Evidence map›Paper›PMID 34832087›Full record

ReviewMembranes2021

The mTOR Pathway in Pluripotent Stem Cells: Lessons for Understanding Cancer Cell Dormancy.

Bashar A Alhasan, Sergei A Gordeev, Aleksandra R Knyazeva, Kseniia V Aleksandrova, Boris A Margulis, Irina V Guzhova, Irina I Suvorova

Open access · goldAbstract readReview
In one paragraph

Review in Membranes, 2021. 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
1.4field-weighted citation impact, top 19% 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, 18 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

7 authors at 1 institution in 1 country.

Bashar A AlhasanInstitute of Cytology, Russian Academy of Sciences, 194064 St. Petersburg, Russia.ORCID 0000-0002-2239-2872
Sergei A GordeevInstitute of Cytology, Russian Academy of Sciences, 194064 St. Petersburg, Russia.
Aleksandra R KnyazevaInstitute of Cytology, Russian Academy of Sciences, 194064 St. Petersburg, Russia.ORCID 0000-0002-0447-5447
Kseniia V AleksandrovaInstitute of Cytology, Russian Academy of Sciences, 194064 St. Petersburg, Russia.
Boris A MargulisInstitute of Cytology, Russian Academy of Sciences, 194064 St. Petersburg, Russia.
Irina V GuzhovaInstitute of Cytology, Russian Academy of Sciences, 194064 St. Petersburg, Russia.ORCID 0000-0002-8775-7713
Irina I SuvorovaInstitute of Cytology, Russian Academy of Sciences, 194064 St. Petersburg, Russia.ORCID 0000-0001-7992-2435
Institute of Cytology · RU

Funding

the Ministry of Science and Higher Education Russian Federation № 075-15-2020-773
6 · The paper itself

Abstract

Currently, the success of targeted anticancer therapies largely depends on the correct understanding of the dormant state of cancer cells, since it is increasingly regarded to fuel tumor recurrence. The concept of cancer cell dormancy is often considered as an adaptive response of cancer cells to stress, and, therefore, is limited. It is possible that the cancer dormant state is not a privilege of cancer cells but the same reproductive survival strategy as diapause used by embryonic stem cells (ESCs). Recent advances reveal that high autophagy and mTOR pathway reduction are key mechanisms contributing to dormancy and diapause. ESCs, sharing their main features with cancer stem cells, have a delicate balance between the mTOR pathway and autophagy activity permissive for diapause induction. In this review, we discuss the functioning of the mTOR signaling and autophagy in ESCs in detail that allows us to deepen our understanding of the biology of cancer cell dormancy.

Indexed as

autophagycancer cell dormancyembryonic diapauseembryonic stem cellsmTORpluripotencypluripotent stem cells

Identifiers

PMID34832087
PMCPMC8620939
OpenAlexW3211711196

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.