Evidence map›Paper›PMID 30554854›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2019

Engineered DNA Vaccination against Follicle-Stimulating Hormone Receptor Delays Ovarian Cancer Progression in Animal Models.

Alfredo Perales-Puchalt, Krzysztof Wojtak, Elizabeth K Duperret, Xue Yang, Anna M Slager, Jian Yan, Kar Muthumani, Luis J Montaner, David B Weiner

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
4.0field-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

22 citing papers in PubMed, 32 citations in OpenAlex.

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  12. Nucleic acid vaccination strategies for ovarian cancer.Frontiers in bioengineering and biotechnology · 2022
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  18. DEAD-Box Helicase 4 (Ddx4)International journal of molecular sciences · 2020
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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

9 authors at 2 institutions in 1 country.

Alfredo Perales-PuchaltVaccine and Immunotherapy Center, Microenvironment and Metastasis Program, The Wistar Institute, Philadelphia, PA 19104, USA.
Krzysztof WojtakVaccine and Immunotherapy Center, Microenvironment and Metastasis Program, The Wistar Institute, Philadelphia, PA 19104, USA.
Elizabeth K DuperretVaccine and Immunotherapy Center, Microenvironment and Metastasis Program, The Wistar Institute, Philadelphia, PA 19104, USA.
Xue YangVaccine and Immunotherapy Center, Microenvironment and Metastasis Program, The Wistar Institute, Philadelphia, PA 19104, USA.
Anna M SlagerInovio Pharmaceuticals, Plymouth Meeting, PA 19462, USA.
Jian YanInovio Pharmaceuticals, Plymouth Meeting, PA 19462, USA.
Kar MuthumaniVaccine and Immunotherapy Center, Microenvironment and Metastasis Program, The Wistar Institute, Philadelphia, PA 19104, USA.
Luis J MontanerVaccine and Immunotherapy Center, Microenvironment and Metastasis Program, The Wistar Institute, Philadelphia, PA 19104, USA.
David B WeinerVaccine and Immunotherapy Center, Microenvironment and Metastasis Program, The Wistar Institute, Philadelphia, PA 19104, USA. Electronic address: dweiner@wistar.org.
The Wistar Institute · USInovio Pharmaceuticals (United States) · US

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Nan Zhang · 1985 to 2026
$75.9M
TRAINING PROGRAM IN BASIC CANCER RESEARCHT32CA009171 · NCI · WISTAR INSTITUTE · PI Alessandro Gardini · 1985 to 2026
$15.3M
Targeted Combination Therapy for MelanomaP50CA174523 · NCI · WISTAR INSTITUTE · PI HERLYN, MEENHARD F · 2014 to 2018
$11.1M
Targeting hyaluronan in the tumor microenvironment to improve DNA vaccine immunotherapyF32CA213795 · NCI · WISTAR INSTITUTE · PI DUPERRET, ELIZABETH KENNEDY · 2017 to 2018
$94k
NCI NIH HHS F32 CA213795NCI NIH HHS P30 CA010815NCI NIH HHS P50 CA174523NCI NIH HHS T32 CA009171
6 · The paper itself

Abstract

Ovarian cancer presents in 80% of patients as a metastatic disease, which confers it with dismal prognosis despite surgery and chemotherapy. However, it is an immunogenic disease, and the presence of intratumoral T cells is a major prognostic factor for survival. We used a synthetic consensus (SynCon) approach to generate a novel DNA vaccine that breaks immune tolerance to follicle-stimulating hormone receptor (FSHR), present in 50% of ovarian cancers but confined to the ovary in healthy tissues. SynCon FSHR DNA vaccine generated robust CD8

Indexed as

AnimalsCancer VaccinesFemaleFlow CytometryHEK293 CellsHumansImmunoblottingImmunotherapyMiceOvarian NeoplasmsReceptors, FSHVaccines, DNACancer VaccinesReceptors, FSHVaccines, DNAcancer vaccineDNA vaccinefollicle-stimulating hormone receptorimmunotherapyovarian cancer

Identifiers

PMID30554854
PMCPMC6369450
OpenAlexW2905522371

What OpenQuestion holds

Textmetadata
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.