Evidence map›Paper›PMID 33590416›Full record

ArticleMolecular biology reports2021

Profilin-1; a novel regulator of DNA damage response and repair machinery in keratinocytes.

Chang-Jin Lee, Min-Ji Yoon, Dong Hyun Kim, Tae Uk Kim, Youn-Jung Kang

Open access · hybridAbstract read
In one paragraph

Article in Molecular biology reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 35% 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, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
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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

5 authors at 2 institutions in 1 country.

Chang-Jin Lee *Department of Biomedical Science, School of Life Science, CHA University, Seongnam-si, Gyunggi-do, South Korea.
Min-Ji Yoon *Department of Biomedical Science, School of Life Science, CHA University, Seongnam-si, Gyunggi-do, South Korea.
Dong Hyun KimDepartment of Dermatology, CHA Bundang Medical Center, CHA University, Seongnam-si, Gyunggi-do, South Korea.
Tae Uk KimDepartment of Biochemistry, School of Medicine, CHA University, Seongnam-si, Gyunggi-do, South Korea.
Youn-Jung KangDepartment of Biomedical Science, School of Life Science, CHA University, Seongnam-si, Gyunggi-do, South Korea. yjkang@cha.ac.kr.ORCID http://orcid.org/0000-0002-0771-9515
CHA University · KRCHA University Bundang Medical Center · KR

Funding

Ministry of Health and Welfare HI16C1559National Research Foundation of Korea 2018R1C1B6003
6 · The paper itself

Abstract

Profilin-1 (PFN1) regulates actin polymerization and cytoskeletal growth. Despite the essential roles of PFN1 in cell integration, its subcellular function in keratinocyte has not been elucidated yet. Here we characterize the specific regulation of PFN1 in DNA damage response and repair machinery. PFN1 depletion accelerated DNA damage-mediated apoptosis exhibiting PTEN loss of function instigated by increased phosphorylated inactivation followed by high levels of AKT activation. PFN1 changed its predominant cytoplasmic localization to the nucleus upon DNA damage and subsequently restored the cytoplasmic compartment during the recovery time. Even though γH2AX was recruited at the sites of DNA double strand breaks in response to DNA damage, PFN1-deficient cells failed to recruit DNA repair factors, whereas control cells exhibited significant increases of these genes. Additionally, PFN1 depletion resulted in disruption of PTEN-AKT cascade upon DNA damage and CHK1-mediated cell cycle arrest was not recovered even after the recovery time exhibiting γH2AX accumulation. This might suggest PFN1 roles in regulating DNA damage response and repair machinery to protect cells from DNA damage. Future studies addressing the crosstalk and regulation of PTEN-related DNA damage sensing and repair pathway choice by PFN1 may further aid to identify new mechanistic insights for various DNA repair disorders.

Indexed as

ActinsApoptosisCell Cycle CheckpointsCheckpoint Kinase 1CytoplasmCytoskeletonDNA DamageDNA RepairDNA Repair-Deficiency DisordersHistonesHumansKeratinocytesPhosphorylationProfilinsActinsCheckpoint Kinase 1CHEK1 protein, humanH2AX protein, humanHistonesPFN1 protein, humanProfilinsCell integrationDNA damage responseDNA repairKeratinocyteProfilin-1

Identifiers

PMID33590416
PMCPMC7925496
OpenAlexW3133373408

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.