Evidence map›Paper›PMID 26383678›Full record

ReviewInternational journal of radiation oncology, biology, physics2015

BRCA1 Mutation: A Predictive Marker for Radiation Therapy?

Charlene Kan, Junran Zhang

Abstract readReview
In one paragraph

Review in International journal of radiation oncology, biology, physics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

29 citing papers in PubMed, 54 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. International journal of molecular sciences · 2023
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Outcomes After Breast Radiation Therapy in a Diverse Patient Cohort With a Germline BRCA1/2 Mutation.International journal of radiation oncology, biology, physics · 2022
    Article
  16. Prevalence of Clinically Relevant GermlineFrontiers in genetics · 2022
    Article
  17. Article
  18. Preclinical evaluation of radiation therapy ofInternational journal of biological sciences · 2021
    Article
  19. Review
  20. 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

2 authors at 1 institution in 1 country.

Charlene KanDepartment of Radiation Oncology, Case Western Reserve University School of Medicine, Cleveland, Ohio.
Junran ZhangDepartment of Radiation Oncology, Case Western Reserve University School of Medicine, Cleveland, Ohio. Electronic address: Junran.zhang@case.edu.
University School · US

Funding

THE ROLE OF NEDD4-1 IN IGF-1R SIGNALINGR01CA154625 · NCI · WASHINGTON UNIVERSITY · PI ZHANG, JUNRAN · 2011 to 2016
$1.6M
NCI NIH HHS R01 CA154625NCI NIH HHS R01CA154625
6 · The paper itself

Abstract

DNA repair, in particular, DNA double-strand break (DSB) repair, is essential for the survival of both normal and cancer cells. An elaborate repair mechanism has been developed in cells to efficiently repair the damaged DNA. The pathways predominately involved in DSB repair are homologous recombination and classic nonhomologous end-joining, although the alternative NHEJ pathway, a third DSB repair pathway, could also be important in certain contexts. The protein of BRCA1 encoded by the tumor suppressor gene BRCA1 regulates all DSB repair pathways. Given that DSBs represent the most biologically significant lesions induced by ionizing radiation and that impaired DSB repair leads to radiation sensitivity, it has been expected that cancer patients with BRCA1 mutations should benefit from radiation therapy. However, the clinical data have been conflicting and inconclusive. We provide an overview about the current status of the data regarding BRCA1 deficiency and radiation therapy sensitivity in both experimental models and clinical investigations. In addition, we discuss a strategy to potentiate the effects of radiation therapy by poly(ADP-ribose) polymerase inhibitors, the pharmacologic drugs being investigated as monotherapy for the treatment of patients with BRCA1/2 mutations.

Indexed as

DNA Breaks, Double-StrandedGenes, BRCA1MutationAnimalsBRCA1 ProteinBreast NeoplasmsDNA DamageDNA End-Joining RepairDNA RepairFemaleGenes, BRCA2Genetic MarkersHumansPoly(ADP-ribose) Polymerase InhibitorsRadiation ToleranceBRCA1 ProteinGenetic MarkersPoly(ADP-ribose) Polymerase Inhibitors

Identifiers

PMID26383678
PMCPMC4576355
OpenAlexW1755658704

What OpenQuestion holds

Textmetadata
LicenceTDM
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.