Evidence map›Paper›PMID 33884106›Full record

ArticleGenes & cancer2021

Immunotherapy of prostate cancer using novel synthetic DNA vaccines targeting multiple tumor antigens.

Devivasha Bordoloi, Peng Xiao, Hyeree Choi, Michelle Ho, Alfredo Perales-Puchalt, Makan Khoshnejad, J Joseph Kim, Laurent Humeau, Alagarsamy Srinivasan, David B Weiner and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Genes & cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. DNA-based immunotherapy for cancer: In vivo approaches for recalcitrant targets.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
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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

11 authors at 6 institutions in 3 countries.

Devivasha BordoloiVaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, PA, USA.
Peng XiaoVaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, PA, USA.
Hyeree ChoiVaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, PA, USA.
Michelle HoVaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, PA, USA.
Alfredo Perales-PuchaltVaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, PA, USA.
Makan KhoshnejadVaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, PA, USA.
J Joseph KimInovio Pharmaceuticals, Plymouth Meeting, PA, USA.
Laurent HumeauInovio Pharmaceuticals, Plymouth Meeting, PA, USA.
Alagarsamy SrinivasanNanoBio Diagnostics, West Chester, PA, USA.
David B WeinerVaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, PA, USA.
Kar MuthumaniVaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, PA, USA.
Holy Cross University · PLJan Kochanowski University · PLThe Wistar Institute · USInovio Pharmaceuticals (United States) · USKolon Life Science (South Korea) · KRMBio Diagnostics (United States) · US

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Luis J Montaner · 1985 to 2026
$75.9M
NCI NIH HHS P30 CA010815
6 · The paper itself

Abstract

Prostate cancer is a prevalent cancer in men and consists of both indolent and aggressive phenotypes. While active surveillance is recommended for the former, current treatments for the latter include surgery, radiation, chemo and hormonal therapy. It has been observed that the recurrence in the treated patients is high and results in castration resistant prostate cancer for which treatment options are limited. This scenario has prompted us to consider immunotherapy with synthetic DNA vaccines, as this approach can generate antigen-specific tumor-killing immune cells. Given the multifocal and heterogeneous nature of prostate cancer, we hypothesized that synthetic DNA vaccines targeting different prostate specific antigens are likely to induce broader and improved immunity who are at high risk as well as advanced clinical stage of prostate cancer, compared to a single antigen approach. Utilizing a bioinformatics approach, synthetic enhanced DNA vaccine (SEV) constructs were generated against STEAP1, PAP, PARM1, PSCA, PCTA and PSP94. Synthetic enhanced vaccines for prostate cancer antigens were shown to elicit antigen-specific immune responses in mice and the anti-tumor activity was evident in a prostate tumor challenge mouse model. These studies support further evaluation of the DNA tools for immunotherapy of prostate cancer and perhaps other cancers.

Indexed as

immune responsesprostate cancersynthetic DNA vaccines

Identifiers

PMID33884106
PMCPMC8045963
OpenAlexW3153374568

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.