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通过新型双功能RNAi平台对作为胰腺癌治疗靶点的PDX1进行垂直整合的转化研究。

Vertically integrated translational studies of PDX1 as a therapeutic target for pancreatic cancer via a novel bifunctional RNAi platform.

作者信息

Wu J, Liu S, Yu J, Zhou G, Rao D, Jay C M, Kumar P, Sanchez R, Templeton N, Senzer N, Maples P, Nemunaitis J, Brunicardi F C

机构信息

Department of Surgery, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.

Gradalis, Carrollton, TX, USA.

出版信息

Cancer Gene Ther. 2014 Feb;21(2):48-53. doi: 10.1038/cgt.2013.84. Epub 2014 Jan 24.

Abstract

RNA interference (RNAi) represents a powerful, new tool for scientific investigation as well as a promising new form of targeted gene therapy, with applications currently in clinical trials. Bifunctional short hairpin RNA (shRNA) are synthetic RNAi molecules, engineered to utilize multiple endogenous RNAi pathways to specifically silence target genes. Pancreatic and duodenal homeobox 1 (PDX1) is a key regulator of pancreatic development, β-cell differentiation, normal β-cell function and pancreatic cancer. Our aim is to review the process of identifying PDX1 as a specific, potential RNAi target in pancreatic cancer, as well as the underlying mechanisms and various forms of RNAi, with subsequent testing and development of PDX1-targeted bifunctional shRNA therapy.

摘要

RNA干扰(RNAi)是一种强大的科学研究新工具,也是一种很有前景的新型靶向基因治疗方式,目前正在临床试验中应用。双功能短发夹RNA(shRNA)是合成的RNAi分子,经过设计可利用多种内源性RNAi途径特异性沉默靶基因。胰腺十二指肠同源盒1(PDX1)是胰腺发育、β细胞分化、正常β细胞功能和胰腺癌的关键调节因子。我们的目的是综述将PDX1鉴定为胰腺癌中特定潜在RNAi靶点的过程,以及其潜在机制和各种形式的RNAi,随后对靶向PDX1的双功能shRNA疗法进行测试和开发。

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