Carlson Coby B, Mashock Michael J, Bi Kun
Invitrogen Discovery Assays and Services, Cell Systems Division, Invitrogen (Part of Life Technologies), Madison, Wisconsin 53719, USA.
J Biomol Screen. 2010 Mar;15(3):327-34. doi: 10.1177/1087057109357788. Epub 2010 Feb 9.
The authors recently reported the development and application of multiple LanthaScreen cellular assays to interrogate specific steps within the PI3K/Akt pathway. The importance of this signaling cascade in regulating fundamental aspects of cell growth and survival, as well as in the progression of cancer, underscores the need for portable cell-based assays for compound profiling in multiple disease-relevant cell backgrounds. To meet this need, the authors have now expanded their LanthaScreen assay platform across a variety of cell types using a gene delivery technology known as BacMam. Here, they have demonstrated the successful detection of Akt-dependent phosphorylation of PRAS40 at Thr246 in 10 different cell lines harboring mutations known to activate the PI3K/Akt pathway. In addition, they generated inhibitory profiles of 17 known pathway inhibitors in these same cells to validate the approach of using the BacMam-enabled LanthaScreen cellular assay format to rapidly profile compounds in disease-relevant cell types. Importantly, their results provide a broad illustration of how the genetic alterations that affect PI3K/Akt signaling can also influence the inhibitory profile of a given compound.
作者最近报道了多种LanthaScreen细胞分析方法的开发与应用,用于探究PI3K/Akt信号通路中的特定步骤。这一信号级联在调节细胞生长和存活的基本方面以及癌症进展中的重要性,凸显了在多种与疾病相关的细胞背景下进行基于细胞的化合物分析的便携式检测方法的必要性。为满足这一需求,作者现在使用一种名为BacMam的基因传递技术,将他们的LanthaScreen分析平台扩展到了多种细胞类型。在此,他们展示了在10种携带已知可激活PI3K/Akt信号通路突变的不同细胞系中,成功检测到PRAS40在Thr246位点的Akt依赖性磷酸化。此外,他们还在这些相同的细胞中生成了17种已知信号通路抑制剂的抑制谱,以验证使用基于BacMam的LanthaScreen细胞分析形式在与疾病相关的细胞类型中快速分析化合物的方法。重要的是,他们的结果广泛说明了影响PI3K/Akt信号传导的基因改变如何也能影响给定化合物的抑制谱。