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1.
Biochem Biophys Res Commun ; 462(4): 389-95, 2015 Jul 10.
Artigo em Inglês | MEDLINE | ID: mdl-25982477

RESUMO

We previously identified 14-3-3ß as a tumor-specific isoform of 14-3-3 protein in astrocytoma, but its functional role in glioma cells and underlying mechanisms are poorly understood. In the present study, we investigated the effects of 14-3-3ß inhibition in human glioma U87 cells using specific targeted small interfering RNA (siRNA). The results showed that 14-3-3ß is highly expressed in U87 cells but not in normal astrocyte SVGp12 cells. Knockdown of 14-3-3ß by Si-14-3-3ß transfection significantly decreased the cell viability but increased the LDH release in a time-dependent fashion in U87 cells, and these effects were accompanied with G0/G1 cell cycle arrest and apoptosis. In addition, 14-3-3ß knockdown induced ER stress in U87 cells, as evidenced by ER calcium release, increased expression of XBP1S mRNA and induction of ER related pro-apoptotic factors. Down-regulation of 14-3-3ß significantly decreased the nuclear localization of ß-catenin and inhibited Topflash activity, which was shown to be reversely correlated with CHOP. Furthermore, Si-CHOP and sFRP were used to inhibit CHOP and Wnt, respectively. The results showed that the anti-cancer effects of 14-3-3ß knockdown in U87 cells were mediated by increased expression of CHOP and followed inhibition of Wnt/ß-catenin pathway. In summary, the remarkable efficiency of 14-3-3ß knockdown to induce apoptotic cell death in U87 cells may find therapeutic application for the treatment of glioma patients.


Assuntos
Proteínas 14-3-3/metabolismo , Neoplasias Encefálicas/metabolismo , Regulação para Baixo , Retículo Endoplasmático/metabolismo , Glioma/metabolismo , Estresse Oxidativo , Fator de Transcrição CHOP/metabolismo , Proteínas Wnt/metabolismo , Proteínas 14-3-3/genética , Apoptose , Sequência de Bases , Neoplasias Encefálicas/patologia , Linhagem Celular Tumoral , Primers do DNA , Técnicas de Silenciamento de Genes , Glioma/patologia , Humanos , Reação em Cadeia da Polimerase em Tempo Real
2.
Electrophoresis ; 36(2): 271-6, 2015 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-25363755

RESUMO

In this study, we describe the developmental validation assay performed on a novel designed STR multiplex system, AGCU 21+1 STR kit. This kit contains a sex-determining locus amelogenin and 21 noncombined DNA index system STR loci, that are, D6S474, D12ATA63, D22S1045, D10S1248, D1S1677, D11S4463, D1S1627, D3S4529, D2S441, D6S1017, D4S2408, D19S433, D17S1301, D1GATA113, D18S853, D20S482, D14S1434, D9S1122, D2S1776, D10S1435, and D5S2500. The 21+1 kit was validated by a series of tests including optimized PCR conditions, sensitivity, precision and accuracy, stutter ratio, DNA mixture, inhibitors, and species specificity according to the revised validation guidelines issued by the Scientific Working Group on DNA Analysis Methods (SWGDAM). Our results in this study show that the kit is a useful tool for forensic application.


Assuntos
Repetições de Microssatélites , Reação em Cadeia da Polimerase Multiplex/métodos , Animais , Primers do DNA , Ciências Forenses/métodos , Humanos , Magnésio , Kit de Reagentes para Diagnóstico , Sensibilidade e Especificidade , Análise para Determinação do Sexo , Especificidade da Espécie , Taq Polimerase , Temperatura
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