Evidence map›Paper›PMID 30044378›Full record

ArticleCancers2018

Activation of ERBB4 in Glioblastoma Can Contribute to Increased Tumorigenicity and Influence Therapeutic Response.

Jacqueline F Donoghue, Lauren T Kerr, Naomi W Alexander, Sameer A Greenall, Anthony B Longano, Nicholas G Gottardo, Rong Wang, Viviane Tabar, Timothy E Adams, Paul S Mischel and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
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  11. Observational
  12. Receptor Tyrosine Kinase Signaling and Targeting in Glioblastoma Multiforme.International journal of molecular sciences · 2021
    Review
  13. The role of ErbB4 in cancer.Cellular oncology (Dordrecht, Netherlands) · 2020
    Review
  14. Article
  15. Article
  16. Article
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  19. 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 8 institutions in 2 countries.

Jacqueline F DonoghueOncogenic Signalling Group, Hudson Institute of Medical Research, 21⁻37 Wright Street, Clayton, VIC 3168, Australia. jacqueline.donoghue@unimelb.edu.au.
Lauren T KerrOncogenic Signalling Group, Hudson Institute of Medical Research, 21⁻37 Wright Street, Clayton, VIC 3168, Australia. Lauren.Kerr@cancer.org.uk.
Naomi W AlexanderTelethon Kids Cancer Centre, Telethon Kids Institute, University of Western Australia, Perth, WA 6008, Australia. naomi.alexander@telethonkids.org.au.
Sameer A GreenallOncogenic Signalling Group, Hudson Institute of Medical Research, 21⁻37 Wright Street, Clayton, VIC 3168, Australia. sameer.greenall@hudson.org.au.
Anthony B LonganoDepartment of Anatomical Pathology, Monash Medical Centre, Clayton, VIC 3168, Australia. anthony.longano@monashhealth.org.
Nicholas G GottardoTelethon Kids Cancer Centre, Telethon Kids Institute, University of Western Australia, Perth, WA 6008, Australia. Nicholas.Gottardo@telethonkids.org.au.
Rong WangDepartment of Neurosurgery and Center for Stem Cell Biology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA. wangr@mskcc.org.
Viviane TabarDepartment of Neurosurgery and Center for Stem Cell Biology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA. tabarv@mskcc.org.
Timothy E AdamsBiomedical Manufacturing, Commonwealth Scientific and Industrial Research Organisation (CSIRO), Parkville, VIC 3052, Australia. Tim.Adams@csiro.au.
Paul S MischelLudwig Institute for Cancer Research, University of California San Diego, La Jolla, CA 92093, USA. pmischel@ucsd.edu.
Terrance G JohnsOncogenic Signalling Group, Hudson Institute of Medical Research, 21⁻37 Wright Street, Clayton, VIC 3168, Australia. Terrance.Johns@telethonkids.org.au.
Monash University · AUMemorial Sloan Kettering Cancer Center · USCommonwealth Scientific and Industrial Research Organisation · AUHudson Institute of Medical Research · AUMonash Medical Centre · AUThe Kids Research Institute Australia · AUUniversity of California, San Diego · USUniversity of Western Australia · AU

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
The role of mTORC2 in reprogramming cancer cell metabolismR01NS073831 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MISCHEL, PAUL S · 2011 to 2020
$3.4M
NCI NIH HHS P30 CA008748NINDS NIH HHS R01 NS073831
6 · The paper itself

Abstract

Glioblastoma (GBM) is often resistant to conventional and targeted therapeutics. ErbB2 Receptor Tyrosine Kinase 4 (ERBB4) is expressed throughout normal brain and is an oncogene in several pediatric brain cancers; therefore, we investigated ERBB4 as a prognostic marker and therapeutic target in GBM. Using RT-qPCR, we quantified mRNA encoding total ERBB4 and known ERBB4 variants in GBM and non-neoplastic normal brain (NNB) samples. Using immunohistochemistry, we characterized the localization of total and phosphorylated ERBB4 (p-ERBB4) and EGFR protein in archived GBM samples and assessed their association with patient survival. Furthermore, we evaluated the effect of ERBB4 phosphorylation on angiogenesis and tumorigenicity in GBM xenograft models. Total

Indexed as

EGFRERBB4GBMprognosistherapy

Identifiers

PMID30044378
PMCPMC6116191
OpenAlexW2808159589

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.