Evidence map›Paper›PMID 21989183›Full record

ArticleBritish journal of cancer2011

Photodynamic therapy augments the efficacy of oncolytic vaccinia virus against primary and metastatic tumours in mice.

M Gil, M Bieniasz, M Seshadri, D Fisher, M J Ciesielski, Y Chen, R K Pandey, D Kozbor

Open access · bronzeAbstract read
In one paragraph

Article in British journal of cancer, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.6field-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

32 citing papers in PubMed, 46 citations in OpenAlex.

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  11. Viral Nanoparticle System: An Effective Platform for Photodynamic Therapy.International journal of molecular sciences · 2021
    Review
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  18. Improved micro-distribution of antibody-photon absorber conjugates after initial near infrared photoimmunotherapy (NIR-PIT).Journal of controlled release : official journal of the Controlled Release Society · 2016
    Article
  19. Article
  20. Review
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

8 authors at 1 institution in 1 country.

M GilDepartment of Immunology, Roswell Park Cancer Institute, Buffalo, NY 14263, USA.
M Bieniasz
M Seshadri
D Fisher
M J Ciesielski
Y Chen
R K Pandey
D Kozbor
Roswell Park Comprehensive Cancer Center · US

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MARK G FRATTINI · 1985 to 2026
$116.6M
StatisticsP01CA055791 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI GOLLNICK, SANDRA O. · 1992 to 2019
$36.0M
Gene Delivery Systems of Carbohydrate Mimotopes to Dendritic CellsR21EB008071 · NIBIB · ROSWELL PARK CANCER INSTITUTE CORP · PI KOZBOR, DANUTA B · 2008 to 2009
$483k
Enhancing Efficacy of Oncolytic Viriotherapy with PDTR21CA140886 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI KOZBOR, DANUTA B · 2010 to 2011
$441k
NCI NIH HHS CA140886NCI NIH HHS CA16056NCI NIH HHS CA55791NCI NIH HHS P01 CA055791NCI NIH HHS P30 CA016056NCI NIH HHS R21 CA140886NIBIB NIH HHS EB008071NIBIB NIH HHS R21 EB008071
6 · The paper itself

Abstract

backgroundTherapies targeted towards the tumour vasculature can be exploited for the purpose of improving the systemic delivery of oncolytic viruses to tumours. Photodynamic therapy (PDT) is a clinically approved treatment for cancer that is known to induce potent effects on tumour vasculature. In this study, we examined the activity of PDT in combination with oncolytic vaccinia virus (OVV) against primary and metastatic tumours in mice.

methodsThe effect of 2-[1-hexyloxyethyl-]-2-devinyl pyropheophorbide-a (HPPH)-sensitised-PDT on the efficacy of oncolytic virotherapy was investigated against subcutaneously implanted syngeneic murine NXS2 neuroblastoma and human FaDu head and neck squamous cell carcinoma xenografts in nude mice. Treatment efficacy was evaluated by monitoring tumour growth and survival. The effects of combination treatment on vascular function were examined using magnetic resonance imaging (MRI) and immunohistochemistry, whereas viral replication in tumour cells was analysed by a standard plaque assay. Normal tissue phototoxicity following PDT-OV treatment was studied using the mouse foot response assay.

resultsCombination of PDT with OVV resulted in inhibition of primary and metastatic tumour growth compared with either monotherapy. PDT-induced vascular disruption resulted in higher intratumoural viral titres compared with the untreated tumours. Five days after delivery of OVV, there was a loss of blood flow to the interior of tumour that was associated with infiltration of neutrophils. Administration of OVV did not result in any additional photodynamic damage to normal mouse foot tissue.

conclusionThese results provide evidence into the usefulness of PDT as a means of enhancing intratumoural replication and therapeutic efficacy of OV.

Indexed as

Oncolytic VirotherapyVaccinia virusAnimalsFemaleFlow CytometryHumansImmunohistochemistryMagnetic Resonance ImagingMiceMice, NudeNeoplasm MetastasisNeoplasms, ExperimentalVirus ReplicationXenograft Model Antitumor Assays

Identifiers

PMID21989183
PMCPMC3242530
OpenAlexW2059585528

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.