Evidence map›Paper›PMID 20498137›Full record

ArticleCarcinogenesis2010

An unusual function of RON receptor tyrosine kinase as a transcriptional regulator in cooperation with EGFR in human cancer cells.

Hsiao-Sheng Liu, Pei-Yin Hsu, Ming-Derg Lai, Hong-Yi Chang, Chung-Liang Ho, Hong-Lin Cheng, Hsing-Ta Chen, Yan-Ju Lin, Tsung-Jung Wu, Tzong-Shin Tzai and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Carcinogenesis, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

30 citing papers in PubMed, 55 citations in OpenAlex.

  1. Review
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  16. Dietary restriction: could it be considered as speed bump on tumor progression road?Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Review
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  20. 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

11 authors at 3 institutions in 3 countries.

Hsiao-Sheng LiuInstitute of Basic Medical Sciences, National Cheng Kung University, Tainan, Taiwan.
Pei-Yin Hsu
Ming-Derg Lai
Hong-Yi Chang
Chung-Liang Ho
Hong-Lin Cheng
Hsing-Ta Chen
Yan-Ju Lin
Tsung-Jung Wu
Tzong-Shin Tzai
Nan-Haw Chow
Institute of Physiology and Basic Medicine · RUInstitute of Molecular Medicine · INNational Cheng Kung University · TW

Funding

DNA Hypermethylation in Breast CancerR01CA069065 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI HUANG, TIM H.-M. · 2002 to 2011
$2.4M
NCI NIH HHS R01 CA069065NCI NIH HHS R01CA 69065NCI NIH HHS U54CA11300
6 · The paper itself

Abstract

Homodimerization of RON (MST1R), a receptor tyrosine kinase, usually occurs in cells stimulated by a ligand and leads to the downstream activation of signaling pathways. Here we report that bladder cancer cells, in response to physiological stress, use an alternative mechanism for signaling activation. Time-course studies indicated that RON migrated directly from the membrane to the nucleus of bladder cancer cells in response to serum starvation. Biochemical and genetic studies implied that this nuclear internalization was complexed with epidermal growth factor receptor (EGFR) and required the docking of importins. In vivo analysis confirmed that nuclear RON was present in 38.4% (28/73) of primary bladder tumors. Chromatin immunoprecipitation (ChIP) on microarray analysis further revealed that this internalized complex bound to at least 134 target genes known to participate in three stress-responsive networks: p53, stress-activated protein kinase/c-jun N-terminal kinase and phosphatidylinositol 3-kinase/Akt. These findings suggest that RON, in a complex with EGFR, acts as a transcriptional regulator in response to acute disturbances (e.g. serum starvation) imposed on cancer cells. In an attempt to re-establish homeostasis, these cells bypass regular mechanisms required by ligand stimulation and trigger the RON-directed transcriptional response, which confers a survival advantage.

Indexed as

Transcription, GeneticBlotting, WesternCell DivisionDimerizationErbB ReceptorsGenes, ReporterHumansImmunohistochemistryKaryopherinsKineticsLuciferasesOligonucleotide Array Sequence AnalysisPolymerase Chain ReactionReceptor Protein-Tyrosine KinasesUrinary Bladder NeoplasmsErbB ReceptorsKaryopherinsLuciferasesReceptor Protein-Tyrosine KinasesRON protein

Identifiers

PMID20498137
PMCPMC2915629
OpenAlexW2146930964

What OpenQuestion holds

Textmetadata
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.