Evidence map›Paper›PMID 18084242›Full record

ArticleCancer gene therapy2008

Oncolytic virotherapy for ovarian carcinomatosis using a replication-selective vaccinia virus armed with a yeast cytosine deaminase gene.

S Chalikonda, M H Kivlen, M E O'Malley, X D Eric Dong, J A McCart, M C Gorry, X-Y Yin, C K Brown, H J Zeh, Z S Guo and 1 more

Open access · greenAbstract read
In one paragraph

Article in Cancer gene therapy, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

44 citing papers in PubMed, 73 citations in OpenAlex.

  1. Review
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  11. Optimizing oncolytic virotherapy in cancer treatment.Nature reviews. Drug discovery · 2019
    Review
  12. Progress in gene therapy using oncolytic vaccinia virus as vectors.Journal of cancer research and clinical oncology · 2018
    Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Phase 1 Study of Intravenous Oncolytic Poxvirus (vvDD) in Patients With Advanced Solid Cancers.Molecular therapy : the journal of the American Society of Gene Therapy · 2016
    Article
  18. Article
  19. Article
  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

11 authors at 4 institutions in 2 countries.

S ChalikondaDepartment of Surgery, University of Pittsburgh Cancer Institute, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
M H Kivlen
M E O'Malley
X D Eric Dong
J A McCart
M C Gorry
X-Y Yin
C K Brown
H J Zeh
Z S Guo
D L Bartlett
University of Pittsburgh · USNational Cancer Institute · USUPMC Hillman Cancer Center · USSun Yat-sen University · CN

Funding

Development of a Tumor Selective Replicating VacciniaR01CA100415 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BARTLETT, DAVID L · 2004 to 2007
$1.2M
Intramural NIH HHSNCI NIH HHS CA100415NCI NIH HHS R01 CA100415
6 · The paper itself

Abstract

In this study, we assessed the ability of a highly tumor-selective oncolytic vaccinia virus armed with a yeast cytosine deaminase gene to infect and lyse human and murine ovarian tumors both in vitro and in vivo. The virus vvDD-CD could infect, replicate in and effectively lyse both human and mouse ovarian cancer cells in vitro. In two different treatment schedules involving either murine MOSEC or human A2780 ovarian carcinomatosis models, regional delivery of vvDD-CD selectively targeted tumor cells and ovarian tissue, effectively delaying the development of either tumor or ascites and leading to significant survival advantages. Oncolytic virotherapy using vvDD-CD in combination with the prodrug 5-fluorocytosine conferred an additional long-term survival advantage upon tumor-bearing immunocompetent mice. These findings demonstrate that a tumor-selective oncolytic vaccinia combined with gene-directed enzyme prodrug therapy is a highly effective strategy for treating advanced ovarian cancers in both syngeneic mouse and human xenograft models. Given the biological safety, tumor selectivity and oncolytic potency of this armed oncolytic virus, this dual therapy merits further investigation as a promising new treatment for metastatic ovarian cancer.

Indexed as

Oncolytic VirotherapyVirus ReplicationAnimalsAntimetabolitesCarcinomaCell Line, TumorCombined Modality TherapyCytosine DeaminaseFemaleFlucytosineHumansMiceMice, Inbred C57BLMice, NudeOvarian NeoplasmsSaccharomyces cerevisiaeAntimetabolitesCytosine DeaminaseFlucytosine

Identifiers

PMID18084242
PMCPMC2975702
OpenAlexW2023833567

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.