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本文引用的文献

1
Identification of two novel SH3PXD2B gene mutations in Frank-Ter Haar syndrome by exome sequencing: Case report and review of the literature.通过外显子组测序鉴定弗兰克 - 特哈综合征中的两个新型SH3PXD2B基因突变:病例报告及文献综述
Gene. 2017 Sep 10;628:190-193. doi: 10.1016/j.gene.2017.07.011. Epub 2017 Jul 8.
2
ADAM12 induction by Twist1 promotes tumor invasion and metastasis via regulation of invadopodia and focal adhesions.Twist1 诱导的 ADAM12 通过调节侵袭伪足和黏着斑促进肿瘤侵袭和转移。
J Cell Sci. 2017 Jun 15;130(12):2036-2048. doi: 10.1242/jcs.198200. Epub 2017 May 3.
3
Discs large homolog 5 decreases formation and function of invadopodia in human hepatocellular carcinoma via Girdin and Tks5.Discs large 同源物 5 通过 Girdin 和 Tks5 减少人肝癌细胞侵袭伪足的形成和功能。
Int J Cancer. 2017 Jul 15;141(2):364-376. doi: 10.1002/ijc.30730. Epub 2017 May 9.
4
Stimulus-dependent dissociation between XB130 and Tks5 scaffold proteins promotes airway epithelial cell migration.XB130与Tks5支架蛋白之间的刺激依赖性解离促进气道上皮细胞迁移。
Oncotarget. 2016 Nov 22;7(47):76437-76452. doi: 10.18632/oncotarget.13261.
5
The role of Tks adaptor proteins in invadopodia formation, growth and metastasis of melanoma.Tks衔接蛋白在黑色素瘤侵袭伪足形成、生长和转移中的作用。
Oncotarget. 2016 Nov 29;7(48):78473-78486. doi: 10.18632/oncotarget.12954.
6
The role and regulation of Rab40b-Tks5 complex during invadopodia formation and cancer cell invasion.Rab40b-Tks5复合物在侵袭性伪足形成和癌细胞侵袭过程中的作用及调控
J Cell Sci. 2016 Dec 1;129(23):4341-4353. doi: 10.1242/jcs.193904. Epub 2016 Oct 27.
7
XB130/Tks5 scaffold protein interaction regulates Src-mediated cell proliferation and survival.XB130/Tks5支架蛋白相互作用调节Src介导的细胞增殖与存活。
Mol Biol Cell. 2015 Dec 1;26(24):4492-502. doi: 10.1091/mbc.E15-07-0483. Epub 2015 Oct 7.
8
The invadopodia scaffold protein Tks5 is required for the growth of human breast cancer cells in vitro and in vivo.侵袭性伪足支架蛋白Tks5是人类乳腺癌细胞在体外和体内生长所必需的。
PLoS One. 2015 Mar 31;10(3):e0121003. doi: 10.1371/journal.pone.0121003. eCollection 2015.
9
Regulation of ECM degradation and axon guidance by growth cone invadosomes.生长锥侵袭小体对细胞外基质降解和轴突导向的调控。
Development. 2015 Feb 1;142(3):486-96. doi: 10.1242/dev.108266. Epub 2015 Jan 6.
10
Multiparametric classification links tumor microenvironments with tumor cell phenotype.多参数分类将肿瘤微环境与肿瘤细胞表型联系起来。
PLoS Biol. 2014 Nov 11;12(11):e1001995. doi: 10.1371/journal.pbio.1001995. eCollection 2014 Nov.

Tks 衔接蛋白一览。

Tks adaptor proteins at a glance.

机构信息

Department of Cell, Developmental & Cancer Biology, Oregon Health and Science University, Portland, OR, USA.

Department of Cell, Developmental & Cancer Biology, Oregon Health and Science University, Portland, OR, USA

出版信息

J Cell Sci. 2018 Jan 8;131(1):jcs203661. doi: 10.1242/jcs.203661.

DOI:10.1242/jcs.203661
PMID:29311151
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5818055/
Abstract

Tyrosine kinase substrate (Tks) adaptor proteins are considered important regulators of various physiological and/or pathological processes, particularly cell migration and invasion, and cancer progression. These proteins contain PX and SH3 domains, and act as scaffolds, bringing membrane and cellular components in close proximity in structures known as invadopodia or podosomes. Tks proteins, analogous to the related proteins p47, p40 and NoxO1, also facilitate local generation of reactive oxygen species (ROS), which aid in signaling at invadopodia and/or podosomes to promote their activity. As their name suggests, Tks adaptor proteins are substrates for tyrosine kinases, especially Src. In this Cell Science at a Glance article and accompanying poster, we discuss the known structural and functional aspects of Tks adaptor proteins. As the science of Tks proteins is evolving, this article will point out where we stand and what still needs to be explored. We also underscore pathological conditions involving these proteins, providing a basis for future research to develop therapies for treatment of these diseases.

摘要

酪氨酸激酶底物(Tks)衔接蛋白被认为是各种生理和/或病理过程的重要调节剂,特别是细胞迁移和侵袭以及癌症进展。这些蛋白质含有 PX 和 SH3 结构域,作为支架,将膜和细胞成分在称为侵袭伪足或足突的结构中紧密靠近。Tks 蛋白类似于相关蛋白 p47、p40 和 NoxO1,也有助于局部产生活性氧(ROS),这有助于在侵袭伪足和/或足突处进行信号转导,以促进其活性。顾名思义,Tks 衔接蛋白是酪氨酸激酶的底物,尤其是Src。在本期《细胞科学一瞥》文章及其配套海报中,我们讨论了 Tks 衔接蛋白的已知结构和功能方面。随着 Tks 蛋白科学的发展,本文将指出我们的立场以及仍需要探索的地方。我们还强调了涉及这些蛋白质的病理状况,为未来的研究提供了基础,以开发治疗这些疾病的疗法。