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本文引用的文献

1
Genomic analysis identifies new drivers and progression pathways in skin basal cell carcinoma.基因组分析鉴定出皮肤基底细胞癌的新驱动基因和进展途径。
Nat Genet. 2016 Apr;48(4):398-406. doi: 10.1038/ng.3525. Epub 2016 Mar 7.
2
Phosphorylation-Dependent Regulation of the DNA Damage Response of Adaptor Protein KIBRA in Cancer Cells.衔接蛋白KIBRA在癌细胞中DNA损伤反应的磷酸化依赖性调控
Mol Cell Biol. 2016 Apr 15;36(9):1354-65. doi: 10.1128/MCB.01004-15. Print 2016 May.
3
Human phosphatase CDC14A is recruited to the cell leading edge to regulate cell migration and adhesion.人类磷酸酶CDC14A被招募到细胞前沿以调节细胞迁移和黏附。
Proc Natl Acad Sci U S A. 2016 Jan 26;113(4):990-5. doi: 10.1073/pnas.1515605113. Epub 2016 Jan 8.
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Kibra and aPKC regulate starvation-induced autophagy in Drosophila.Kibra和非典型蛋白激酶C调节果蝇中饥饿诱导的自噬。
Biochem Biophys Res Commun. 2015;468(1-2):1-7. doi: 10.1016/j.bbrc.2015.11.011. Epub 2015 Nov 10.
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Mutational dynamics between primary and relapse neuroblastomas.原发和复发神经母细胞瘤之间的突变动态。
Nat Genet. 2015 Aug;47(8):872-7. doi: 10.1038/ng.3349. Epub 2015 Jun 29.
6
Sox2 antagonizes the Hippo pathway to maintain stemness in cancer cells.Sox2拮抗Hippo信号通路以维持癌细胞的干性。
Nat Commun. 2015 Apr 2;6:6411. doi: 10.1038/ncomms7411.
7
MiR-21 promotes intrahepatic cholangiocarcinoma proliferation and growth in vitro and in vivo by targeting PTPN14 and PTEN.微小RNA-21通过靶向蛋白酪氨酸磷酸酶非受体型14和磷酸酶及张力蛋白同源物在体外和体内促进肝内胆管癌的增殖和生长。
Oncotarget. 2015 Mar 20;6(8):5932-46. doi: 10.18632/oncotarget.3465.
8
The tyrosine phosphatase PTPN14 (Pez) inhibits metastasis by altering protein trafficking.酪氨酸磷酸酶PTPN14(Pez)通过改变蛋白质运输来抑制转移。
Sci Signal. 2015 Feb 17;8(364):ra18. doi: 10.1126/scisignal.2005547.
9
A novel phosphatidic acid-protein-tyrosine phosphatase D2 axis is essential for ERBB2 signaling in mammary epithelial cells.一种新型的磷脂酸-蛋白酪氨酸磷酸酶D2轴对于乳腺上皮细胞中的ERBB2信号传导至关重要。
J Biol Chem. 2015 Apr 10;290(15):9646-59. doi: 10.1074/jbc.M114.627968. Epub 2015 Feb 13.
10
PTPN14 forms a complex with Kibra and LATS1 proteins and negatively regulates the YAP oncogenic function.蛋白酪氨酸磷酸酶非受体型14(PTPN14)与Kibra和大肿瘤抑制激酶1(LATS1)蛋白形成复合物,并负向调节Yes相关蛋白(YAP)的致癌功能。
J Biol Chem. 2014 Aug 22;289(34):23693-700. doi: 10.1074/jbc.M113.534701. Epub 2014 Jul 14.

KIBRA和PTPN14在Hippo信号通路及其他方面的调节作用

The Regulatory Role of KIBRA and PTPN14 in Hippo Signaling and Beyond.

作者信息

Wilson Kayla E, Yang Nuo, Mussell Ashley L, Zhang Jianmin

机构信息

Department of Cancer Genetics, Roswell Park Cancer Institute, Buffalo, NY 14263, USA.

出版信息

Genes (Basel). 2016 May 27;7(6):23. doi: 10.3390/genes7060023.

DOI:10.3390/genes7060023
PMID:27240404
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4929422/
Abstract

The Hippo signaling pathway regulates cellular proliferation and survival, thus exerting profound effects on normal cell fate and tumorigenesis. Pivotal effectors of this pathway are YAP/TAZ, transcriptional co-activators whose dysfunction contributes to the development of cancer. Complex networks of intracellular and extracellular signaling pathways that modulate YAP and TAZ activities have recently been identified. Among them, KIBRA and PTPN14 are two evolutionarily-conserved and important YAP/TAZ upstream regulators. They can negatively regulate YAP/TAZ functions separately or in concert. In this review, we summarize the current and emerging regulatory roles of KIBRA and PTPN14 in the Hippo pathway and their functions in cancer.

摘要

河马信号通路调节细胞增殖和存活,从而对正常细胞命运和肿瘤发生产生深远影响。该通路的关键效应因子是YAP/TAZ,即转录共激活因子,其功能失调会促进癌症的发展。最近已经确定了调节YAP和TAZ活性的细胞内和细胞外信号通路的复杂网络。其中,KIBRA和PTPN14是两个进化保守且重要的YAP/TAZ上游调节因子。它们可以单独或协同负向调节YAP/TAZ的功能。在本综述中,我们总结了KIBRA和PTPN14在河马通路中的当前和新出现的调节作用及其在癌症中的功能。