Evidence map›Paper›PMID 18706976›Full record

ReviewBiochimica et biophysica acta2008

Studying chromosome instability in the mouse.

Floris Foijer, Viji M Draviam, Peter K Sorger

Open access · greenAbstract readReview
In one paragraph

Review in Biochimica et biophysica acta, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

35 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Principles and dynamics of spindle assembly checkpoint signalling.Nature reviews. Molecular cell biology · 2023
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Aneuploidy in stem cells.World journal of stem cells · 2016
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Chromosome instability induced by Mps1 and p53 mutation generates aggressive lymphomas exhibiting aneuploidy-induced stress.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  19. Review
  20. Spindle checkpoint deficiency is tolerated by murine epidermal cells but not hair follicle stem cells.Proceedings of the National Academy of Sciences of the United States of America · 2013
    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 1 institution in 1 country.

Floris FoijerHarvard Medical School, Department of Systems Biology, 200 Longwood Avenue, Boston, MA 02115, USA.
Viji M Draviam
Peter K Sorger
Harvard University · US

Funding

BIOCHEMICAL AND GENETIC ANALYSIS OF YEAST KINETOCHORESR01GM051464 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SORGER, PETER KARL · 1994 to 2010
$3.9M
CELL AND TUMOR GENETICS OF MITOTIC ARREST CHECKPOINTSR01CA084179 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SORGER, PETER KARL · 2000 to 2010
$3.5M
NCI NIH HHS CA84179NCI NIH HHS R01 CA084179NIGMS NIH HHS GM51464NIGMS NIH HHS R01 GM051464
6 · The paper itself

Abstract

Aneuploidy has long been recognized as one of the hallmarks of cancer. It nonetheless remains uncertain whether aneuploidy occurring early in the development of a cancer is a primary cause of oncogenic transformation, or whether it is an epiphenomenon that arises from a general breakdown in cell cycle control late in tumorigenesis. The accuracy of chromosome segregation is ensured both by the intrinsic mechanics of mitosis and by an error-checking spindle assembly checkpoint. Many cancers show altered expression of proteins involved in the spindle checkpoint or in proteins implicated in other mitotic processes. To understand the role of aneuploidy in the initiation and progression of cancer, a number of spindle checkpoint genes have been disrupted in mice, most through conventional gene targeting (to create germ-line knockouts). We describe the consequence of these mutations with respect to embryonic development, tumor progression and an unexpected link to premature aging; readers are referred elsewhere [1] for a discussion of other cell cycle regulators.

Indexed as

AneuploidyAnimalsAutoantigensCell Cycle ProteinsCentromere Protein ACentromere Protein BCentrosomeChromosomal InstabilityChromosomal Proteins, Non-HistoneChromosome SegregationGene DeletionGenes, Tumor SuppressorHumansKinetochoresMad2 ProteinsMiceAutoantigensCell Cycle ProteinsCentromere Protein ACentromere Protein BChromosomal Proteins, Non-HistoneMad2l2 protein, mouseMad2 ProteinsNuclear Proteins

Identifiers

PMID18706976
PMCPMC2923435
OpenAlexW2154428950

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.