Evidence map›Paper›PMID 26272026›Full record

ArticleCancer gene therapy2015

Inhibition of the Aurora A kinase augments the anti-tumor efficacy of oncolytic measles virotherapy.

I D Iankov, C B Kurokawa, A B D'Assoro, J N Ingle, E Domingo-Musibay, C Allen, C M Crosby, A A Nair, M C Liu, I Aderca and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer gene therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Mitotic Poisons in Research and Medicine.Molecules (Basel, Switzerland) · 2020
    Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Potential and clinical translation of oncolytic measles viruses.Expert opinion on biological therapy · 2017
    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

12 authors at 2 institutions in 1 country.

I D IankovDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, USA.
C B KurokawaDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, USA.
A B D'AssoroDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, USA.
J N IngleDepartment of Oncology, Mayo Clinic, Rochester, MN, USA.
E Domingo-MusibayDepartment of Oncology, Mayo Clinic, Rochester, MN, USA.
C AllenDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, USA.
C M CrosbyDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, USA.
A A NairDepartment of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
M C LiuDepartment of Oncology, Mayo Clinic, Rochester, MN, USA.
I AdercaDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, USA.
M J FederspielDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, USA.
E GalanisDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, USA.
Mayo Clinic in Arizona · USMayo Clinic in Florida · US

Funding

The Role of CHFR in Tumorigenesis and Paclitaxel-Sensitivity in Breast CancerP50CA116201 · NCI · MAYO CLINIC ROCHESTER · PI PETER C LUCAS · 2005 to 2026
$49.9M
Optimizing Measles Virotherapy in the Treatment of Ovarian CancerR01CA136547 · NCI · MAYO CLINIC ROCHESTER · PI GALANIS, EVANTHIA, PENG, KAH-WHYE · 2009 to 2012
$2.0M
Measles Virotherapy and radiovirotherapy in the Treatment of recurrent gliomasR01CA154348 · NCI · MAYO CLINIC ROCHESTER · PI GALANIS, EVANTHIA · 2011 to 2014
$1.3M
NCI NIH HHS P50 CA116201NCI NIH HHS P50CA 116201NCI NIH HHS R01 CA136547NCI NIH HHS R01CA 136547NCI NIH HHS R01 CA154348NCI NIH HHS R01CA 154348
6 · The paper itself

Abstract

Oncolytic measles virus (MV) strains have demonstrated broad spectrum preclinical anti-tumor efficacy, including breast cancer. Aurora A kinase controls mitotic spindle formation and has a critical role in malignant transformation. We hypothesized that the Aurora A kinase inhibitor MLN8237 (alisertib) can increase MV oncolytic effect and efficacy by causing mitotic arrest. Alisertib enhanced MV oncolysis in vitro and significantly improved outcome in vivo against breast cancer xenografts. In a disseminated MDA-231-lu-P4 lung metastatic model, the MV/alisertib combination treatment markedly increased median survival to 82.5 days with 20% of the animals being long-term survivors versus 48 days median survival for the control animals. Similarly, in a pleural effusion model of advanced breast cancer, the MV/alisertib combination significantly improved outcome with a 74.5 day median survival versus the single agent groups (57 and 40 days, respectively). Increased viral gene expression and IL-24 upregulation were demonstrated, representing possible mechanisms for the observed increase in anti-tumor effect. Inhibiting Aurora A kinase with alisertib represents a novel approach to enhance MV-mediated oncolysis and antitumor effect. Both oncolytic MV strains and alisertib are currently tested in clinical trials, this study therefore provides the basis for translational applications of this combinatorial strategy in the treatment of patients with advanced breast cancer.

Indexed as

Measles virusOncolytic VirotherapyAdenocarcinomaAnimalsAntineoplastic AgentsAurora Kinase BAzepinesBacterial ProteinsBreast NeoplasmsChlorocebus aethiopsCombined Modality TherapyFemaleGene Expression RegulationHumansImmunoglobulin lambda-ChainsInterleukin-24Antineoplastic AgentsAURKB protein, humanAurora Kinase BAzepinesBacterial ProteinsImmunoglobulin lambda-ChainsInterleukin-24InterleukinsMLN 8237neutrophil-activating protein A, Helicobacter pyloriProtein Kinase InhibitorsPyrimidines

Identifiers

PMID26272026
PMCPMC4589445
OpenAlexW1787451882

What OpenQuestion holds

Textmetadata
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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.