Evidence map›Paper›PMID 27301426›Full record

ArticleScientific reports2016

Interaction of tRNA with MEK2 in pancreatic cancer cells.

Xiaoyun Wang, Christina R Chow, Kazumi Ebine, Jiyoung Lee, Marsha R Rosner, Tao Pan, Hidayatullah G Munshi

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. The dysregulation of tRNAs and tRNA derivatives in cancer.Journal of experimental & clinical cancer research : CR · 2018
    Review
  8. Review
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

7 authors at 2 institutions in 1 country.

Xiaoyun WangDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637, USA.
Christina R ChowDepartment of Medicine and the Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL 60611, USA.
Kazumi EbineDepartment of Medicine and the Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL 60611, USA.
Jiyoung LeeBen May Department for Cancer Research, University of Chicago, Chicago, IL 60637, USA.
Marsha R RosnerBen May Department for Cancer Research, University of Chicago, Chicago, IL 60637, USA.
Tao PanDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637, USA.
Hidayatullah G MunshiDepartment of Medicine and the Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL 60611, USA.
University of Chicago · USNorthwestern University · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
Mis-translation as a new mechanism of stress response in biologyDP1GM105386 · NIGMS · UNIVERSITY OF CHICAGO · PI PAN, TAO · 2012 to 2015
$3.1M
Targeting BET Bromodomain in Pancreatic CancerR01CA186885 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MUNSHI, HIDAYATULLAH G. · 2014 to 2017
$1.4M
NCI NIH HHS P30 CA060553NCI NIH HHS R01 CA186885NIGMS NIH HHS DP1 GM105386
6 · The paper itself

Abstract

Although the translational function of tRNA has long been established, extra translational functions of tRNA are still being discovered. We previously developed a computational method to systematically predict new tRNA-protein complexes and experimentally validated six candidate proteins, including the mitogen-activated protein kinase kinase 2 (MEK2), that interact with tRNA in HEK293T cells. However, consequences of the interaction between tRNA and these proteins remain to be elucidated. Here we tested the consequence of the interaction between tRNA and MEK2 in pancreatic cancer cell lines. We also generated disease and drug resistance-derived MEK2 mutants (Q60P, P128Q, S154F, E207K) to evaluate the function of the tRNA-MEK2 interaction. Our results demonstrate that tRNA interacts with the wild-type and mutant MEK2 in pancreatic cancer cells; furthermore, the MEK2 inhibitor U0126 significantly reduces the tRNA-MEK2 interaction. In addition, tRNA affects the catalytic activity of the wild type and mutant MEK2 proteins in different ways. Overall, our findings demonstrate the interaction of tRNA with MEK2 in pancreatic cancer cells and suggest that tRNA may impact MEK2 activity in cancer cells.

Indexed as

ButadienesCell Line, TumorHEK293 CellsHumansMAP Kinase Kinase 2MutationNitrilesPancreatic NeoplasmsRNA, TransferButadienesMAP2K2 protein, humanMAP Kinase Kinase 2NitrilesRNA, TransferU 0126

Identifiers

PMID27301426
PMCPMC4908586
OpenAlexW2437135116

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.