Evidence map›Paper›PMID 33371766›Full record

ArticleAdipocyte2021

SENP1 is required for the growth, migration, and survival of human adipose-derived stem cells.

Yingying Wu, Beixin Yu, Min Wang

Open access · goldAbstract read
In one paragraph

Article in Adipocyte, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Protein sumoylation in normal and cancer stem cells.Frontiers in molecular biosciences · 2022
    Review
  5. 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

3 authors at 1 institution in 1 country.

Yingying WuCenter for Translational Medicine, The First Affiliated Hospital, Sun Yat-sen University , Guangzhou, China.ORCID 0000-0002-5289-833X
Beixin YuCenter for Translational Medicine, The First Affiliated Hospital, Sun Yat-sen University , Guangzhou, China.
Min WangCenter for Translational Medicine, The First Affiliated Hospital, Sun Yat-sen University , Guangzhou, China.ORCID 0000-0002-2479-6096
Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human adipose-derived stem cells (hADSCs) are adult mesenchymal cells that have attracted the interest of clinical scientists and surgeons due to their large number of advantages including ease of access and expansion, abundance in cell culture, high proliferative rates, and lower senescence. SUMO/sentrin specific protease 1 (SENP1) is a critical protease that is required during the process of SUMOylation and deSUMOylation, which are dynamic mechanisms that influence cell cycle progression, cell proliferation, and apoptotic status. However, the contribution of SENP1 to these important cellular processes in hADSCs is largely uncharacterized and further studies in this area are required. Here, we show for the first time that after knock out SENP1 in hADSCs, their capacity to migrate and proliferate were inhibited, while apoptosis was enhanced. However, SENP1 did not significantly influence the morphology and MSC-related phenotypes of the hADSCs. These results highlight a role for SENP1 during hADSC growth, and its potential as a therapeutic target to improve the efficacy and safety of hADSCs in the clinic.

Indexed as

AdipocytesAdipose TissueApoptosisCell Line, TumorCell MovementCell ProliferationChinaCysteine EndopeptidasesFemaleHumansMaleMesenchymal Stem CellsPeptide HydrolasesSignal TransductionSumoylationCysteine EndopeptidasesPeptide HydrolasesSENP1 protein, humanapoptosisHuman adipose-derived stem cellsmigrationproliferationSENP1

Identifiers

PMID33371766
PMCPMC7781537
OpenAlexW3116289303

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.