Evidence map›Paper›PMID 15905856›Full record

ArticleCancer gene therapy2005

Inhibition of angiogenesis and HGF-cMET-elicited malignant processes in human hepatocellular carcinoma cells using adenoviral vector-mediated NK4 gene therapy.

Daniëlle A M Heideman, Renée M Overmeer, Victor W van Beusechem, Wouter H Lamers, Theodorus B M Hakvoort, Peter J F Snijders, Mikael E Craanen, G Johan A Offerhaus, Chris J L M Meijer, Winald R Gerritsen

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In one paragraph

Article in Cancer gene therapy, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 32 citations in OpenAlex.

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  11. Liver regeneration and tumor stimulation--a review of cytokine and angiogenic factors.Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract · 2008
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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

10 authors at 2 institutions in 1 country.

Daniëlle A M HeidemanDepartment of Pathology, VU University Medical Center, PO Box 7057, 1007 MB Amsterdam, The Netherlands. dam.heideman@vumc.nl
Renée M Overmeer
Victor W van Beusechem
Wouter H Lamers
Theodorus B M Hakvoort
Peter J F Snijders
Mikael E Craanen
G Johan A Offerhaus
Chris J L M Meijer
Winald R Gerritsen
Amsterdam UMC Location VUmc · NLAcademic Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

NK4 is an hepatocyte growth factor (HGF)-antagonist and a broad angiogenesis inhibitor. NK4 gene therapy has confirmed antitumor efficacy on cancers with intact HGF-cMET signaling pathway. However, the feasibility to treat tumors in which the effect of the HGF-cMET signaling pathway is less unambiguous or may even be inhibitory on carcinogenesis, such as hepatocellular carcinoma (HCC) with NK4 needs further assessment. Therefore, we evaluated the effects of adenoviral vector-mediated expression of NK4 on the biological behavior of a series of HCC cell lines in vitro and on HepG2 xenografts in vivo. In vitro, transduction of HCC cell lines with the replication-deficient recombinant adenoviral vector AdCMV.NK4 resulted in significant inhibition of proliferation over and above the antimitogenic effects of HGF. In addition, HGF-induced scattering and invasion through matrigel were inhibited effectively. Moreover, transduced HCC cells produced sufficient amounts of NK4 protein to achieve bystander effects involving reduced migration of nontransduced tumor cells and reduced proliferation of endothelial cells. Finally, treatment of established HepG2 xenografts with AdCMV.NK4 resulted in significant tumor growth delay and significant reduction of intratumoral microvessel density. In conclusion, NK4 gene therapy is a promising strategy to treat HCC based on the pleiotropic functions of NK4 interfering with tumor growth, invasion, metastasis and angiogenesis.

Indexed as

Genetic TherapyAdenoviridaeAnimalsCarcinoma, HepatocellularCell MovementCell ProliferationCells, CulturedEndothelial CellsGenetic VectorsGene Transfer TechniquesHepatocyte Growth FactorHumansMiceMice, NudeProto-Oncogene Proteins c-metXenograft Model Antitumor AssaysHepatocyte Growth FactorHGF protein, humanProto-Oncogene Proteins c-met

Identifiers

PMID15905856
OpenAlexW2170370631

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.