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黑色素瘤细胞中致癌代谢型谷氨酸受体1的激活通过蛋白激酶Cε激活细胞外信号调节激酶1/2。

Stimulation of oncogenic metabotropic glutamate receptor 1 in melanoma cells activates ERK1/2 via PKCepsilon.

作者信息

Marín Yarí E, Namkoong Jin, Cohen-Solal Karine, Shin Seung-Shick, Martino Jeffrey J, Oka Masahiro, Chen Suzie

机构信息

Susan Lehman Cullman Laboratory for Cancer Research, Department of Chemical Biology, Ernest Mario School of Pharmacy, Rutgers University, 164 Frelinghuysen Rd., Piscataway, NJ 08854, USA.

出版信息

Cell Signal. 2006 Aug;18(8):1279-86. doi: 10.1016/j.cellsig.2005.10.012. Epub 2005 Nov 21.

Abstract

Metabotropic glutamate receptor 1 (Grm1, formerly mGluR1) is a G protein coupled receptor (GPCR) normally expressed and functional in the central nervous system. Studies of our transgenic mouse melanoma model (TG-3) revealed that ectopic expression of Grm1 in melanocytes is sufficient to induce melanoma development in vivo [P.M. Pollock, K. Cohen-Solal, R. Sood, J. Namkoong, J.J. Martino, A. Koganti, H. Zhu, C. Robbins, I. Makalowska, S.S. Shin, Y. Marin, K.G. Roberts, L.M. Yudt, A. Chen, J. Cheng, A. Incao, H.W. Pinkett, C.L. Graham, K. Dunn, S.M. Crespo-Carbone, K.R. Mackason, K.B. Ryan, D. Sinsimer, J. Goydos, K.R. Reuhl, M. Eckhaus, P.S. Meltzer, W.J. Pavan, J.M. Trent, S. Chen, Nat. Genet. 34 (2003) 108-112.]. We have established and characterized several cell lines in vitro from independent mouse melanoma tumors [Y.E. Marín, J. Namkoong, S.S. Shin, J. Raines, K. Degenhardt, E. White, S. Chen, Neuropharmacol. 49 (2005) 70-79.]. These cell lines are useful tools in the studies of signaling events that may be mediated by Grm1 in transformed melanocytes. Here we show that stimulation of Grm1 by l-quisqualate, a group I metabotropic glutamate receptor agonist, results in inositol triphosphate (IP3) accumulation, and the activation of ERK1/2 in these cell lines. IP3 accumulation and ERK1/2 activation were inhibited by pretreatment of the tumor cells with a Grm1-specific antagonist (LY367385) or by dominant negative mutants of Grm1, demonstrating the specificity of these events. We also show that ERK1/2 activation by Grm1 was PKC-dependent, but cAMP and PKA-independent. PKCepsilon was shown to play a pivotal role in Grm1-mediated ERK1/2 phosphorylation. Insights into the signaling cascades mediated by Grm1 in melanoma cells may aid in the identification of key molecular targets for the future design of combined therapies for melanoma.

摘要

代谢型谷氨酸受体1(Grm1,原称mGluR1)是一种G蛋白偶联受体(GPCR),通常在中枢神经系统中表达并发挥功能。我们对转基因小鼠黑色素瘤模型(TG-3)的研究表明,黑色素细胞中Grm1的异位表达足以在体内诱导黑色素瘤的发生[P.M. Pollock,K. Cohen-Solal,R. Sood,J. Namkoong,J.J. Martino,A. Koganti,H. Zhu,C. Robbins,I. Makalowska,S.S. Shin,Y. Marin,K.G. Roberts,L.M. Yudt,A. Chen,J. Cheng,A. Incao,H.W. Pinkett,C.L. Graham,K. Dunn,S.M. Crespo-Carbone,K.R. Mackason,K.B. Ryan,D. Sinsimer,J. Goydos,K.R. Reuhl,M. Eckhaus,P.S. Meltzer,W.J. Pavan,J.M. Trent,S. Chen,《自然遗传学》34(2003)108 - 112]。我们已经从独立的小鼠黑色素瘤肿瘤中建立并鉴定了几种体外细胞系[Y.E. Marín,J. Namkoong,S.S. Shin,J. Raines,K. Degenhardt,E. White,S. Chen,《神经药理学》49(2005)70 - 79]。这些细胞系是研究Grm1在转化的黑色素细胞中可能介导的信号事件的有用工具。在此我们表明,I组代谢型谷氨酸受体激动剂L - 喹啉酸对Grm1的刺激导致这些细胞系中肌醇三磷酸(IP3)积累以及ERK1/2的激活。用Grm1特异性拮抗剂(LY367385)预处理肿瘤细胞或用Grm1的显性负性突变体可抑制IP3积累和ERK1/2激活,证明了这些事件的特异性。我们还表明,Grm1介导的ERK1/2激活是PKC依赖性的,但不依赖于cAMP和PKA。PKCε在Grm1介导的ERK1/2磷酸化中起关键作用。深入了解Grm1在黑色素瘤细胞中介导的信号级联反应可能有助于确定未来黑色素瘤联合治疗设计的关键分子靶点。

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