Evidence map›Paper›PMID 30976832›Full record

ReviewCurrent genetics2019

Histone stress: an unexplored source of chromosomal instability in cancer?

Douglas Maya Miles, Chantal Desdouets, Vincent Géli

Open access · greenAbstract readReview
PubMed Publisher
In one paragraph

Review in Current genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 32% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. 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

3 authors at 2 institutions in 1 country.

Douglas Maya MilesMarseille Cancer Research Centre (CRCM), U1068 Inserm, UMR7258, CNRS, Aix-Marseille Université, Institut Paoli-Calmettes, Equipe labellisée Ligue, Marseille, 13273, France.
Chantal DesdouetsCentre de Recherche des Cordeliers, UMR 1162, Inserm, Université Paris Descartes, 75006, Paris, France.
Vincent GéliMarseille Cancer Research Centre (CRCM), U1068 Inserm, UMR7258, CNRS, Aix-Marseille Université, Institut Paoli-Calmettes, Equipe labellisée Ligue, Marseille, 13273, France. vincent.geli@inserm.fr.ORCID http://orcid.org/0000-0002-4103-7462
Centre National de la Recherche Scientifique · FRInserm · FR

Funding

Ligue Contre le Cancer LNNC-Geli-2018
6 · The paper itself

Abstract

Ploidy is stably maintained in most human somatic cells by a sequential and tight coordination of cell cycle events. Undesired whole genome doublings or duplications are frequent in tumours and have been quite recently described as macro-evolutionary events associated with poor prognosis. In vitro and in vivo studies suggest that polyploidy can favour genome instability, facilitate the formation and progression of tumours, and modify their sensitivity to chemotherapeutic agents. Stress is strongly related to changes in ploidy and whole genome doublings. In this review, we summarize different mechanisms that promote polyploidization, describe a new type of stress able to trigger WGDs in S. cerevisiae, histone stress, and provide some examples and theoretical scenarios that support that cancer cells might suffer from this type of stress. We finally highlight some results showing that the kinase Swe1 (Wee1 in humans) has a role in sensing histone levels before cells enter mitosis, thereby avoiding their undesired consequences on chromosome segregation and ploidy control.

Indexed as

Chromosomal InstabilityStress, PhysiologicalAnimalsCell CycleDisease SusceptibilityGenomic InstabilityHistonesHumansNeoplasmsPolyploidySaccharomyces cerevisiaeHistonesCancerGenome instabilityHistonesPolyploidySwe1Whole genome duplication

Identifiers

PMID30976832
OpenAlexW2936091015

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.