Evidence map›Paper›PMID 17851138›Full record

ReviewDNA repair2008

Turning off the G2 DNA damage checkpoint.

Teresa M Calonge, Matthew J O'Connell

Open access · greenAbstract readReview
In one paragraph

Review in DNA repair, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

18 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. DNA damage checkpoint execution and the rules of its disengagement.Frontiers in cell and developmental biology · 2022
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Regulatory motifs in Chk1.Cell cycle (Georgetown, Tex.) · 2013
    Article
  11. CCT244747 is a novel potent and selective CHK1 inhibitor with oral efficacy alone and in combination with genotoxic anticancer drugs.Clinical cancer research : an official journal of the American Association for Cancer Research · 2012
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Regulation of chk1.Cell division · 2009
    Article
  17. Regulation of Chk1 by its C-terminal domain.Molecular biology of the cell · 2008
    Article
  18. 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

2 authors at 1 institution in 1 country.

Teresa M CalongeDepartment of Oncological Sciences, Mount Sinai School of Medicine, New York, NY 10029, USA.
Matthew J O'Connell
Icahn School of Medicine at Mount Sinai · US

Funding

Chk1 signaling in the G2 DNA damage checkpointR01CA100076 · NCI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI O'CONNELL, MATTHEW J · 2003 to 2007
$1.7M
Chk1 signaling in the G2 DNA damage checkpointR56CA100076 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI O'CONNELL, MATTHEW J · 2009 to 2009
$336k
NCI NIH HHS CA 100076NCI NIH HHS R01 CA100076NCI NIH HHS R56 CA100076
6 · The paper itself

Abstract

In response to DNA damage, cells activate checkpoints to delay cell cycle progression and allow time for completion of DNA repair before commitment to S-phase or mitosis. During G2, many proteins collaborate to activate Chk1, an effector protein kinase that ensures the mitotic cyclin-dependent kinase remains in an inactive state. This checkpoint is ancient in origin and highly conserved from fission yeast to humans. Work from many groups has led to a detailed description of the spatiotemporal control of signaling events leading to Chk1 activation. However, to survive DNA damage in G2, the checkpoint must be inactivated to allow resumption of cell cycling and entry into mitosis. Though only beginning to be understood, here we review current data regarding checkpoint termination signals acting on Chk1 and its' upstream regulators.

Indexed as

Checkpoint Kinase 1DNA DamageG2 PhaseGene Expression RegulationGenes, cdcPhosphorylationProtein KinasesCheckpoint Kinase 1CHEK1 protein, humanProtein Kinases

Identifiers

PMID17851138
PMCPMC2233850
OpenAlexW2170787272

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.