Evidence map›Paper›PMID 30197240›Full record

ArticleDevelopmental cell2018

Opposing Action of Hedgehog and Insulin Signaling Balances Proliferation and Autophagy to Determine Follicle Stem Cell Lifespan.

Tanu Singh, Eric H Lee, Tiffiney R Hartman, Dara M Ruiz-Whalen, Alana M O'Reilly

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. A decline in follicle cell function is a major driver ofbioRxiv : the preprint server for biology · 2026
    Article
  3. Starve-Feed Cycles Direct Quiescence to Proliferation Transitions inbioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. Article
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  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Autophagy in Drosophila and Zebrafish.Advances in experimental medicine and biology · 2021
    Article
  16. Article
  17. Review
  18. Article
  19. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Tanu SinghDepartment of Molecular Therapeutics, Fox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, PA 19111, USA; Department of Biochemistry and Molecular Biology, Drexel University College of Medicine, Philadelphia, PA 19111, USA.
Eric H LeeDepartment of Molecular Therapeutics, Fox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, PA 19111, USA.
Tiffiney R HartmanDepartment of Molecular Therapeutics, Fox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, PA 19111, USA.
Dara M Ruiz-WhalenDepartment of Molecular Therapeutics, Fox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, PA 19111, USA.
Alana M O'ReillyDepartment of Molecular Therapeutics, Fox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, PA 19111, USA. Electronic address: alana.oreilly@fccc.edu.
Fox Chase Cancer Center · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Margaret von Mehren · 1985 to 2026
$138.8M
Drosophila Transgenic RNAi Resource ProjectR01GM084947 · NIGMS · HARVARD MEDICAL SCHOOL · PI PERRIMON, NORBERT · 2008 to 2019
$9.8M
Mechanisms Controlling Epithelial HomeostasisR01HD065800 · NICHD · RESEARCH INST OF FOX CHASE CAN CTR · PI O'REILLY, ALANA M · 2010 to 2020
$3.9M
NCI NIH HHS P30 CA006927NICHD NIH HHS R01 HD065800NIGMS NIH HHS R01 GM084947
6 · The paper itself

Abstract

Egg production declines with age in many species, a process linked with stem cell loss. Diet-dependent signaling has emerged as critical for stem cell maintenance during aging. Follicle stem cells (FSCs) in the Drosophila ovary are exquisitely responsive to diet-induced signals including Hedgehog (Hh) and insulin-IGF signaling (IIS), entering quiescence in the absence of nutrients and initiating proliferation rapidly upon feeding. Although highly proliferative FSCs generally exhibit an extended lifespan, we find that constitutive Hh signaling drives FSC loss and premature sterility despite high proliferative rates. This occurs due to Hh-mediated induction of autophagy in FSCs via a Ptc-dependent, Smo-independent mechanism. Hh-dependent autophagy increases during aging, triggering FSC loss and consequent reproductive arrest. IIS is necessary and sufficient to suppress Hh-induced autophagy, promoting a stable proliferative state. These results suggest that opposing action of diet-responsive IIS and Hh signals determine reproductive lifespan by modulating the proliferation-autophagy balance in FSCs during aging.

Indexed as

AutophagyCell ProliferationAnimalsDrosophila melanogasterDrosophila ProteinsFemaleHedgehog ProteinsHypoglycemic AgentsInsulinInsulin-Like Growth Factor IMaleOvarian FollicleReceptors, Cell SurfaceSignal TransductionSmoothened ReceptorStem Cell NicheDrosophila ProteinsHedgehog Proteinshh protein, DrosophilaHypoglycemic AgentsInsulinInsulin-Like Growth Factor Iptc protein, DrosophilaReceptors, Cell SurfaceSmoothened Receptorsmo protein, Drosophilaagingautophagydietfertilityfollicle stem cellHedgehoginsulinnutrient signalingpatchedstem cells

Identifiers

PMID30197240
PMCPMC6159899
OpenAlexW2891328856

What OpenQuestion holds

Textmetadata
LicenceTDM
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.