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101.
Loss of TAB3 expression by shRNA exhibits suppressive bioactivity and increased chemical sensitivity of ovarian cancer cell lines via the NF‐κB pathway 下载免费PDF全文
Chengwei Duan Jie Chen Ming Su Yunfeng Jin Yan Deng Di Wang Caiwen Chen Linsen Zhou Jialin Cheng Wei Wang Qinghua Xi 《Cell proliferation》2016,49(6):657-668
Ovarian cancer is a leading cause of death among gynaecologic malignancies. Despite many years of research, it still remains sparing in reliable diagnostic markers and methods for early detection and screening. Transforming growth factor β‐activated protein kinase 1 (TAK1)‐binding protein 3 (TAB3) was initially characterized as an adapter protein essential for TAK1 activation in response to IL‐1β or TNFα, however, the physiological role of TAB3 in ovarian cancer tumorigenesis is still not fully understood. In this study, we evaluated the effects of TAB3 on ovarian cancer cell lines. Expressions of TAB3 and PCNA (proliferating cell nuclear antigen) were found to be gradually increased in EOC tissues and cell lines, by western blot analysis and qRT‐PCR. Distribution of TAB3 was further analysed by immunohistochemistry. In vitro, knockdown of TAB3 expression in HO8910 or SKOV3 ovarian cancer cells significantly inhibited bioactivity of ovarian cancer cells, including proliferation and cell‐cycle distribution, and promoted chemical sensitivity to cisplatin and paclitaxel treatment via inhibiting NF‐κB pathways. In conclusion, our study strongly suggests a novel function of TAB3 as an oncogene that could be used as a biomarker for ovarian cancer. It provides a new insight into the potential mechanism for therapeutic targeting, in chemotherapy resistance, common in ovarian cancer. 相似文献
102.
不同小麦品种对播娘蒿的影响 总被引:2,自引:0,他引:2
播娘蒿是黄淮麦区主要田间杂草,在管理粗放的麦田,播娘蒿密度可达100株·m-2以上,严重影响了小麦的产量和品质。因此,对小麦-杂草复合体中杂草的生长发育规律进行研究,寻找降低草害的有效途径引起许多学者极大关注[1,2],而目前有关防除麦田杂草的研究多集中于化学防治方面[3]。然而,出于环境保护和经济成本上的考虑,化学除草受到了挑战。研究人员[4,5]发现,不同物种在竞争力上存在差异,禾谷类作物属于竞争力很强的作物[6],冬小麦及冬黑麦又是其中竞争力最强的物种。就小麦栽培种而言,存在着不同的品种类型,研究不同小麦品种对杂草的抑制作… 相似文献
103.
Jashanpreet Kaur Shu Yao Duan Lea A. I. Vaas Anahit Penesyan Wieland Meyer Ian T. Paulsen Helena Nevalainen 《PloS one》2015,10(3)
Genotyping studies of Australian Scedosporium isolates have revealed the strong prevalence of a recently described species: Scedosporium aurantiacum. In addition to occurring in the environment, this fungus is also known to colonise the respiratory tracts of cystic fibrosis (CF) patients. A high throughput Phenotype Microarray (PM) analysis using 94 assorted substrates (sugars, amino acids, hexose-acids and carboxylic acids) was carried out for four isolates exhibiting different levels of virulence, determined using a Galleria mellonella infection model. A significant difference was observed in the substrate utilisation patterns of strains displaying differential virulence. For example, certain sugars such as sucrose (saccharose) were utilised only by low virulence strains whereas some sugar derivatives such as D-turanose promoted respiration only in the more virulent strains. Strains with a higher level of virulence also displayed flexibility and metabolic adaptability at two different temperature conditions tested (28 and 37°C). Phenotype microarray data were integrated with the whole-genome sequence data of S. aurantiacum to reconstruct a pathway map for the metabolism of selected substrates to further elucidate differences between the strains. 相似文献
104.
目的探讨炎症细胞因子白介素-1β(interleukin-1βIL-1β)对高糖刺激的人肾小管上皮细胞转分化的影响。-方法体外培养人肾近曲小管上皮细胞株(HKCs),随机分为正常对照组(5.5 mmol/L normal glucose);高糖组(30 mmol/L high glucose);高糖+IL-1β(5ng/ml)组。分别于处理后24h、48h、72h收集细胞,采用免疫细胞化学染色和Western蛋白印迹法检测细胞角蛋白-18(cytokeratin-18 CK-18)、α-平滑肌肌动蛋白(α-smooth muscle actinα-SMA)水平。结果高糖能够诱导肾小管上皮细胞α-SMA蛋白的合成增加,而肾小管上皮细胞的标志物CK-18的表达逐渐减少;IL-1β与高糖同时刺激可使肾小管上皮细胞α-SMA蛋白表达进一步增多,而其自身标志物CK-18的表达则明显下降。结论炎症因子IL-1β能增强高糖对肾小管上皮细胞转分化的作用。 相似文献
105.
Spermatogenesis in the blue swimming crab, Portunus pelagicus, is described by light and electron microscopy. The testis is composed of anterior (AT) and posterior (PT) lobes, that are partitioned into lobules by connective tissue trabecula, and further divided into zones (germinal, transformation and evacuation), each with various stages of cellular differentiation. The vas deferens is classified into three distinct regions: anterior (AVD), median (MVD), and posterior (PVD), on the presence of spermatophores and two secretions, termed substance I and II. Based on the degree and patterns of heterochromatin, spermatogenesis is classified into 13 stages: two spermatogonia (SgA and SgB), six primary spermatocytes (leptotene, zygotene, pachytene, diplotene, diakinesis, and metaphase), a secondary spermatocyte (SSc), three spermatids (St 1-3), and a mature spermatozoon. Spermatid stages are differentiated by chromatin decondensation and the formation of an acrosomal complex, which is unique to brachyurans. Mature spermatozoa are aflagellated, and have a nuclear projection and a spherical acrosome. AUT-PAGE and Western blots show that, during chromatin decondensation, there is a reduction of most histones, with only small amounts of H2B and H3 remaining in mature spermatozoa. 相似文献
106.
Binggang Ma Xiaoyu Duan Chao Ma Jianxin Niu Huping Zhang Lizhong Pan 《Plant Molecular Biology Reporter》2008,26(3):199-212
The presence of antibiotic-resistant genes in genetically engineered crops together with the target gene has generated a number
of environmental and consumer concerns. In order to alleviate public concerns over the safety of food derived from transgenic
crops, marker gene elimination is desirable. Marker-free transgenic tomato plants were obtained by using a salicylic-acid-regulated
Cre–loxP-mediated site-specific DNA recombination system in which the selectable marker neomycin phosphotransferase nptII and cre genes were flanked by two directly oriented loxP sites. Upon induction by salicylic acid, the cre gene produced a recombinase that eliminated sequences encoding nptII and cre genes, sandwiched by two loxP sites from the tomato genome. Regenerant plants with the Cre–loxP system were obtained by selection on kanamycin media and polymerase chain reaction (PCR) screening. Transgenic plants were
screened for excision by PCR using nptII, cre, and PR-1a promoter primers following treatment with salicylic acid. The footprint of the excision was determined by sequencing
the T-DNA borders after a perfect recombination event. The excision efficiency was 38.7%. A new plant transformation vector,
pBLNSC (Genbank accession number EU327497), was developed, containing six cloning sites and the self-excision system. This
provided an effective approach to eliminate the selectable marker gene from transgenic tomato, thus expediting public acceptance
of genetically modified tomato. 相似文献
107.
获取全长cDNA若干方法的比较 总被引:2,自引:0,他引:2
生物技术突飞猛进大大提高了人类认识自身及与人类息息相关的生命现象的能力。近几年内 ,人类 [1,2 ]、模式生物拟南芥 ( Arabidopsis thaliana) [3 5]及水稻的基因组测序 [6,7]的草图相继完成 ,给人类又提出了新的挑战 :如何鉴定这些序列的功能及如何解析生命现象的基因本质 ,这是一个更加庞大而又极富挑战性的课题 ,正促使一门新的学科即功能基因组学 ( Functional genomics)的产生与蓬勃发展。不论功能基因组学多么深奥 ,其认识基因功能的基本前提是获取可能有相关功能的基因之全长编码序列。其中 ,全长 c DNA序列的获取是正确地注释基… 相似文献
108.
109.
禽流感病毒H5N1 NS1蛋白是一种非结构蛋白,在病毒感染过程中发挥着重要的作用.构建基因截短的重组蛋白,可为进一步研究NS1不同结构域与宿主蛋白间的相互作用奠定基础.在成功克隆禽流感病毒H5N1全长NS1基因并测序的基础上,将部分截短基因序列克隆到表达栽体pET28a(+)上,构建基因截短的重组表达质粒pET28a-NS1-RBD和pET28a-NS1-ED,转化大肠埃希菌BL21(DE3),阳性重组质粒经IPTG诱导表达后进行SDS-PAGE检测,获得预期蛋白的表达,然后利用Ni-NTA树脂蛋白纯化系统对重组蛋白进行纯化,并通过Western Blotting进一步确认NS1及截短体蛋白的表达.结果表明,实验成功构建禽流感病毒H5N1亚型的NS1蛋白截短体,并在大肠埃希菌中高效表达,这为进一步研究NS1蛋白不同结构域与宿主蛋白的相互作用提供了实验材料,为深入研究NS1蛋白的生物学功能奠定了坚实基础. 相似文献
110.
Linlin Tang Huadan Ye Qingxiao Hong Lingyan Wang Qinwen Wang Hongwei Wang Leiting Xu Shizhong Bu Lina Zhang Jia Cheng Panpan Liu Yanping Le Meng Ye Yifeng Mai Shiwei Duan 《Gene》2014