Evidence map›Paper›PMID 23928059›Full record

ArticleMolecular cancer research : MCR2013

Dynamic and nuclear expression of PDGFRα and IGF-1R in alveolar Rhabdomyosarcoma.

M Imran Aslam, Simone Hettmer, Jinu Abraham, Dorian Latocha, Anuradha Soundararajan, Elaine T Huang, Martin W Goros, Joel E Michalek, Shuyu Wang, Atiya Mansoor and 4 more

Open access · greenAbstract read
In one paragraph

Article in Molecular cancer research : MCR, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.1field-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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Extreme Diversity of the Human Vascular Mesenchymal Cell Landscape.Journal of the American Heart Association · 2020
    Pooled it
  2. IGF-1R targeting in cancer - does sub-cellular localization matter?Journal of experimental & clinical cancer research : CR · 2023
    Review
  3. Article
  4. Molecularly Defined Subsets of Ewing Sarcoma Tumors Differ in Their Responses to IGF1R and WEE1 Inhibition.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
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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

14 authors at 5 institutions in 1 country.

M Imran AslamOregon Health & Science University, 3181 SW Sam Jackson Park Rd., MC-L321, Portland, OR 97239. keller@ohsu.edu.
Simone Hettmer
Jinu Abraham
Dorian Latocha
Anuradha Soundararajan
Elaine T Huang
Martin W Goros
Joel E Michalek
Shuyu Wang
Atiya Mansoor
Brian J Druker
Amy J Wagers
Jeffrey W Tyner
Charles Keller
Howard Hughes Medical Institute · USDana-Farber Cancer Institute · USOregon Health & Science University · USThe University of Texas Health Science Center at San Antonio · USHarvard Stem Cell Institute · US

Funding

Therapeutic Targets in Alveolar RhabdomyosarcomaR01CA133229 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI KELLER, CHARLES · 2008 to 2012
$1.9M
Howard Hughes Medical InstituteNCI NIH HHS 5R01CA133229-05NCI NIH HHS R01 CA133229
6 · The paper itself

Abstract

unlabelledSince the advent of tyrosine kinase inhibitors as targeted therapies in cancer, several receptor tyrosine kinases (RTK) have been identified as operationally important for disease progression. Rhabdomyosarcoma (RMS) is a malignancy in need of new treatment options; therefore, better understanding of the heterogeneity of RTKs would advance this goal. Here, alveolar RMS (aRMS) tumor cells derived from a transgenic mouse model expressing two such RTKs, platelet-derived growth factor (PDGFR)α and insulin-like growth factor (IGF)-1R, were investigated by fluorescence-activated cell sorting (FACS). Sorted subpopulations that were positive or negative for PDGFRα and IGF-1R dynamically altered their cell surface RTK expression profiles as early as the first cell division. Interestingly, a difference in total PDGFRα expression and nuclear IGF-1R expression was conserved in populations. Nuclear IGF-1R expression was greater than cytoplasmic IGF-1R in cells with initially high cell surface IGF-1R, and cells with high nuclear IGF-1R established tumors more efficiently in vivo. RNA interference-mediated silencing of IGF-1R in the subpopulation of cells initially harboring higher cell surface and total IGF-1R resulted in significantly reduced anchorage-independent colony formation as compared with cells with initially lower cell surface and total IGF-1R expression. Finally, in accordance with the findings observed in murine aRMS, human aRMS also had robust expression of nuclear IGF-1R. IMPLICATIONS: RTK expression status and subcellular localization dynamics are important considerations for personalized medicine.

Indexed as

AnimalsCell Line, TumorCell NucleusDisease Models, AnimalFlow CytometryGene Expression Regulation, NeoplasticHumansImmunohistochemistryMiceMice, SCIDMice, TransgenicReceptor, IGF Type 1Receptor, Platelet-Derived Growth Factor alphaRhabdomyosarcoma, AlveolarTissue Array AnalysisReceptor, IGF Type 1Receptor, Platelet-Derived Growth Factor alpha

Identifiers

PMID23928059
PMCPMC3834004
OpenAlexW2101493381

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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.