Evidence map›Paper›PMID 26759963›Full record

ArticleAutophagy2016

Autophagy and modular restructuring of metabolism control germline tumor differentiation and proliferation in C. elegans.

Ligia C Gomes, Devang Odedra, Ivan Dikic, Christian Pohl

Abstract read
In one paragraph

Article in Autophagy, 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
–field-weighted citation impact
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.

  1. Article
  2. ConsideringCells · 2024
    Review
  3. Article
  4. Article
  5. Article
  6. Long non-coding RNARNA biology · 2020
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Role of Hypoxia-Inducible Factors 1α (HIF1α) in SH-SY5Y Cell Autophagy Induced by Oxygen-Glucose Deprivation.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  13. Article
  14. Article
  15. Review
  16. Article
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

4 authors.

Ligia C Gomesa Buchmann Institute for Molecular Life Sciences, Goethe University , Frankfurt (Main) , Germany.
Devang Odedraa Buchmann Institute for Molecular Life Sciences, Goethe University , Frankfurt (Main) , Germany.
Ivan Dikica Buchmann Institute for Molecular Life Sciences, Goethe University , Frankfurt (Main) , Germany.
Christian Pohla Buchmann Institute for Molecular Life Sciences, Goethe University , Frankfurt (Main) , Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy can act either as a tumor suppressor or as a survival mechanism for established tumors. To understand how autophagy plays this dual role in cancer, in vivo models are required. By using a highly heterogeneous C. elegans germline tumor, we show that autophagy-related proteins are expressed in a specific subset of tumor cells, neurons. Inhibition of autophagy impairs neuronal differentiation and increases tumor cell number, resulting in a shorter life span of animals with tumors, while induction of autophagy extends their life span by impairing tumor proliferation. Fasting of animals with fully developed tumors leads to a doubling of their life span, which depends on modular changes in transcription including switches in transcription factor networks and mitochondrial metabolism. Hence, our results suggest that metabolic restructuring, cell-type specific regulation of autophagy and neuronal differentiation constitute central pathways preventing growth of heterogeneous tumors.

Indexed as

AutophagyCell DifferentiationAnimalsApoptosisCaenorhabditis elegansCaenorhabditis elegans ProteinsCell ProliferationFastingGene Expression RegulationGene Regulatory NetworksGerm CellsLongevityMitochondriaNeoplasmsNeuronsReactive Oxygen SpeciesCaenorhabditis elegans ProteinsReactive Oxygen SpeciesAutophagyC. elegansdifferentiationfastinglife spanmetabolismnuclear hormone receptorsROSstress responseteratoma

Identifiers

PMID26759963
PMCPMC4835962

What OpenQuestion holds

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LicenceCC BY-NC
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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.