Evidence map›Paper›PMID 24246772›Full record

ArticleGynecologic oncology2014

Oncolytic measles and vesicular stomatitis virotherapy for endometrial cancer.

Yu-Ping Liu, Michael B Steele, Lukkana Suksanpaisan, Mark J Federspiel, Stephen J Russell, Kah Whye Peng, Jamie N Bakkum-Gamez

Open access · greenAbstract read
In one paragraph

Article in Gynecologic oncology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Measles Vaccine.Viral immunology · 2018
    Review
  13. Article
  14. Review
  15. Article
  16. [Advances in measles virus for cancer therapy].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2015
    Article
  17. Review
  18. Progress in oncolytic virotherapy for the treatment of thyroid malignant neoplasm.Journal of experimental & clinical cancer research : CR · 2014
    Review
  19. Review
  20. Article
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

7 authors at 1 institution in 1 country.

Yu-Ping LiuDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, USA.
Michael B SteeleDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, USA.
Lukkana SuksanpaisanDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, USA.
Mark J FederspielDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, USA; Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, USA.
Stephen J RussellDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, USA; Division of Hematology, Mayo Clinic, Rochester, MN, USA.
Kah Whye PengDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, USA; Division of Gynecology, Mayo Clinic, Rochester, MN, USA.
Jamie N Bakkum-GamezDivision of Gynecologic Surgery, Mayo Clinic, Rochester, MN, USA. Electronic address: bakkum.jamie@mayo.edu.
Mayo Clinic in Arizona · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI AKHILESH PANDEY · 1985 to 2026
$151.3M
Use of microfluidic tumor cultures to enable clinical trials of therapies for ovarian cancerP50CA136393 · NCI · MAYO CLINIC ROCHESTER · PI ELLEN L. GOODE · 2009 to 2026
$37.0M
Mayo Clinic Interdisciplinary Women's Health Research ProgramK12HD065987 · NICHD · MAYO CLINIC ROCHESTER · PI KANTARCI, KEJAL · 2010 to 2023
$6.7M
Optimizing Measles Virotherapy in the Treatment of Ovarian CancerR01CA136547 · NCI · MAYO CLINIC ROCHESTER · PI GALANIS, EVANTHIA, PENG, KAH-WHYE · 2009 to 2012
$2.0M
Enhancing localization of therapeutic viruses and cells to tumor sitesR01CA129193 · NCI · MAYO CLINIC ROCHESTER · PI PENG, KAH-WHYE · 2009 to 2014
$1.8M
NCI NIH HHS P30 CA015083NCI NIH HHS P30CA015083NCI NIH HHS P50 CA136393NCI NIH HHS R01 CA129193NCI NIH HHS R01CA129193NCI NIH HHS R01 CA136547NCI NIH HHS R01CA136547NCI NIH HHS SPORE P50CA136393NICHD NIH HHS K12 HD065987
6 · The paper itself

Abstract

objectiveCurrent adjuvant therapy for advanced-stage, recurrent, and high-risk endometrial cancer (EC) has not reduced mortality from this malignancy, and novel systemic therapies are imperative. Oncolytic viral therapy has been shown to be effective in the treatment of gynecologic cancers, and we investigated the in vitro and in vivo efficacy of the Edmonston strain of measles virus (MV) and vesicular stomatitis virus (VSV) on EC.

methodsHuman EC cell lines (HEC-1-A, Ishikawa, KLE, RL95-2, AN3 CA, ARK-1, ARK-2, and SPEC-2) were infected with Edmonston strain MV expressing the thyroidal sodium iodide symporter, VSV expressing either human or murine IFN-β, or recombinant VSV with a methionine deletion at residue 51 of the matrix protein and expressing the sodium iodide symporter. Xenografts of HEC-1-A and AN3 CA generated in athymic mice were treated with intratumoral MV or VSV or intravenous VSV.

resultsIn vitro, all cell lines were susceptible to infection and cell killing by all 3 VSV strains except KLE. In addition, the majority of EC cell lines were defective in their ability to respond to type I IFN. Intratumoral VSV-treated tumors regressed more rapidly than MV-treated tumors, and intravenous VSV resulted in effective tumor control in 100% of mice. Survival was significantly longer for mice treated with any of the 3 VSV strains compared with saline.

conclusionVSV is clearly more potent in EC oncolysis than MV. A phase 1 clinical trial of VSV in EC is warranted.

Indexed as

Measles virusVesicular stomatitis Indiana virusAnimalsCell Line, TumorEndometrial NeoplasmsFemaleHumansInterferon Type IMiceOncolytic VirotherapyInterferon Type I50% tissue culture infective doseCD46cluster of differentiation 46DMEMDulbecco Modified Eagle MediumECEdmonston strain MV expressing the thyroidal sodium iodide symporterendometrial cancerEndometrial cancerGFPgreen fluorescent proteinhIFNβhuman IFN-βintratumoralintravenousITIVLDLRlow density lipoprotein receptorM51 proteinmeasles virusMeasles virusmIFNβMOImultiplicity of infectionmurine IFN-βMVMV-NISNISno adverse event levelNOAELOncolytic virotherapyoncolytic virusOVPEpoliovirus receptor-related 4PVRL4qRTquantitative real-timeresidue 51 of the matrix proteinR-phycoerythrinsodium iodide symporterTCID(50)vesicular stomatitis virusVesicular stomatitis virusvesicular stomatitis virus expressing human IFN-βvesicular stomatitis virus expressing murine IFN-βvesicular stomatitis virus with a methionine deletion at residue 51 of the matrix protein and expressing the sodium iodide symporterVSVVSV-hIFNβVSV-M51-NISVSV-mIFNβ

Identifiers

PMID24246772
PMCPMC3946955
OpenAlexW2094998843

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.