Evidence map›Paper›PMID 24474587›Full record

ArticleInternational journal of cancer2014

Oncolytic vaccinia virus demonstrates antiangiogenic effects mediated by targeting of VEGF.

Weizhou Hou, Hannah Chen, Juan Rojas, Padma Sampath, Stephen H Thorne

Abstract read
In one paragraph

Article in International journal of cancer, 2014. 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
2.8field-weighted citation impact, top 10% 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, 59 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Personalizing Oncolytic Immunovirotherapy Approaches.Molecular diagnosis & therapy · 2024
    Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Virus-inspired strategies for cancer therapy.Seminars in cancer biology · 2022
    Review
  18. 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

5 authors at 1 institution in 1 country.

Weizhou HouDepartment of Surgery, University of Pittsburgh Cancer Institute, University of Pittsburgh, PA.
Hannah Chen
Juan Rojas
Padma Sampath
Stephen H Thorne
UPMC Hillman Cancer Center · US

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JOHN C. BYRD · 1988 to 2026
$158.0M
Enhancing Delivery and Regulating Gene Expression in Oncolytic Vaccinia VectorsR01CA140215 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI THORNE, STEPHEN H · 2010 to 2014
$1.5M
NCI NIH HHS P30 CA047904NCI NIH HHS P30 CA047904-21S3NCI NIH HHS R01 CA140215
6 · The paper itself

Abstract

Oncolytic vaccinia virus has been shown to induce a profound, rapid and tumor-specific vascular collapse in both preclinical models and clinical studies; however, a complete examination of the kinetics and levels of collapse and revascularization has not been described previously. Contrast-enhanced ultrasound was used to follow tumor perfusion levels in mouse tumor models at times after vaccinia therapy. It was observed that revascularization after viral therapy was dramatically delayed and did not occur until after viral clearance. This indicated that oncolytic vaccinia may possess a previously undescribed antiangiogenic potential that might synergize with the reported anti-vascular effects. Despite a rapid loss of perfusion and widespread hypoxia within the tumor, it was observed that VEGF levels in the tumor were suppressed throughout the period of active viral infection. Although tumor vasculature could eventually reform after the viral therapy was cleared in mouse models, anti-tumor effects could be significantly enhanced through additional combination with anti-VEGF therapies. This was initially examined using a gene therapy approach (Ad-Flk1-Fc) to target VEGF directly, demonstrating that the timing of application of the antiangiogenic therapy was critical. However, it is also known that oncolytic vaccinia sensitizes tumors to tyrosine kinase inhibitors (TKI) in the clinic through an unknown mechanism. It is possible this phenomenon may be mediated through the antiangiogenic effects of the TKIs. This was modeled in mouse tumors using sunitinib in combination with oncolytic vaccinia. It was observed that prevention of angiogenesis mediated by oncolytic vaccinia can be utilized to enhance the TKI therapy.

Indexed as

Oncolytic VirusesVaccinia virusAngiogenesis InhibitorsAnimalsCell Line, TumorDrug Resistance, NeoplasmEnzyme InhibitorsGenetic TherapyHumansIndolesMiceMice, Inbred BALB CMice, NudeNeoplasmsNeovascularization, PathologicOncolytic VirotherapyAngiogenesis InhibitorsEnzyme InhibitorsIndolesProtein-Tyrosine KinasesPyrrolesSunitinibVascular Endothelial Growth Factor Avascular endothelial growth factor A, mouseantiangiogenicanti-vascularoncolytic virustyrosine kinase inhibitorVEGF

Identifiers

PMID24474587
PMCPMC4061259
OpenAlexW1768741830

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.