Evidence map›Paper›PMID 29920310›Full record

ArticleCellular signalling2018

Spatial regulation of signaling by the coordinated action of the protein tyrosine kinases MET and FER.

Jiali Zhang, Zuo Wang, Siwei Zhang, Yanxun Chen, Xuexue Xiong, Xiaojuan Li, Nicholas K Tonks, Gaofeng Fan

Abstract read
In one paragraph

Article in Cellular signalling, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 40% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Fer and FerT: A New Regulatory Link between Sperm and Cancer Cells.International journal of molecular sciences · 2023
    Review
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

Jiali ZhangSchool of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.
Zuo WangSchool of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.
Siwei ZhangCold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA; Department of Molecular Genetics and Microbiology, Stony Brook University, Stony Brook, NY 11794, USA.
Yanxun ChenFirst Affiliated Hospital, Fujian Medical University, Fuzhou 350005, China.
Xuexue XiongSchool of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.
Xiaojuan LiSchool of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.
Nicholas K TonksCold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA. Electronic address: tonks@cshl.edu.
Gaofeng FanSchool of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China; Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA. Electronic address: fangf@shanghaitech.edu.cn.
ShanghaiTech University · CNCold Spring Harbor Laboratory · USFujian Medical University · CNStony Brook University · US

Funding

Single-Cell Biology Shared ResourceP30CA045508 · NCI · COLD SPRING HARBOR LABORATORY · PI John Edward Moses · 1987 to 2026
$118.9M
PROTEIN TYROSINE DEPHOSPHORYLATION &SIGNAL TRANSDUCTIONR01CA053840 · NCI · COLD SPRING HARBOR LABORATORY · PI TONKS, NICHOLAS K · 1991 to 2025
$11.8M
Receptor PTPs, Cell Contract and Signal TransductionR01GM055989 · NIGMS · COLD SPRING HARBOR LABORATORY · PI TONKS, NICHOLAS K · 1997 to 2018
$6.7M
Protein Tyrosine Dephosphorylation &signal TransductionR37CA053840 · NCI · COLD SPRING HARBOR LABORATORY · PI TONKS, NICHOLAS K · 2001 to 2008
$5.2M
NCI NIH HHS P30 CA045508NCI NIH HHS R01 CA053840NCI NIH HHS R37 CA053840NIGMS NIH HHS R01 GM055989
6 · The paper itself

Abstract

A critical aspect of understanding the regulation of signal transduction is not only to identify the protein-protein interactions that govern assembly of signaling pathways, but also to understand how those pathways are regulated in time and space. In this report, we have applied both gain-of-function and loss-of-function analyses to assess the role of the non-receptor protein tyrosine kinase FER in activation of the HGF Receptor protein tyrosine kinase MET. Overexpression of FER led to direct phosphorylation of several signaling sites in MET, including Tyr1349, but not the activation loop residues Tyr1234/5; in contrast, suppression of FER by RNAi revealed that phosphorylation of both a C-terminal signaling site (Tyr1349) and the activation loop (Tyr1234/5) were influenced by the function of this kinase. Adaptin β, a component of the adaptor protein complex 2 (AP-2) that links clathrin to receptors in coated vesicles, was recruited to MET following FER-mediated phosphorylation. Furthermore, we provide evidence to support a role of FER in maintaining plasma membrane distribution of MET and thereby delaying protein-tyrosine phosphatase PTP1B-mediated inactivation of the receptor. Simultaneous up-regulation of FER and down-regulation of PTP1B observed in ovarian carcinoma-derived cell lines would be expected to contribute to persistent activation of HGF-MET signaling, suggesting that targeting of both FER and MET may be an effective strategy for therapeutic intervention in ovarian cancer.

Indexed as

CarcinomaCell LineCell Line, TumorCell MembraneDown-RegulationFemaleHEK293 CellsHumansOvarian NeoplasmsPhosphorylationProtein-Tyrosine KinasesProto-Oncogene Proteins c-metSignal TransductionUp-RegulationMET protein, humanProtein-Tyrosine Kinasesproto-oncogene protein c-fes-fpsProto-Oncogene Proteins c-metEndocytosisFERMETOvarian cancerPTP1B

Identifiers

PMID29920310
PMCPMC6530786
OpenAlexW2808971736

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.