Evidence map›Paper›PMID 26636375›Full record

ArticleCell cycle (Georgetown, Tex.)2016

Tetraploidization or autophagy: The ultimate fate of senescent human endometrial stem cells under ATM or p53 inhibition.

Aleksandra V Borodkina, Alla N Shatrova, Pavel I Deryabin, Anastasiya A Grukova, Nikolay N Nikolsky, Elena B Burova

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 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

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  14. The evolutionary significance of polyploidy.Nature reviews. Genetics · 2017
    Review
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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 1 institution in 1 country.

Aleksandra V Borodkinaa Department of Intracellular Signaling and Transport , Institute of Cytology, Russian Academy of Sciences , St. Petersburg , Russia.
Alla N Shatrovaa Department of Intracellular Signaling and Transport , Institute of Cytology, Russian Academy of Sciences , St. Petersburg , Russia.
Pavel I Deryabina Department of Intracellular Signaling and Transport , Institute of Cytology, Russian Academy of Sciences , St. Petersburg , Russia.
Anastasiya A Grukovaa Department of Intracellular Signaling and Transport , Institute of Cytology, Russian Academy of Sciences , St. Petersburg , Russia.
Nikolay N Nikolskya Department of Intracellular Signaling and Transport , Institute of Cytology, Russian Academy of Sciences , St. Petersburg , Russia.
Elena B Burovaa Department of Intracellular Signaling and Transport , Institute of Cytology, Russian Academy of Sciences , St. Petersburg , Russia.
Institute of Cytology · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previously we demonstrated that endometrium-derived human mesenchymal stem cells (hMESCs) via activation of the ATM/p53/p21/Rb pathway enter the premature senescence in response to oxidative stress. Down regulation effects of the key components of this signaling pathway, particularly ATM and p53, on a fate of stressed hMESCs have not yet been investigated. In the present study by using the specific inhibitors Ku55933 and Pifithrin-α, we confirmed implication of both ATM and p53 in H(2)O(2)-induced senescence of hMESCs. ATM or p53 down regulation was shown to modulate differently the cellular fate of H(2)O(2)-treated hMESCs. ATM inhibition allowed H(2)O(2)-stimulated hMESCs to escape the permanent cell cycle arrest due to loss of the functional ATM/p53/p21/Rb pathway, and induced bypass of mitosis and re-entry into S phase, resulting in tetraploid cells. On the contrary, suppression of the p53 transcriptional activity caused a pronounced cell death of H(2)O(2)-treated hMESCs via autophagy induction. The obtained data clearly demonstrate that down regulation of ATM or p53 shifts senescence of human endometrial stem cells toward tetraploidization or autophagy.

Indexed as

TetraploidyAtaxia Telangiectasia Mutated ProteinsAutophagyCell SurvivalCellular SenescenceEndometriumFemaleHumansHydrogen PeroxideMesenchymal Stem CellsMorpholinesPyronesTumor Suppressor Protein p532-morpholin-4-yl-6-thianthren-1-yl-pyran-4-oneAtaxia Telangiectasia Mutated ProteinsATM protein, humanHydrogen PeroxideMorpholinesPyronesTumor Suppressor Protein p53ATM kinaseautophagycellular senescenceoxidative stressp53stem cellstetraploidization

Identifiers

PMID26636375
PMCPMC4825783
OpenAlexW2279261947

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.