期刊文献+
共找到5篇文章
< 1 >
每页显示 20 50 100
The influence of down-regulation of ACP1 by RNAi on the metastasis capability of osteosarcoma cell line MG-63
1
作者 Bo Zhu Anmin Chen Fengjing Guo 《The Chinese-German Journal of Clinical Oncology》 CAS 2009年第8期481-484,共4页
Objective: The aim of this study was to study the inhibition effect of small interfering RNAs (siRNA) on gene expression in MG-63 cells,and to study the inhibitory effect on metastasis of MG-63. Methods: A plasmid... Objective: The aim of this study was to study the inhibition effect of small interfering RNAs (siRNA) on gene expression in MG-63 cells,and to study the inhibitory effect on metastasis of MG-63. Methods: A plasmid of a short hairpin RNA targeting acid phosphatase 1 (ACP1) was constructed and transfected into MG-63 cell line. ACP1 expression of MG-63 cells before and after transfection was detected by RT-PCR and Western blot. The capacity of adhesion, migration and inva- sion was examined by adhesion assay, migration assay and transwell assay. Results: The recombinant plasmid pGenesil-l/ ACPI-shRNA was successfully constructed, shRNA efficiently inhibited the expression of ACPI by gene and protein level and suppressed cell migration. The adhesion decreased from 96.41±8.83 to 43.38 ± 6.03 (P 〈 0.01), invasion ability from 56.5 ± 4.8 to 36.3 ± 6.1 (P 〈 0.05). Conclusion: Down-regulating ACP1 by shRNA reduced the capacity of metastasis of MG-63 cell,which providing a novo-approach to biotherapy of cancer. 展开更多
关键词 acid phosphatase 1 (acp1) small interfering RNAs (siRNA) OSTEOSARCOMA
下载PDF
Smoking, ACP<sub>1</sub>and Infertility in Subjects with Varicocele
2
作者 Anna Neri Maria Banci +2 位作者 Adalgisa Pietropolli Fulvia Gloria-Bottini Andrea Magrini 《Health》 2019年第10期1331-1337,共7页
Several studies suggest that smoking may have detrimental effect on seminal parameters and that genetic polymorphisms may influence this effect. In the present paper we have examined the relationship between ACP1 geno... Several studies suggest that smoking may have detrimental effect on seminal parameters and that genetic polymorphisms may influence this effect. In the present paper we have examined the relationship between ACP1 genotypes and the association of smoking and infertility in a sample of men with varicocele. 126 subjects with varicocele were studied. ACP1 genotype was determined by DNA analysis and statistical analyses were performed by SPSS software. In general there is a protective action of low activity *A/*B genotype against infertility that is much more marked in smokers than in non-smokers. If confirmed in other clinical settings, determinations of ACP1 genotype could have practical importance to evaluate the risk of infertility in smokers with varicocele. 展开更多
关键词 SMOKING acp1 VARICOCELE INFERTILITY Genetic Polymorphism
下载PDF
IGIACP1 predicts the prognosis in multiple myeloma patients
3
作者 Xiangyu Meng Xiaoping Liu +2 位作者 Chunrui Li Cheng Fang Li He 《Oncology and Translational Medicine》 2017年第5期217-220,共4页
Objective The aim of this study was to investigate the prognostic relevance of acid phosphatase 1(ACP1) expression in myeloma patients by using Gene Expression Omnibus(GEO) datasets.Methods A comprehensive search was ... Objective The aim of this study was to investigate the prognostic relevance of acid phosphatase 1(ACP1) expression in myeloma patients by using Gene Expression Omnibus(GEO) datasets.Methods A comprehensive search was performed in the GEO database in order to find appropriate datasets. The expression level of ACP1 was extracted from the dataset involving both newly diagnosed and relapsed myeloma patients, and a comparison was made. Clinical follow-up data and ACP1 expression were extracted, and survival analysis of overall survival was performed to compare the high-(top quartile) and low-expression(bottom quartile) groups. Analyses using Kaplan-Meier estimation, log-rank test, and restricted mean survival time(RMST) comparison were performed.Results The GSE 6477 dataset was used to make a comparison of the ACP1 expression levels among patients with newly diagnosed and relapsed myeloma. The ACP1 expression level was significantly higher in the relapsed group than in the newly diagnosed group [mean difference =-262.9, 95% confidence interval(CI) =(-420.2,-105.5), P = 0.002]. The GSE 2658 dataset was used for investigating the prognostic relevance of ACP1 expression in myeloma. The ACP1 high-expression group had a significantly worse prognosis [low vs high: hazard ratio = 0.54, 95% CI =(0.31, 0.95); χ2 = 5.02, log rank P = 0.0314]. The median survival was 55.9 months in the high-expression group and was not reached in the low-expression group. The restricted mean time loss(95% CI) was 11.03(12.97, 23.11) and 18.04(12.97, 23.11) for the low-and high-expression groups, respectively. The ratio of RMST(95% CI) between the two groups(high vs low) was 0.87(0.77, 0.99; P = 0.03).Conclusion Our study, for the first time, showed that ACP1 predicts the prognosis in multiple myeloma patients. Further studies are needed to determine the potential mechanism by which ACP1 is associated with clinical outcomes and should focus on the differential roles of low-molecular-weight protein tyrosine phosphatase(LMWPTP) isoforms. 展开更多
关键词 multiple MYELOMA PROGNOSIS acp1 LOW-MOLECULAR-WEIGHT protein TYROSINE PHOSPHATASE (LMWPTP)
下载PDF
基于质粒分子的转cry1Aa基因棉花定量PCR方法的建立
4
作者 苏长青 《福建农业学报》 CAS CSCD 北大核心 2020年第6期569-575,共7页
【目的】转cry1Aa基因棉花南农6号为我国未经批准商业化种植的棉花品种。为监测其非法种植,解决阳性标准品不容易获得的问题,构建适合转cry1Aa基因棉花南农6号品系特异性检测的质粒分子pMD-NN6,以该质粒分子作为标准物质,建立相应的实... 【目的】转cry1Aa基因棉花南农6号为我国未经批准商业化种植的棉花品种。为监测其非法种植,解决阳性标准品不容易获得的问题,构建适合转cry1Aa基因棉花南农6号品系特异性检测的质粒分子pMD-NN6,以该质粒分子作为标准物质,建立相应的实时荧光定量PCR方法。【方法】根据南农6号转化体特异序列和棉花内标准基因acp1设计引物,采用重叠PCR方法构建质粒分子;以质粒分子作为标准物质,南农6号转化体特异序列为靶标,建立了南农6号棉花特异性定量检测方法。【结果】构建的质粒全长为3148 bp,含有南农6号品系特异性序列和棉花acp1基因序列两个靶标片段的质粒分子,定量标准曲线斜率和扩增效率均符合要求,定量检测限为30拷贝。两个已知南农6号含量的混合样品(2.0%和0.5%)定量检测的准确度标准偏差均在±25%范围内,精确度相对标准差均≤25%。【结论】建立的PCR定量检测方法可以用于含有南农6号转基因棉花产品的品系特异性定量检测,所构建的标准质粒pMD-NN6可以代替其基因组DNA作为标准物质使用。 展开更多
关键词 抗虫棉 质粒分子 acp1基因 cry1Aa基因 品系特异性实时PCR
下载PDF
白念珠菌酰基载体蛋白1的制备
5
作者 孟玲宁 刘锦燕 +1 位作者 王钰婷 项明洁 《诊断学理论与实践》 2018年第6期645-649,共5页
目的 :通过在大肠埃希菌BL21中表达白念珠菌酰基载体蛋白1(acyl carrier protein 1,Acp1),以制备高纯度的目的蛋白。方法:采用PCR扩增目的基因ACP1后,在序列的C端拼接上6xHis tag及终止子,拼接完成后连接构建到质粒中,成为原核表达载体p... 目的 :通过在大肠埃希菌BL21中表达白念珠菌酰基载体蛋白1(acyl carrier protein 1,Acp1),以制备高纯度的目的蛋白。方法:采用PCR扩增目的基因ACP1后,在序列的C端拼接上6xHis tag及终止子,拼接完成后连接构建到质粒中,成为原核表达载体pET30a-ACP1,转化入大肠埃希菌感受态细胞BL21中,通过异丙基-β-D-硫代半乳糖苷(isopropyl-beta-D-thiogalactopyranoside, IPTG)诱导表达。收集表达产物后通过镍离子螯合柱纯化,最终利用考马斯亮蓝Bradford法测得目的蛋白含量。结果:白念珠菌酰基载体蛋白Acp1在大肠埃希菌BL21中高效表达;抽提纯化蛋白后行蛋白电泳检测,结果显示,在还原条件下Acp1一直存在2条相对分子质量为17 000的条带。经还原和非还原电泳及蛋白印迹法检测,结果显示该蛋白在非还原状态下有聚集。利用Bradford方法测得蛋白Acp1浓度为2.68 mg/mL。结论:成功制备了白念珠菌酰基载体蛋白Acp1,为后期利用荧光偏振法筛选靶点为Ppt2酶的临床药物提供基础。 展开更多
关键词 白念珠菌 酰基载体蛋白acp1 蛋白制备纯化
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部