Raksha A Ganesh, Krishnan Venkataraman, Ravi Sirdeshmukh
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引用次数: 0
摘要
G蛋白偶联受体56 (GPR56/ADGRG1)是一种多功能粘附GPCR,参与从发育到癌症的多种生物过程。在我们早期的研究中,我们报道了GPR56在胶质母细胞瘤(GBM)中异质表达,并参与间质转化,使其成为一个有希望的治疗靶点(Ganesh et al., 2022)。尽管它在癌症中起着重要的作用,但其作用机制或信号传导尚不完全清楚。因此,基于上述研究中GPR56敲低U373-GBM细胞的转录组学、蛋白质组学和磷酸化蛋白质组学差异表达数据,以及对可能与GPR56活性相关的分子事件的详细文献挖掘,我们构建了一个可能适用于GBM间质转化的GPR56信号通路图。该图谱包含超过100个分子实体,包括激酶、受体、离子通道和其他与Wnt、整合素、钙信号、生长因子和炎症信号通路相关的分子实体。我们还考虑了可能影响通路实体活性的细胞内和细胞外因素。在这里,我们提出了GBM背景下GPR56的精心策划的信号传导图,并讨论了GPR56功能在不同轴上的相关性和可信的交叉连通性。GPR56信号传导与间质转化。
GPR56 signaling pathway network and its dynamics in the mesenchymal transition of glioblastoma.
G protein-coupled receptor 56 (GPR56/ADGRG1) is a multifunctional adhesion GPCR involved in diverse biological processes ranging from development to cancer. In our earlier study, we reported that GPR56 is expressed heterogeneously in glioblastoma (GBM) and is involved in the mesenchymal transition, making it a promising therapeutic target (Ganesh et al., 2022). Despite its important role in cancer, its mechanism of action or signaling is not completely understood. Thus, based on transcriptomic, proteomic, and phosphoproteomic differential expression data of GPR56 knockdown U373-GBM cells included in our above study along with detailed literature mining of the molecular events plausibly associated with GPR56 activity, we have constructed a signaling pathway map of GPR56 as may be applicable in mesenchymal transition in GBM. The map incorporates more than 100 molecular entities including kinases, receptors, ion channels, and others associated with Wnt, integrin, calcium signaling, growth factors, and inflammation signaling pathways. We also considered intracellular and extracellular factors that may influence the activity of the pathway entities. Here we present a curated signaling map of GPR56 in the context of GBM and discuss the relevance and plausible cross-connectivity across different axes attributable to GPR56 function. GPR56 signaling and mesenchymal transition.
期刊介绍:
The Journal of Cell Communication and Signaling provides a forum for fundamental and translational research. In particular, it publishes papers discussing intercellular and intracellular signaling pathways that are particularly important to understand how cells interact with each other and with the surrounding environment, and how cellular behavior contributes to pathological states. JCCS encourages the submission of research manuscripts, timely reviews and short commentaries discussing recent publications, key developments and controversies.
Research manuscripts can be published under two different sections :
In the Pathology and Translational Research Section (Section Editor Andrew Leask) , manuscripts report original research dealing with celllular aspects of normal and pathological signaling and communication, with a particular interest in translational research.
In the Molecular Signaling Section (Section Editor Satoshi Kubota) manuscripts report original signaling research performed at molecular levels with a particular interest in the functions of intracellular and membrane components involved in cell signaling.