Evidence map›Paper›PMID 24196441›Full record

ArticleCell cycle (Georgetown, Tex.)2014

CtIP is required for DNA damage-dependent induction of P21.

Bo Liu, Rixin Cong, Bin Peng, Bingtao Zhu, Gelin Dou, Haiyan Ai, Xiaodong Zhang, Zhenghe Wang, Xingzhi Xu

Open access · hybridAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 45% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

9 authors at 4 institutions in 2 countries.

Bo LiuBeijing Key laboratory of DNA Damage Response; Capital Normal University; College of Life Sciences; Beijing, China.
Rixin CongBeijing Key laboratory of DNA Damage Response; Capital Normal University; College of Life Sciences; Beijing, China.
Bin PengBeijing Key laboratory of DNA Damage Response; Capital Normal University; College of Life Sciences; Beijing, China.
Bingtao ZhuBeijing Key laboratory of DNA Damage Response; Capital Normal University; College of Life Sciences; Beijing, China.
Gelin DouBeijing Key laboratory of DNA Damage Response; Capital Normal University; College of Life Sciences; Beijing, China.
Haiyan AiBeijing Key laboratory of DNA Damage Response; Capital Normal University; College of Life Sciences; Beijing, China.
Xiaodong ZhangCollege of Life Sciences; Wuhan University; Wuhan, Hubei, China.
Zhenghe WangDepartment of Genetics and Case Comprehensive Cancer Center; Case Western Reserve University; Cleveland, OH USA.
Xingzhi XuBeijing Key laboratory of DNA Damage Response; Capital Normal University; College of Life Sciences; Beijing, China.
Capital Normal University · CNBeijing Normal University · CNCase Western Reserve University · USWuhan Business University · CN

Funding

Development of a universal tagging method for genome wide ChIP analysesR01HG004722 · NHGRI · CASE WESTERN RESERVE UNIVERSITY · PI SCACHERI, PETER CHRISTOPHER, WANG, ZHENGHE · 2008 to 2010
$1.4M
Next-generation mouse gene-targeting technology to model tumorigenesisR21CA181859 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI WANG, ZHENGHE · 2013 to 2015
$682k
Developing novel technology for mapping dynamic oncoprotein interaction networksR21CA160060 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI WANG, ZHENGHE · 2012 to 2013
$464k
NCI NIH HHS R21 CA160060NCI NIH HHS R21 CA181859NHGRI NIH HHS R01 HG004722
6 · The paper itself

Abstract

DNA endonuclease CtIP is involved in both DNA double-strand break (DSB) repair and transcriptional repression/activation. The cyclin-dependent kinase inhibitor P21, which is induced at transcription level in response to a variety of stresses, controls G₁/S transition. In this report, we found that CtIP bound to the P21 promoter, and this binding was enhanced in response to DNA damage. Concomitantly, ectopic expression of CtIP increased P21 promoter activity, and this increment was enhanced upon camptothecin treatment. Conversely, DNA damage failed to induce P21 gene expression in CtIP-deficient cells. Taken together, our data demonstrate that CtIP is required for DNA damage-induced P21 induction.

Indexed as

Carrier ProteinsCyclin-Dependent Kinase Inhibitor p21DNA DamageEndodeoxyribonucleasesG1 Phase Cell Cycle CheckpointsGene Expression Regulation, DevelopmentalHumansMCF-7 CellsNuclear ProteinsPromoter Regions, GeneticCarrier ProteinsCyclin-Dependent Kinase Inhibitor p21EndodeoxyribonucleasesNuclear ProteinsRBBP8 protein, humanDNA damageDNA endonuclease CtIPP21

Identifiers

PMID24196441
PMCPMC3925741
OpenAlexW1997191259

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.