Evidence map›Paper›PMID 27077385›Full record

ArticlePLoS genetics2016

Intermittent Stem Cell Cycling Balances Self-Renewal and Senescence of the C. elegans Germ Line.

Amanda Cinquin, Michael Chiang, Adrian Paz, Sam Hallman, Oliver Yuan, Indre Vysniauskaite, Charless C Fowlkes, Olivier Cinquin

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

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  6. A male pheromone that improves the quality of the oogenic germline.Proceedings of the National Academy of Sciences of the United States of America · 2022
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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

8 authors at 1 institution in 1 country.

Amanda CinquinDepartment of Developmental & Cell Biology, University of California, Irvine, Irvine, California, United States of America.
Michael ChiangDepartment of Developmental & Cell Biology, University of California, Irvine, Irvine, California, United States of America.
Adrian PazDepartment of Developmental & Cell Biology, University of California, Irvine, Irvine, California, United States of America.
Sam HallmanCenter for Complex Biological Systems, University of California, Irvine, Irvine, California, United States of America.
Oliver YuanDepartment of Developmental & Cell Biology, University of California, Irvine, Irvine, California, United States of America.
Indre VysniauskaiteDepartment of Developmental & Cell Biology, University of California, Irvine, Irvine, California, United States of America.
Charless C FowlkesCenter for Complex Biological Systems, University of California, Irvine, Irvine, California, United States of America.
Olivier CinquinDepartment of Developmental & Cell Biology, University of California, Irvine, Irvine, California, United States of America.
University of California, Irvine · US

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Melanie Funes · 1994 to 2026
$57.9M
Uncover Strategies Used By Biological SystemsP50GM076516 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI GRATTON, ENRICO · 2007 to 2016
$25.1M
Biomedical Informatics Training ProgramT15LM007443 · NLM · UNIVERSITY OF CALIFORNIA-IRVINE · PI BALDI, PIERRE · 2002 to 2012
$9.3M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
Mathematical, Computational and Systems BiologyT32EB009418 · NIBIB · UNIVERSITY OF CALIFORNIA-IRVINE · PI LANDER, ARTHUR D, NIE, QING · 2009 to 2019
$2.4M
Control of cell cycling speed to delay the onset of senescenceR01GM102635 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI CINQUIN, OLIVIER · 2012 to 2016
$1.4M
Training Program in Systems Biology of DevelopmentT32HD060555 · NICHD · UNIVERSITY OF CALIFORNIA-IRVINE · PI LANDER, ARTHUR D · 2009 to 2013
$1.3M
Direct tests of the role of stem cells in minimizing mutation accumulationR21AG042125 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI CINQUIN, OLIVIER · 2012 to 2013
$396k
NCI NIH HHS P30 CA062203NIA NIH HHS R21 AG042125NIA NIH HHS R21-AG042125NIBIB NIH HHS T32 EB009418NIBIB NIH HHS T32-EB009418NICHD NIH HHS T32 HD060555NICHD NIH HHS T32-HD060555NIGMS NIH HHS P50 GM076516NIGMS NIH HHS P50-GM076516NIGMS NIH HHS R01 GM102635NIGMS NIH HHS R01-GM102635NIH HHS P40 OD010440NLM NIH HHS T15 LM007443NLM NIH HHS T15-LM007443
6 · The paper itself

Abstract

Self-renewing organs often experience a decline in function in the course of aging. It is unclear whether chronological age or external factors control this decline, or whether it is driven by stem cell self-renewal-for example, because cycling cells exhaust their replicative capacity and become senescent. Here we assay the relationship between stem cell cycling and senescence in the Caenorhabditis elegans reproductive system, defining this senescence as the progressive decline in "reproductive capacity," i.e. in the number of progeny that can be produced until cessation of reproduction. We show that stem cell cycling diminishes remaining reproductive capacity, at least in part through the DNA damage response. Paradoxically, gonads kept under conditions that preclude reproduction keep cycling and producing cells that undergo apoptosis or are laid as unfertilized gametes, thus squandering reproductive capacity. We show that continued activity is in fact beneficial inasmuch as gonads that are active when reproduction is initiated have more sustained early progeny production. Intriguingly, continued cycling is intermittent-gonads switch between active and dormant states-and in all likelihood stochastic. Other organs face tradeoffs whereby stem cell cycling has the beneficial effect of providing freshly-differentiated cells and the detrimental effect of increasing the likelihood of cancer or senescence; stochastic stem cell cycling may allow for a subset of cells to preserve proliferative potential in old age, which may implement a strategy to deal with uncertainty as to the total amount of proliferation to be undergone over an organism's lifespan.

Indexed as

AgingAnimalsApoptosisCaenorhabditis elegansCaenorhabditis elegans ProteinsCell Self RenewalCellular SenescenceDNA-Binding ProteinsDNA DamageDNA RepairFemaleM Phase Cell Cycle CheckpointsOvaryReplication Protein AReproductionStarvationCaenorhabditis elegans ProteinsDNA-Binding Proteinsfog-1 protein, C elegansfog-2 protein, C elegansReplication Protein ASPE-8 protein, C elegansTranscription Factors

Identifiers

PMID27077385
PMCPMC4831802
OpenAlexW2337811941

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.