24)明显高于Ⅲ级(9.53±4.57)、TNM分期高(Ⅰ~Ⅱ期12.35±6.15,Ⅲ~Ⅳ期7.53±4.93)、在淋巴结转移率高的乳腺癌中的表达减弱(9.61±5.25,无转移组为13.06±5.89)甚至缺失;其在淋巴结转移灶(3.47±1.59)中的表达(IA值)明显低于其相应的原发灶(10.02±3.80)。乳腺癌组织中KiSS-1mRNA表达(10.84±4.90)与KiSS-1蛋白表达(11.67±6.22)有较好的一致性。(2)NF-κBp50、MMP-9在乳腺癌组织中表达上调,其上调程度随着乳腺癌分化程度的降低、TNM分期的增加、淋巴结转移及瘤块增大而逐渐增高。结论KiSS-1蛋白在乳腺癌分化程度低、淋巴结转移组中的表达下降,并分别与NF—κBp50、MMP-9蛋白表达呈负相关;NF-κBp50与MMP-9蛋白在乳腺癌中表达呈正相关,KiSS-1蛋白可能参与了乳腺癌的转移扩散。 展开更多
关键词 乳腺肿瘤 基因 KISS-1 NF—κB 明胶酶B 肿瘤转移 转录因子TF
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非小细胞肺癌中Brf1表达与预后的相关性
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作者 吕昊 易云峰 +4 位作者 宋志明 陈检明 焦昌结 陈松林 钟叔平 《中华胸心血管外科杂志》 CSCD 北大核心 2019年第8期489-493,共5页
目的研究转录因子ⅡB相关因子1(TFⅡB-related factor 1,Brf1)的表达与非小细胞肺癌(non-small cell lung cancer,NSCLC)预后的关系。方法收集2013年1月至2015年8月我院收治的96例NSCLC患者手术标本和病例资料。首先通过Western blot和R... 目的研究转录因子ⅡB相关因子1(TFⅡB-related factor 1,Brf1)的表达与非小细胞肺癌(non-small cell lung cancer,NSCLC)预后的关系。方法收集2013年1月至2015年8月我院收治的96例NSCLC患者手术标本和病例资料。首先通过Western blot和RT-qPCR比较Brf1在NSCLC组织和癌旁肺组织中的表达情况。应用免疫组化法检测Brf1在NSCLC组织中的表达,分析Brf1表达水平与临床病例特征的关系。采用Kaplan-Meier法绘制生存曲线,进行Log-rank检验单因素分析和Cox回归模型多因素分析。结果Western blot及RT-qPCR结果显示Brf1在NSCLC组织中的表达明显高于癌旁肺组织(P<0.01)。96例NSCLC组织中Brf1阳性表达率为72.9%。Brf1表达强度在低分化组中强于中-高分化组(秩均值62.33>43.89,Z=-2.914,P=0.004),有淋巴结转移组强于无转移组(秩均值60.34>42.58,Z=-3.055,P=0.002),与患者性别、年龄、吸烟情况、肿瘤大小、TNM分期和病理类型无关(P>0.05)。通过Log-rank检验进行单因素生存分析,Brf1阳性表达组生存率较阴性组低(χ^2=7.560,P<0.01)。Cox回归模型多因素分析发现,Brf1阳性表达(HR=2.043,95%CI:1.082~3.860)是影响NSCLC患者预后的一个独立观察指标。结论Brf1在NSCLC组织中存在过表达,且Brf1阴性表达者具有较好的临床预后,提示Brf1可能成为NSCLC恶性程度判定和预后评估指标之一。 展开更多
关键词 非小细胞肺癌 转录因子ⅡB相关因子1 RNA聚合酶依赖基因 预后
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