Evidence map›Paper›PMID 30645971›Full record

ArticleCancer cell2019

The ERBB-STAT3 Axis Drives Tasmanian Devil Facial Tumor Disease.

Lindsay Kosack, Bettina Wingelhofer, Alexandra Popa, Anna Orlova, Benedikt Agerer, Bojan Vilagos, Peter Majek, Katja Parapatics, Alexander Lercher, Anna Ringler and 18 more

Open access · hybridAbstract read
In one paragraph

Article in Cancer cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
9.7field-weighted citation impact, top 1% 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

33 citing papers in PubMed, 54 citations in OpenAlex.

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  11. An HLA-G/SPAG9/STAT3 axis promotes brain metastases.Proceedings of the National Academy of Sciences of the United States of America · 2023
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  13. Inhibitor Library Screening of SH2 Domains Through Denaturation-Based Assays.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

28 authors at 6 institutions in 5 countries.

Lindsay KosackCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090 Vienna, Austria.
Bettina WingelhoferInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, 1210 Vienna, Austria.
Alexandra PopaCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090 Vienna, Austria.
Anna OrlovaInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, 1210 Vienna, Austria; Ludwig Boltzmann Institute for Cancer Research, 1090 Vienna, Austria.
Benedikt AgererCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090 Vienna, Austria.
Bojan VilagosCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090 Vienna, Austria.
Peter MajekCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090 Vienna, Austria.
Katja ParapaticsCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090 Vienna, Austria.
Alexander LercherCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090 Vienna, Austria.
Anna RinglerCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090 Vienna, Austria.
Johanna KlughammerCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090 Vienna, Austria.
Mark SmythCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090 Vienna, Austria.
Kseniya KhaminaCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090 Vienna, Austria.
Hatoon BaazimCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090 Vienna, Austria.
Elvin D de AraujoUniversity of Toronto, Mississauga, ON L5L 1C6, Canada.
David A RosaUniversity of Toronto, Mississauga, ON L5L 1C6, Canada.
Jisung ParkUniversity of Toronto, Mississauga, ON L5L 1C6, Canada.
Gary TinUniversity of Toronto, Mississauga, ON L5L 1C6, Canada.
Siawash AhmarUniversity of Toronto, Mississauga, ON L5L 1C6, Canada.
Patrick T GunningUniversity of Toronto, Mississauga, ON L5L 1C6, Canada.
Christoph BockCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090 Vienna, Austria; Department of Laboratory Medicine, Medical University of Vienna, 1090 Vienna, Austria; Max Planck Institute for Informatics, Saarland Informatics Campus, 66123 Saarbrücken, Germany.
Hannah V SiddleDepartment of Biological Science, University of Southampton, Southampton SO17 1BJ, UK.
Gregory M WoodsMenzies Institute for Medical Research, University of Tasmania, Hobart, TAS 7000, Australia.
Stefan KubicekCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090 Vienna, Austria.
Elizabeth P MurchisonTransmissible Cancer Group, Department of Veterinary Medicine, University of Cambridge, Cambridge CB3 0ES, UK.
Keiryn L BennettCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090 Vienna, Austria.
Richard MorigglInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, 1210 Vienna, Austria; Ludwig Boltzmann Institute for Cancer Research, 1090 Vienna, Austria; Medical University of Vienna, 1090 Vienna, Austria.
Andreas BergthalerCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090 Vienna, Austria. Electronic address: abergthaler@cemm.oeaw.ac.at.
Austrian Academy of Sciences · ATUniversity of Toronto · CAUniversity of Veterinary Medicine Vienna · ATUniversity of Cambridge · GBUniversity of Southampton · GBUniversity of Tasmania · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The marsupial Tasmanian devil (Sarcophilus harrisii) faces extinction due to transmissible devil facial tumor disease (DFTD). To unveil the molecular underpinnings of this transmissible cancer, we combined pharmacological screens with an integrated systems-biology characterization. Sensitivity to inhibitors of ERBB tyrosine kinases correlated with their overexpression. Proteomic and DNA methylation analyses revealed tumor-specific signatures linked to the evolutionary conserved oncogenic STAT3. ERBB inhibition blocked phosphorylation of STAT3 and arrested cancer cells. Pharmacological blockade of ERBB or STAT3 prevented tumor growth in xenograft models and restored MHC class I expression. This link between the hyperactive ERBB-STAT3 axis and major histocompatibility complex class I-mediated tumor immunosurveillance provides mechanistic insights into horizontal transmissibility and puts forward a dual chemo-immunotherapeutic strategy to save Tasmanian devils from DFTD. VIDEO ABSTRACT.

Indexed as

AnimalsDNA MethylationDrug Screening Assays, AntitumorErbB ReceptorsFacial NeoplasmsGene Expression Regulation, NeoplasticHistocompatibility Antigens Class IMarsupialiaMicePhosphorylationProteomicsSignal TransductionSmall Molecule LibrariesSTAT3 Transcription FactorXenograft Model Antitumor AssaysErbB ReceptorsHistocompatibility Antigens Class ISmall Molecule LibrariesSTAT3 Transcription FactorERBBhorizontal transmissionMHC class Ireceptor tyrosine kinasesSTAT3systems biologyTasmanian deviltransmissible cancertumor vulnerabilityxenograft

Identifiers

PMID30645971
PMCPMC6335503
OpenAlexW2953118656

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.