Evidence map›Paper›PMID 27626672›Full record

ArticleCell reports2016

Drosophila Cancer Models Identify Functional Differences between Ret Fusions.

Sarah Levinson, Ross L Cagan

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

36 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Modelling Cancer in Drosophila: Exploration to Personalised Medicine.Advances in experimental medicine and biology · 2025
    Review
  5. Review
  6. Article
  7. CCDC6-RET fusion protein regulates Ras/MAPK signaling through the fusion- GRB2-SHC1 signal niche.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Frontiers in oncology · 2022
    Review
  15. Frontiers in genetics · 2022
    Review
  16. Review
  17. Article
  18. Review
  19. Review
  20. Iron and Cancer: 2020 Vision.Cancer research · 2020
    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

2 authors at 1 institution in 1 country.

Sarah LevinsonDepartment of Developmental and Regenerative Biology and Graduate School of Biomedical Sciences, Icahn School of Medicine at Mount Sinai, One Gustave Levy Place, New York, NY 10029-1020, USA.
Ross L CaganDepartment of Developmental and Regenerative Biology and Graduate School of Biomedical Sciences, Icahn School of Medicine at Mount Sinai, One Gustave Levy Place, New York, NY 10029-1020, USA. Electronic address: ross.cagan@mssm.edu.
Icahn School of Medicine at Mount Sinai · US

Funding

A New Disease Platform Leveraging Complex Drosophila and Mammalian ModelsU54OD020353 · OD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CAGAN, ROSS LEIGH · 2015 to 2019
$10.3M
A Drosophila Model for Src-Mediated OncogenesisR01CA109730 · NCI · WASHINGTON UNIVERSITY · PI CAGAN, ROSS LEIGH · 2004 to 2013
$2.9M
A Drosophila Model Linking Diet-induced Obesity and Cancer (PQ 1)R01CA170495 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CAGAN, ROSS LEIGH · 2012 to 2015
$1.4M
Drosophila models of Ret fusions in Papillary Thyroid CarcinomaF31CA189794 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI LEVINSON, SARAH · 2014 to 2015
$71k
NCI NIH HHS F31 CA189794NCI NIH HHS R01 CA109730NCI NIH HHS R01 CA170495NIH HHS U54 OD020353
6 · The paper itself

Abstract

We generated and compared Drosophila models of RET fusions CCDC6-RET and NCOA4-RET. Both RET fusions directed cells to migrate, delaminate, and undergo EMT, and both resulted in lethality when broadly expressed. In all phenotypes examined, NCOA4-RET was more severe than CCDC6-RET, mirroring their effects on patients. A functional screen against the Drosophila kinome and a library of cancer drugs found that CCDC6-RET and NCOA4-RET acted through different signaling networks and displayed distinct drug sensitivities. Combining data from the kinome and drug screens identified the WEE1 inhibitor AZD1775 plus the multi-kinase inhibitor sorafenib as a synergistic drug combination that is specific for NCOA4-RET. Our work emphasizes the importance of identifying and tailoring a patient's treatment to their specific RET fusion isoform and identifies a multi-targeted therapy that may prove effective against tumors containing the NCOA4-RET fusion.

Indexed as

AnimalsCell MovementDisease Models, AnimalDrosophila melanogasterDrug SynergismEpithelial-Mesenchymal TransitionNeoplasmsOncogene Proteins, FusionProtein Kinase InhibitorsProto-Oncogene Proteins c-retUp-RegulationOncogene Proteins, FusionProtein Kinase InhibitorsProto-Oncogene Proteins c-ret

Identifiers

PMID27626672
PMCPMC5858711
OpenAlexW2520810168

What OpenQuestion holds

Textmetadata
LicenceTDM
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.