Evidence map›Paper›PMID 24858045›Full record

ReviewOncogene2015

Less understood issues: p21(Cip1) in mitosis and its therapeutic potential.

N-N Kreis, F Louwen, J Yuan

Abstract readReview
PubMed Publisher
In one paragraph

Review in Oncogene, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

73 citing papers in PubMed, 114 citations in OpenAlex.

  1. Article
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  6. ALYREF-mediated mInternational journal of biological sciences · 2026
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13 more citing papers are in PubMed but not listed here.

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.

N-N KreisDepartment of Gynecology and Obstetrics, J.W. Goethe-University, Frankfurt, Germany.
F LouwenDepartment of Gynecology and Obstetrics, J.W. Goethe-University, Frankfurt, Germany.
J YuanDepartment of Gynecology and Obstetrics, J.W. Goethe-University, Frankfurt, Germany.
Goethe University Frankfurt · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

p21(Cip1) is a multifunctional protein and a key player in regulating different cellular processes. The transcription of p21 is regulated by p53-dependent and -independent pathways. The expression of p21 is increased in response to various cellular stresses to arrest the cell cycle and ensure genomic stability. p21 has been shown to be a tumor suppressor and an oncogene as well. The function of p21 in mitosis has been proposed but not systematically studied. We have recently shown that p21 binds to and inhibits the activity of Cdk1/cyclin B1, and is important for a fine-tuned mitotic progression. Loss of p21 prolongs the duration of mitosis and results in severe mitotic defects like chromosome segregation and cytokinesis failures promoting consequently genomic instability. Moreover, p21 is dramatically stabilized in mitotic tumor cells upon treatment with mitotic agents like paclitaxel or mitotic kinase inhibitors. Increased p21 is mainly localized in the cytoplasm and associates with cell survival indicating a crucial role of p21 in susceptibility to mitotic agents in tumor cells. In this review we will briefly summarize the structure and general physiological functions as well as regulation of p21, discuss in detail its role in mitosis and its potential to serve as a therapeutic target.

Indexed as

CDC2 Protein KinaseCell Cycle CheckpointsCell SurvivalChromosome SegregationCyclin B1Cyclin-Dependent Kinase Inhibitor p21Cyclin-Dependent KinasesCytokinesisGenomic InstabilityHumansMicrotubule-Associated ProteinsMitosisPaclitaxelPhosphorylationTubulin ModulatorsTumor Suppressor Protein p53CCNB1 protein, humanCDC2 Protein KinaseCDK1 protein, humanCDKN1A protein, humanCyclin B1Cyclin-Dependent Kinase Inhibitor p21Cyclin-Dependent KinasesKIF23 protein, humanMicrotubule-Associated ProteinsPaclitaxelTP53 protein, humanTubulin ModulatorsTumor Suppressor Protein p53

Identifiers

PMID24858045
OpenAlexW2095195934

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.