Evidence map›Paper›PMID 22559204›Full record

ArticleRadiation research2012

Spatially fractionated radiation induces cytotoxicity and changes in gene expression in bystander and radiation adjacent murine carcinoma cells.

Rajalakshmi S Asur, Sunil Sharma, Ching-Wei Chang, Jose Penagaricano, Indira M Kommuru, Eduardo G Moros, Peter M Corry, Robert J Griffin

Abstract read
In one paragraph

Article in Radiation research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
4.5field-weighted citation impact, top 6% 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

53 citing papers in PubMed, 90 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Rajalakshmi S AsurDepartment of Radiation Oncology, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205, USA.
Sunil Sharma
Ching-Wei Chang
Jose Penagaricano
Indira M Kommuru
Eduardo G Moros
Peter M Corry
Robert J Griffin
University of Arkansas for Medical Sciences · USMoffitt Cancer Center · US

Funding

PHYSIOLOGICAL FACTORS IN HYPERTHERMIAR01CA044114 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI GRIFFIN, ROBERT JAMES · 1987 to 2012
$3.3M
Study of anti-angiogenesis enhanced radiotherapyR01CA107160 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI GRIFFIN, ROBERT JAMES · 2005 to 2008
$973k
NCI NIH HHS CA44114NCI NIH HHS R01 CA044114NCI NIH HHS R01 CA107160
6 · The paper itself

Abstract

Radiation-induced bystander effects have been extensively studied at low doses, since evidence of bystander induced cell killing and other effects on unirradiated cells were found to be predominant at doses up to 0.5 Gy. Therefore, few studies have examined bystander effects induced by exposure to higher doses of radiation, such as spatially fractionated radiation (GRID) treatment. In the present study, we evaluate the ability of GRID treatment to induce changes in GRID adjacent (bystander) regions, in two different murine carcinoma cell lines following exposure to a single irradiation dose of 10 Gy. Murine SCK mammary carcinoma cells and SCCVII squamous carcinoma cells were irradiated using a brass collimator to create a GRID pattern of nine circular fields 12 mm in diameter with a center-to-center distance of 18 mm. Similar to the typical clinical implementation of GRID, this is approximately a 50:50 ratio of direct and bystander exposure. We also performed experiments by irradiating separate cultures and transferring the medium to unirradiated bystander cultures. Clonogenic survival was evaluated in both cell lines to determine the occurrence of radiation-induced bystander effects. For the purpose of our study, we have defined bystander cells as GRID adjacent cells that received approximately 1 Gy scatter dose or unirradiated cells receiving conditioned medium from irradiated cells. We observed significant bystander killing of cells adjacent to the GRID irradiated regions compared to sham treated controls. We also observed bystander killing of SCK and SCCVII cells cultured in conditioned medium obtained from cells irradiated with 10 Gy. Therefore, our results confirm the occurrence of bystander effects following exposure to a high-dose of radiation and suggest that cell-to-cell contact is not required for these effects. In addition, the gene expression profile for DNA damage and cellular stress response signaling in SCCVII cells after GRID exposure was studied. The occurrence of GRID-induced bystander gene expression changes in significant numbers of DNA damage and cellular stress response signaling genes, providing molecular evidence for possible mechanisms of bystander cell killing.

Indexed as

Dose Fractionation, RadiationAnimalsBystander EffectCarcinoma, Squamous CellCell Line, TumorCell SurvivalDNA DamageDose-Response Relationship, RadiationFilm DosimetryGene Expression Regulation, NeoplasticMammary Neoplasms, ExperimentalMiceOxidative StressSignal Transduction

Identifiers

PMID22559204
PMCPMC3395590
OpenAlexW2033649139

What OpenQuestion holds

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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.