Evidence map›Paper›PMID 21712815›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2011

Oncolytic adenovirus expressing soluble TGFβ receptor II-Fc-mediated inhibition of established bone metastases: a safe and effective systemic therapeutic approach for breast cancer.

Zebin Hu, Helen Gerseny, Zhenwei Zhang, Yun-Ju Chen, Arthur Berg, Zhiling Zhang, Stuart Stock, Prem Seth

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Genetic Modifications That Expand Oncolytic Virus Potency.Frontiers in molecular biosciences · 2022
    Review
  6. Review
  7. Beyond cancer cells: Targeting the tumor microenvironment with gene therapy and armed oncolytic virus.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Transforming growth factor-β: A therapeutic target for cancer.Human vaccines & immunotherapeutics · 2017
    Review
  16. Article
  17. Article
  18. Article
  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

8 authors at 2 institutions in 1 country.

Zebin HuGene Therapy Program, Department of Medicine, NorthShore Research Institute, University of Chicago, Evanston, Illinois 60201, USA.
Helen Gerseny
Zhenwei Zhang
Yun-Ju Chen
Arthur Berg
Zhiling Zhang
Stuart Stock
Prem Seth
NorthShore University HealthSystem · USNorthwestern University · US

Funding

Oncolytic Adenovirus-sTGFbetaRIIFc Targeting Breast Cancer Bone MetastasisR01CA127380 · NCI · NORTHSHORE UNIVERSITY HEALTHSYSTEM · PI SETH, PREM · 2007 to 2011
$1.4M
NCI NIH HHS R01CA12738NCI NIH HHS R01 CA127380
6 · The paper itself

Abstract

In recent years, oncolytic adenoviruses have shown some promise as a novel class of antitumor agents. However, their utility in targeting bone metastases is relatively less studied. We have examined whether the systemic therapy of oncolytic adenoviruses expressing the soluble form of transforming growth factor-β (TGFβ) receptor II fused with human immunoglobulin G1 can be developed for the treatment of established breast cancer bone metastases. MDA-MB-231-luc2 human breast cancer cells were injected in the left heart ventricle of nude mice to establish bone metastasis. Mice with hind limb tumors were administered (on days 8 and 11) oncolytic adenoviruses-Ad.sTβRFc or mhTERTAd.sTβRFc. Skeletal tumor growth was monitored weekly by bioluminescence imaging (BLI) and radiography. At the termination time on day 28, hind limb bones were analyzed for tumor burden, synchrotron micro-computed tomography, and osteoclast activation. Intravenous delivery of Ad.sTβRFc and mhTERTAd.sTβRFc induced significant inhibition of tumor growth, reduction of tumor burden, osteoclast activation, and increased animals' survival. Oncolytic adenoviruses were safer than dl309, a wild-type virus. A slight elevation of liver enzyme activity was observed after Ad.sTβRFc administration; this subsided with time. Based on these studies, we believe that Ad.sTβRFc and mhTERTAd.sTβRFc can be developed as a safe and effective approach for the treatment of established bone metastasis.

Indexed as

Acid PhosphataseAdenoviridaeAnimalsBone NeoplasmsBreast NeoplasmsFemaleGenetic TherapyHEK293 CellsHumansInjections, IntravenousIsoenzymesMiceMice, Inbred BALB CMice, NudeOncolytic VirotherapyOncolytic VirusesAcid PhosphataseIsoenzymesProtein Serine-Threonine KinasesReceptors, Transforming Growth Factor betaReceptor, Transforming Growth Factor-beta Type IITartrate-Resistant Acid Phosphatase

Identifiers

PMID21712815
PMCPMC3182349
OpenAlexW2067818659

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.