Evidence map›Paper›PMID 25190155›Full record

ArticleJournal of radiation research2015

Dose- and time-dependent gene expression alterations in prostate and colon cancer cells after in vitro exposure to carbon ion and X-irradiation.

Annelies Suetens, Marjan Moreels, Roel Quintens, Els Soors, Jasmine Buset, Sabina Chiriotti, Kevin Tabury, Vincent Gregoire, Sarah Baatout

Open access · goldAbstract read
In one paragraph

Article in Journal of radiation research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. The 20th Gray lecture 2019: health and heavy ions.The British journal of radiology · 2020
    Review
  9. Article
  10. Review
  11. Myosin Heavy Chain 9: Oncogene or Tumor Suppressor Gene?Medical science monitor : international medical journal of experimental and clinical research · 2019
    Review
  12. High LET Radiation OvercomesTechnology in cancer research & treatment · 2019
    Article
  13. Article
  14. Article
  15. 3d Tissue Engineered In Vitro Models Of Cancer In Bone.ACS biomaterials science & engineering · 2018
    Article
  16. Article
  17. Gene Expression Studies for the Development of Particle Therapy.International journal of particle therapy · 2018
    Article
  18. Review
  19. Article
  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

9 authors at 3 institutions in 1 country.

Annelies SuetensRadiobiology Unit, Expert Group for Molecular and Cellular Biology, Institute for Environment, Health and Safety, Belgian Nuclear Research Centre, Boeretang 200, 2400 Mol, Belgium Radiation Oncology Department and Center for Molecular Imaging, Radiotherapy and Oncology, Institut de Recherche Expérimentale et Clinique (IREC), Université Catholique de Louvain (UCL), B1.5407 Avenue Hippocrate, No. 54-55, 1200 Bruxelles, Belgium.
Marjan MoreelsRadiobiology Unit, Expert Group for Molecular and Cellular Biology, Institute for Environment, Health and Safety, Belgian Nuclear Research Centre, Boeretang 200, 2400 Mol, Belgium.
Roel QuintensRadiobiology Unit, Expert Group for Molecular and Cellular Biology, Institute for Environment, Health and Safety, Belgian Nuclear Research Centre, Boeretang 200, 2400 Mol, Belgium.
Els SoorsRadiobiology Unit, Expert Group for Molecular and Cellular Biology, Institute for Environment, Health and Safety, Belgian Nuclear Research Centre, Boeretang 200, 2400 Mol, Belgium.
Jasmine BusetRadiobiology Unit, Expert Group for Molecular and Cellular Biology, Institute for Environment, Health and Safety, Belgian Nuclear Research Centre, Boeretang 200, 2400 Mol, Belgium.
Sabina ChiriottiRadiation Oncology Department and Center for Molecular Imaging, Radiotherapy and Oncology, Institut de Recherche Expérimentale et Clinique (IREC), Université Catholique de Louvain (UCL), B1.5407 Avenue Hippocrate, No. 54-55, 1200 Bruxelles, Belgium Radiation Protection, Dosimetry and Calibration Expert Group, SCK•CEN, Mol, Belgium.
Kevin TaburyRadiobiology Unit, Expert Group for Molecular and Cellular Biology, Institute for Environment, Health and Safety, Belgian Nuclear Research Centre, Boeretang 200, 2400 Mol, Belgium.
Vincent GregoireRadiation Oncology Department and Center for Molecular Imaging, Radiotherapy and Oncology, Institut de Recherche Expérimentale et Clinique (IREC), Université Catholique de Louvain (UCL), B1.5407 Avenue Hippocrate, No. 54-55, 1200 Bruxelles, Belgium.
Sarah BaatoutRadiobiology Unit, Expert Group for Molecular and Cellular Biology, Institute for Environment, Health and Safety, Belgian Nuclear Research Centre, Boeretang 200, 2400 Mol, Belgium Department of Molecular Biotechnology, Ghent University, Coupure links 653, Ghent, Belgium sarah.baatout@sckcen.be.
Belgian Nuclear Research Centre · BEUCLouvain · BEGhent University · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hadrontherapy is an advanced form of radiotherapy that uses beams of charged particles (such as protons and carbon ions). Compared with conventional radiotherapy, the main advantages of carbon ion therapy are the precise absorbed dose localization, along with an increased relative biological effectiveness (RBE). This high ballistic accuracy of particle beams deposits the maximal dose to the tumor, while damage to the surrounding healthy tissue is limited. Currently, hadrontherapy is being used for the treatment of specific types of cancer. Previous in vitro studies have shown that, under certain circumstances, exposure to charged particles may inhibit cell motility and migration. In the present study, we investigated the expression of four motility-related genes in prostate (PC3) and colon (Caco-2) cancer cell lines after exposure to different radiation types. Cells were irradiated with various absorbed doses (0, 0.5 and 2 Gy) of accelerated (13)C-ions at the GANIL facility (Caen, France) or with X-rays. Clonogenic assays were performed to determine the RBE. RT-qPCR analysis showed dose- and time-dependent changes in the expression of CCDC88A, FN1, MYH9 and ROCK1 in both cell lines. However, whereas in PC3 cells the response to carbon ion irradiation was enhanced compared with X-irradiation, the effect was the opposite in Caco-2 cells, indicating cell-type-specific responses to the different radiation types.

Indexed as

Heavy IonsCaco-2 CellsCarbonCarbon IsotopesCell Line, TumorColonic NeoplasmsDose-Response Relationship, RadiationGene Expression Regulation, NeoplasticHumansMaleNeoplasm ProteinsProstatic NeoplasmsRadiation DosageX-RaysCarbonCarbon IsotopesNeoplasm ProteinsCaco-2 colon adenocarcinomacarbon ion irradiationcolony survival assaygene expressionmotility genesPC3 prostate adenocarcinoma

Identifiers

PMID25190155
PMCPMC4572596
OpenAlexW2165345566

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.