Evidence map›Paper›PMID 15785954›Full record

ArticleEuropean journal of nuclear medicine and molecular imaging2005

Correlation between 99mTc-(V)-DMSA uptake and constitutive level of phosphorylated focal adhesion kinase in an in vitro model of cancer cell lines.

Delphine Denoyer, Nathalie Perek, Nathalie Le Jeune, Jérôme Cornillon, Francis Dubois

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Article in European journal of nuclear medicine and molecular imaging, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 30 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Delphine DenoyerDepartment of Biophysics and Radiopharmaceuticals, Cell Survival and Adhesion Research Group, Jacques Lisfranc Faculty of Medicine, University of Saint-Etienne, 5 rue Ambroise Paré, 42023, Saint-Etienne, France. delphine.denoyer@univ-st-etienne.fr
Nathalie Perek
Nathalie Le Jeune
Jérôme Cornillon
Francis Dubois
École Nationale d'Ingénieurs de Saint-Étienne · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAlthough a number of prognostic indicators have been developed, it is still difficult to predict the biological behaviour of all cancer types.( 99m)Tc-(V)-DMSA (V DMSA) uptake and focal adhesion kinase (FAK) expression and activation level could be potential agents for this purpose. We hypothesised the existence of a correlation between V DMSA, whose uptake is linked to phosphate ions, essential compounds for tumour growth and cell proliferation, and the adhesion protein FAK, whose elevated expression and level of constitutive activation are implicated in cancer progression. The aim of this study was to assess the relationship between V DMSA incorporation rate and FAK expression and activation by phosphorylation on tyrosine 397 residue.

methodsWe determined V DMSA uptake in six different cancer cell lines and we measured FAK expression and activation by using Western Blotting analysis. Correlations with factors known to be associated with poor prognosis, such as invasive potential, resistance to chemotherapy and proliferation rate, were also investigated.

resultsThe cell lines exhibited different V DMSA incorporation rates. In addition, these cells showed the same FAK expression, but various degrees of activation. A correlation was observed between V DMSA uptake and level of FAK phosphorylation and between V DMSA or constitutive FAK activation and proliferation rate. However, no correlation was shown between these parameters and the other factors tested, i.e. invasive potential and anticancer drug resistance.

conclusionThe results of this in vitro study clearly demonstrate that phosphorylation of FAK, proliferation rate and V DMSA uptake are closely related. Because proliferation and a high level of constitutive FAK activation are linked to cancer progression, it can be assumed that in vivo V DMSA uptake reflects tumour aggressiveness.

Indexed as

RadiopharmaceuticalsTechnetium Tc 99m Dimercaptosuccinic AcidAntineoplastic AgentsBlotting, WesternCell Line, TumorCell ProliferationFocal Adhesion Protein-Tyrosine KinasesHumansIn Vitro TechniquesIonsKineticsNeoplasm InvasivenessNeoplasm MetastasisPhosphatesPhosphorylationPrognosisAntineoplastic AgentsFocal Adhesion Protein-Tyrosine KinasesIonsPhosphatesRadiopharmaceuticalsTechnetium Tc 99m Dimercaptosuccinic AcidTyrosine

Identifiers

PMID15785954
OpenAlexW2065702593

What OpenQuestion holds

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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.