Inhibitory Effects of Phenylacetic Acid on Proliferation of Human Pancreatic Carcinoma BXPC-3 Cells

来源 :高等学校化学研究(英文版) | 被引量 : 0次 | 上传用户:ss1725
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
The effect and mechanism of phenylacetic acid on the proliferation of pancreatic carcinoma cells were investigated in cultured pancreatic carcinoma BXPC-3 cells by means of 3-(4,5-dimethylthiazol-2-yl)-2,5- diphenyltetrazolium bromide assay and flow cytometry assay. The results show that the treatment of pancreatic carcinoma cells with phenylacetic acid significantly inhibited the cell proliferation in time-dependent and dose-dependent manners. The proliferation of BXPC-3 cells was inhibited at the stage of S phase, the cells at the end stage of S phase were accumulated abundantly, and thus DNA synthesis could not be accomplished entirely. In addition, the expression of adenosine deaminases acting on RNA(ADARs) mRNA in BXPC-3 cells and pancreatic carcinoma specimen were detected by RT-PCR. Having been treated with phenylacetic acid, ADAR2 mRNA in BXPC-3 cells was significantly decreased, the differences were of statistical significance(P
其他文献
本文通过对荣华二采区10
The temperature curve in the solar chromosphere has puzzled astronomers for a long time.Referring to the structure of supergranular cells,we propose an in ducti
One new dammarane-type triterpene saponin, named (20S)-3β,20,21-trihydroxydammar-24-ene 3-O[α-L- rhamnopyranosyl-(1→2)][β-D-xylopyranosyl(l→3)]-β-D-glucop
The thermodynamic properties of the reaction of amide and formaldehyde were calculated via B3LYP method when substituents chosen included CH3, CH2CH3, CH2CH2CH3
This paper describes an experimental investigation on the flow characteristics within a rotating cylinder containing a rolling bed of sand.The axis of the cylin
Multi-Relaxation-Time Lattice Boltzmann Method (MRT LBM) is of better numerical stability and has attracted more and more research interests. The previous MRT L
为探究吕家坨井田地质构造格局,根据钻孔勘探资料,采用分形理论和趋势面分析方法,研究了井田7
A series of novel azasterols 8a―8h and 10a―10c were synthesized from the key intermediate 6 by acylation and deprotection. Compound 6 was obtained through a s
[Hmim]3PW12O40 was developed and used in the acetalization of carbonyl compounds in excellent yields. The ionic liquid-heteropoly acid hybrid compound and react
本文通过对荣华二采区10