Evidence map›Paper›PMID 26779809›Full record

ArticleOncogenesis2016

Uncoupling of EGFR-RAS signaling and nuclear localization of YBX1 in colorectal cancer.

F Roßner, C Gieseler, M Morkel, H-D Royer, M Rivera, H Bläker, M Dietel, R Schäfer, C Sers

Open access · goldAbstract read
In one paragraph

Article in Oncogenesis, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. o8G-modified circKIAA1797 promotes lung cancer development by inhibiting cuproptosis.Journal of experimental & clinical cancer research : CR · 2025
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  6. 5-Methylcytosine (mFrontiers in immunology · 2022
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  8. C1222C Deletion in Exon 8 ofFrontiers in oncology · 2020
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. 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

9 authors at 4 institutions in 1 country.

F RoßnerInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin, Germany.
C GieselerInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin, Germany.
M MorkelInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin, Germany.
H-D RoyerInstitute of Human Genetics and Anthropology, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
M RiveraEPO, Experimental Pharmacology & Oncology Berlin-Buch GmbH, Berlin, Germany.
H BläkerInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin, Germany.
M DietelInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin, Germany.
R SchäferInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin, Germany.
C SersInstitute of Pathology, Charité Universitätsmedizin Berlin, Berlin, Germany.
Charité - Universitätsmedizin Berlin · DEGerman Cancer Research Center · DEHeidelberg University · DEHeinrich Heine University Düsseldorf · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transcription factor YBX1 can act as a mediator of signals transmitted via the EGFR-RAS-MAPK axis. YBX1 expression has been associated with tumor progression and prognosis in multiple types of cancer. Immunohistochemical studies have revealed dependency between YBX1 expression and individual EGFR family members. We analyzed YBX1 and EGFR family proteins in a colorectal cancer (CRC) cohort and provide functional analyses of YBX1 in the context of EGFR-RAS-MAPK signaling. Immunohistochemistry for YBX1 and EGFR family receptors with two antibodies for YBX1 and EGFR were performed and related to clinicopathological data. We employed Caco2 cells expressing an inducible KRASV12 gene to determine effects on localization and levels of YBX1. Mouse xenografts of Caco2-KRASV12 cells were used to determine YBX1 dynamics in a tissue context. The two different antibodies against YBX1 showed discordant immunohistochemical stainings in cell culture and clinical specimens. Expression of YBX1 and EGFR family members were not correlated in CRC. Analysis of Caco2 xenografts displayed again heterogeneity of YBX1 staining with both antibodies. Our results suggest that YBX1 is controlled via complex regulatory mechanisms involving tumor stroma interaction and signal transduction processes. Our study highlights that YBX1 antibodies have different specificities, advocating their use in a combined manner.

Identifiers

PMID26779809
PMCPMC4728680
OpenAlexW2340379245

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.