Evidence map›Paper›PMID 23065374›Full record

ArticleMolecular neurobiology2013

Telomere profiling: toward glioblastoma personalized medicine.

Sylvain Ferrandon, Paul Saultier, Julien Carras, Priscillia Battiston-Montagne, Gersende Alphonse, Michael Beuve, Céline Malleval, Jérôme Honnorat, Tania Slatter, Noelyn Hung and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular neurobiology, 2013. 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
2.0field-weighted citation impact, top 13% 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, 33 citations in OpenAlex.

  1. Pooled it
  2. Telomere length and risk of glioma.Cancer epidemiology · 2013
    Trial
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Non-canonical roles of canonical telomere binding proteins in cancers.Cellular and molecular life sciences : CMLS · 2021
    Review
  9. Article
  10. Review
  11. Review
  12. CoA Synthase (Cancer research · 2020
    Article
  13. POT1-TPP1 telomere length regulation and disease.Computational and structural biotechnology journal · 2020
    Review
  14. Hadrontherapy Interactions in Molecular and Cellular Biology.International journal of molecular sciences · 2019
    Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. The effect of LOXL2 in hepatocellular carcinoma.Molecular medicine reports · 2016
    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

13 authors at 5 institutions in 2 countries.

Sylvain FerrandonEMR3738, Cellular and Molecular Radiobiology Laboratory, Medicine Faculty, Lyon 1 University, 69921, Oullins Cedex 12, France.
Paul Saultier
Julien Carras
Priscillia Battiston-Montagne
Gersende Alphonse
Michael Beuve
Céline Malleval
Jérôme Honnorat
Tania Slatter
Noelyn Hung
Janice Royds
Claire Rodriguez-Lafrasse
Delphine Poncet
Université Claude Bernard Lyon 1 · FRHospices Civils de Lyon · FRUniversity of Otago · NZInserm · FRInstitute of Nuclear Physics of Lyon · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite a standard of care combining surgery, radiotherapy (RT), and temozolomide chemotherapy, the average overall survival (OS) of glioblastoma patients is only 15 months, and even far lower when the patient cannot benefit from this combination. Therefore, there is a strong need for new treatments, such as new irradiation techniques. Against this background, carbon ion hadrontherapy, a new kind of irradiation, leads to a greater biological response of the tumor, while minimizing adverse effects on healthy tissues in comparison with RT. As carbon ion hadrontherapy is restricted to RT-resistant patients, photon irradiation resistance biomarkers are needed. Long telomeres and high telomerase activity have been widely associated with photon radioresistance in other cancers. Moreover, telomere protection, telomere function, and telomere length (TL) also depend on the shelterin protein complex (TRF1, TRF2, TPP1, POT1, TIN2, and hRAP1). We thus decided to evaluate an enlarged telomeric status (TL, telomerase catalytic subunit, and the shelterin component expression level) as a potential radioresistance biomarker in vitro using cellular models and ex vivo using patient tumor biopsies. In addition, nothing was known about the role of telomeres in carbon ion response. We thus evaluated telomeric status after both types of irradiation. We report here a significant correlation between TL and the basal POT1 expression level and photon radioresistance, in vitro, and a significant increase in the OS of patients with long telomeres or a high POT1 level, in vivo. POT1 expression was predictive of patient response irrespective of the TL. Strikingly, these correlations were lost, in vitro, when considering carbon irradiation. We thus propose (1) a model of the implications of telomeric damage in the cell response to both types of irradiation and (2) assessment of the POT1 expression level and TL using patient tumor biopsies to identify radioresistant patients who could benefit from carbon hadrontherapy.

Indexed as

Precision MedicineBrain NeoplasmsCell Line, TumorGlioblastomaHeavy Ion RadiotherapyHumansPhotonsRadiation ToleranceShelterin ComplexSurvival AnalysisTelomeraseTelomereTelomere-Binding ProteinsACD protein, humanShelterin ComplexTelomeraseTelomere-Binding ProteinsTERT protein, human

Identifiers

PMID23065374
OpenAlexW2094566075

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.