Evidence map›Paper›PMID 25244922›Full record

ReviewMolecular cancer research : MCR2015

Telomere-regulating genes and the telomere interactome in familial cancers.

Carla Daniela Robles-Espinoza, Martin del Castillo Velasco-Herrera, Nicholas K Hayward, David J Adams

Open access · greenAbstract readReview
In one paragraph

Review in Molecular cancer research : MCR, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 2 pooled it
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

24 citing papers in PubMed, 2 syntheses or guidelines pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. Article
  6. Cutaneous melanoma.Nature reviews. Disease primers · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Biomedicines · 2021
    Article
  12. Review
  13. Article
  14. TheCells · 2020
    Review
  15. Review
  16. Review
  17. Genetic variants inJournal of Cancer · 2019
    Article
  18. Review
  19. Review
  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

4 authors at 2 institutions in 2 countries.

Carla Daniela Robles-EspinozaExperimental Cancer Genetics, Wellcome Trust Sanger Institute, Hinxton, United Kingdom. cdre@sanger.ac.uk.
Martin del Castillo Velasco-HerreraExperimental Cancer Genetics, Wellcome Trust Sanger Institute, Hinxton, United Kingdom.
Nicholas K HaywardOncogenomics Laboratory, QIMR Berghofer Medical Research Institute, Herston, Brisbane, Queensland, Australia.
David J AdamsExperimental Cancer Genetics, Wellcome Trust Sanger Institute, Hinxton, United Kingdom.
Wellcome Sanger Institute · GBQIMR Berghofer Medical Research Institute · AU

Funding

Cancer Research UK 13031Cancer Research UK A12401Cancer Research UK A13031Cancer Research UK A14356Wellcome TrustWellcome Trust WT098051
6 · The paper itself

Abstract

Telomeres are repetitive sequence structures at the ends of linear chromosomes that consist of double-stranded DNA repeats followed by a short single-stranded DNA protrusion. Telomeres need to be replicated in each cell cycle and protected from DNA-processing enzymes, tasks that cells execute using specialized protein complexes such as telomerase (that includes TERT), which aids in telomere maintenance and replication, and the shelterin complex, which protects chromosome ends. These complexes are also able to interact with a variety of other proteins, referred to as the telomere interactome, to fulfill their biological functions and control signaling cascades originating from telomeres. Given their essential role in genomic maintenance and cell-cycle control, germline mutations in telomere-regulating proteins and their interacting partners have been found to underlie a variety of diseases and cancer-predisposition syndromes. These syndromes can be characterized by progressively shortening telomeres, in which carriers can present with organ failure due to stem cell senescence among other characteristics, or can also present with long or unprotected telomeres, providing an alternative route for cancer formation. This review summarizes the critical roles that telomere-regulating proteins play in cell-cycle control and cell fate and explores the current knowledge on different cancer-predisposing conditions that have been linked to germline defects in these proteins and their interacting partners.

Indexed as

Cell Cycle ProteinsGenetic Predisposition to DiseaseGerm-Line MutationHumansNeoplasmsTelomereTelomere-Binding ProteinsTelomere ShorteningCell Cycle ProteinsTelomere-Binding Proteins

Identifiers

PMID25244922
PMCPMC4278843
OpenAlexW2100838748

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.