Evidence map›Paper›PMID 36123968›Full record

ArticleCell cycle (Georgetown, Tex.)2023

Mechanistic target of rapamycin (mTOR) regulates self-sustained quiescence, tumor indolence, and late clinical metastasis in a Beclin-1-dependent manner.

Carole Nicco, Marine Thomas, Julie Guillermet, Maryline Havard, Fanny Laurent-Tchenio, Ludivine Doridot, François Dautry, Frédéric Batteux, Thierry Tchenio

Open access · greenAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2023. 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 42% 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, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
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

9 authors at 1 institution in 1 country.

Carole NiccoInstitut Cochin, INSERM U1016/CNRS UMR 8104, Université de Paris, Paris, France.ORCID 0000-0001-8211-2556
Marine ThomasInstitut Cochin, INSERM U1016/CNRS UMR 8104, Université de Paris, Paris, France.ORCID 0000-0002-7007-0253
Julie GuillermetCentre de Recherches en Cancérologie de Toulouse (CRCT), Inserm U1037, CNRS U5071, Université Toulouse III, Toulouse, France.ORCID 0000-0003-3173-4907
Maryline HavardLaboratory of Biology and Applied Pharmacology (LBPA), CNRS UMR8113, IDA FR3242, ENS Paris-Saclay, Université Paris-Saclay, Gif-sur-Yvette, France.
Fanny Laurent-TchenioLaboratory of Biology and Applied Pharmacology (LBPA), CNRS UMR8113, IDA FR3242, ENS Paris-Saclay, Université Paris-Saclay, Gif-sur-Yvette, France.ORCID 0000-0002-4239-2423
Ludivine DoridotInstitut Cochin, INSERM U1016/CNRS UMR 8104, Université de Paris, Paris, France.ORCID 0000-0003-4380-1118
François DautryLaboratory of Biology and Applied Pharmacology (LBPA), CNRS UMR8113, IDA FR3242, ENS Paris-Saclay, Université Paris-Saclay, Gif-sur-Yvette, France.ORCID 0000-0003-4017-7452
Frédéric BatteuxInstitut Cochin, INSERM U1016/CNRS UMR 8104, Université de Paris, Paris, France.ORCID 0000-0002-1265-7996
Thierry TchenioInstitut Cochin, INSERM U1016/CNRS UMR 8104, Université de Paris, Paris, France.ORCID 0000-0002-6969-3138
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Self-sustained quiescence (SSQ) has been characterized as a stable but reversible non-proliferative cellular state that limits the cloning of cultured cancer cells. By developing refined clonogenic assays, we showed here that cancer cells in SSQ can be selected with anticancer agents and that culture at low cell density induced SSQ in pancreas and prostate adenocarcinoma cells. Pre-culture of cells in 3D or their pretreatment with pharmacological inhibitors of mechanistic target of rapamycin (mTOR) synergize with low cell density for induction of SSQ in a Beclin-1-dependent manner. Dissociated pancreatic adenocarcinoma (PAAD) cells rendered defective for SSQ by down-regulating Beclin-1 expression exhibit higher tumor growth rate when injected subcutaneously into mice. Conversely, dissociated PAAD cells in SSQ promote the formation of small indolent tumors that eventually transitioned to a rapid growth phase.

Indexed as

AdenocarcinomaPancreatic NeoplasmsAnimalsBeclin-1Cell Line, TumorCell ProliferationMaleMiceRNA, MessengerSirolimusTOR Serine-Threonine KinasesBeclin-1RNA, MessengerSirolimusTOR Serine-Threonine KinasesCancer cell persistenceclonogenicitydrug resistanceepithelial-mesenchymal transitionpancreas adenocarcinomaprostate adenocarcinoma

Identifiers

PMID36123968
PMCPMC9928463
OpenAlexW4296390232

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.