Evidence map›Paper›PMID 30744021›Full record

ReviewInternational journal of molecular sciences2019

Targeting Autophagy to Overcome Human Diseases.

Maria Condello, Evelin Pellegrini, Michele Caraglia, Stefania Meschini

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing 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

65 citing papers in PubMed.

  1. Article
  2. Pharmaceutics · 2026
    Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Cloning and Identification of Common Carp (Current issues in molecular biology · 2024
    Article
  9. The role of PI3K/Akt signaling pathway in chronic kidney disease.International urology and nephrology · 2024
    Review
  10. Characteristics and significance of programmed cell death-related gene expression signature in skin cutaneous melanoma.Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) · 2024
    Article
  11. OncolyticTurkish journal of haematology : official journal of Turkish Society of Haematology · 2024
    Article
  12. Article
  13. Review
  14. Article
  15. Liver Iron Loading in Alcohol-Associated Liver Disease.The American journal of pathology · 2023
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

5 more citing papers are in PubMed but not listed here.

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.

Maria CondelloNational Center for Drug Research and Evaluation, National Institute of Health, Viale Regina Elena, 00161 Rome, Italy. maria.condello@iss.it.
Evelin PellegriniNational Center for Drug Research and Evaluation, National Institute of Health, Viale Regina Elena, 00161 Rome, Italy. evelin.pellegrini@guest.iss.it.
Michele CaragliaDepartment of Precision Medicine, University of Campania "Luigi Vanvitelli", 80138 Naples, Italy. michele.caraglia@unicampania.it.
Stefania MeschiniNational Center for Drug Research and Evaluation, National Institute of Health, Viale Regina Elena, 00161 Rome, Italy. stefania.meschini@iss.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy is an evolutionarily conserved cellular process, through which damaged organelles and superfluous proteins are degraded, for maintaining the correct cellular balance during stress insult. It involves formation of double-membrane vesicles, named autophagosomes, that capture cytosolic cargo and deliver it to lysosomes, where the breakdown products are recycled back to cytoplasm. On the basis of degraded cell components, some selective types of autophagy can be identified (mitophagy, ribophagy, reticulophagy, lysophagy, pexophagy, lipophagy, and glycophagy). Dysregulation of autophagy can induce various disease manifestations, such as inflammation, aging, metabolic diseases, neurodegenerative disorders and cancer. The understanding of the molecular mechanism that regulates the different phases of the autophagic process and the role in the development of diseases are only in an early stage. There are still questions that must be answered concerning the functions of the autophagy-related proteins. In this review, we describe the principal cellular and molecular autophagic functions, selective types of autophagy and the main in vitro methods to detect the role of autophagy in the cellular physiology. We also summarize the importance of the autophagic behavior in some diseases to provide a novel insight for target therapies.

Indexed as

Disease SusceptibilityMolecular Targeted TherapyAgingAnimalsApoptosisAutoimmune DiseasesAutophagyAutophagy-Related ProteinsHumansInflammationMetabolic SyndromeNecrosisNeoplasmsNeurodegenerative DiseasesSignal TransductionAutophagy-Related Proteinsagingautoimmune diseasesautophagycancercell deathcell survivalinflammationmetabolic diseasesneurodegenerative diseasestarget therapy

Identifiers

PMID30744021
PMCPMC6387456

What OpenQuestion holds

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LicenceCC BY
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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.