Evidence map›Paper›PMID 24377047›Full record

ArticleRadiology research and practice2013

Whole body microwave irradiation for improved dacarbazine therapeutical action in cutaneous melanoma mouse model.

Monica Neagu, Carolina Constantin, Diana Martin, Lucian Albulescu, Nicusor Iacob, Daniel Ighigeanu

Abstract read
In one paragraph

Article in Radiology research and practice, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. 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

6 authors.

Monica NeaguImmunology Department, Immunobiology Laboratory, "Victor Babes" National Institute of Pathology, 99-101 Splaiul Independentei, sector 5, Bucharest 050096, Romania.
Carolina ConstantinImmunology Department, Immunobiology Laboratory, "Victor Babes" National Institute of Pathology, 99-101 Splaiul Independentei, sector 5, Bucharest 050096, Romania.
Diana MartinNational Institute for Laser, Plasma and Radiation Physics, 409 Atomistilor Street, Magurele 077125, Romania.
Lucian AlbulescuDepartment of Infectious Diseases and Immunology, Virology Division, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 1, 3584 CL Utrecht, The Netherlands.
Nicusor IacobNational Institute for Laser, Plasma and Radiation Physics, 409 Atomistilor Street, Magurele 077125, Romania.
Daniel IghigeanuNational Institute for Laser, Plasma and Radiation Physics, 409 Atomistilor Street, Magurele 077125, Romania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A cutaneous melanoma mouse model was used to test the efficacy of a new therapeutical approach that uses low doses of cytostatics in conjunction with mild whole body microwave exposure of 2.45 GHz in order to enhance cytostatics antitumoral effect. Materials and Methods. A microwave exposure system for C57BL/6 mouse whole body microwave irradiation was designed; groups of 40 mice (males and females) bearing experimental tumours were subjected to a combined therapy comprising low doses of dacarbazine in combination with mild whole body irradiation. Clinical parameters and serum cytokine testing using xMAP technology were performed. Results. The group that was subjected to combined therapy, microwave and cytostatic, had the best clinical evolution in terms of overall survival, tumour volume, and metastatic potential. At day 14 the untreated group had 100% mortality, while in the combined therapy group 40% of mice were surviving. Quantifying serum IL-1 β , IL-6, IL-10, IL-12 (p70), IFN- γ , GM-CSF, TNF- α , MIP-1 α , MCP-1, and KC during tumorigenesis and therapy found that the combined experimental therapy decreases all the inflammatory cytokines, except chemokine MCP-1 that was found increased, suggesting an increase of the anti-tumoral immune response triggered by the combined therapy. The overall metastatic process is decreased in the combined therapy group.

Identifiers

PMID24377047
PMCPMC3860147

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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.