Evidence map›Paper›PMID 27163456›Full record

ArticleCell cycle (Georgetown, Tex.)2016

Negative control of CSL gene transcription by stress/DNA damage response and p53.

Elena Menietti, Xiaoying Xu, Paola Ostano, Jean-Marc Joseph, Karine Lefort, G Paolo Dotto

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

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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

6 authors at 4 institutions in 3 countries.

Elena Meniettia Department of Biochemistry , University of Lausanne , Epalinges , Switzerland.
Xiaoying Xua Department of Biochemistry , University of Lausanne , Epalinges , Switzerland.
Paola Ostanob Cancer Genomics Laboratory, Edo and Elvo Tempia Valenta Foundation , Biella , Italy.
Jean-Marc Josephc Pediatric surgery Department , University Hospital CHUV , Lausanne , Switzerland.
Karine Leforta Department of Biochemistry , University of Lausanne , Epalinges , Switzerland.
G Paolo Dottoa Department of Biochemistry , University of Lausanne , Epalinges , Switzerland.
University Hospital of Lausanne · CHUniversity of Lausanne · CHFondazione Edo ed Elvo Tempia · ITMassachusetts General Hospital · US

Funding

GROWTH DIFFERENTIATION CONTROL IN PRIMARY KERATINOCYTES.R01AR039190 · NIAMS · YALE UNIVERSITY · PI DOTTO, GIAN-PAOLO · 1988 to 2021
$9.5M
Dermal fibroblast/ATF3 control of skin homeostasisR01AR064786 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI DOTTO, GIAN-PAOLO · 2014 to 2018
$1.9M
NIAMS NIH HHS R01 AR039190NIAMS NIH HHS R01 AR064786
6 · The paper itself

Abstract

CSL is a key transcriptional repressor and mediator of Notch signaling. Despite wide interest in CSL, mechanisms responsible for its own regulation are little studied. CSL down-modulation in human dermal fibroblasts (HDFs) leads to conversion into cancer associated fibroblasts (CAF), promoting keratinocyte tumors. We show here that CSL transcript levels differ among HDF strains from different individuals, with negative correlation with genes involved in DNA damage/repair. CSL expression is negatively regulated by stress/DNA damage caused by UVA, Reactive Oxygen Species (ROS), smoke extract, and doxorubicin treatment. P53, a key effector of the DNA damage response, negatively controls CSL gene transcription, through suppression of CSL promoter activity and, indirectly, by increased p21 expression. CSL was previously shown to bind p53 suppressing its activity. The present findings indicate that p53, in turn, decreases CSL expression, which can serve to enhance p53 activity in acute DNA damage response of cells.

Indexed as

Transcription, GeneticCell LineDermisDNA DamageFibroblastsHumansImmunoglobulin J Recombination Signal Sequence-Binding ProteinMaleMutagensOxidative StressReceptors, NotchSignal TransductionTumor Suppressor Protein p53Immunoglobulin J Recombination Signal Sequence-Binding ProteinMutagensRBPJ protein, humanReceptors, NotchTumor Suppressor Protein p53CSL/RBPJκdermal fibroblastsindividual variations in gene transcriptionp53UVA/DNA damage response

Identifiers

PMID27163456
PMCPMC4957600
OpenAlexW2411918998

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.