Blue-Print Autophagy in 2020: A Critical Review

Sergey A Dyshlovoy1

  • 1Laboratory of Pharmacology, A.V. Zhirmunsky National Scientific Center of Marine Biology, Far Eastern Branch, Russian Academy of Sciences, 690041 Vladivostok, Russia.

Marine Drugs
|September 24, 2020
PubMed

Insights

Marine natural compounds show potential for modulating autophagy, a key biological process. However, over half of compounds reviewed lack validated effects, highlighting the need for standardized experimental data interpretation in this field.

Area of Science:

  • Cellular biology
  • Pharmacology

Background:

  • Autophagy is a crucial cellular process with therapeutic potential for cancer and neurodegenerative diseases.
  • Marine natural compounds are increasingly investigated for their ability to modulate autophagy.
  • Challenges exist in current autophagy monitoring assays and data interpretation.

Purpose of the Study:

  • To review marine natural compounds reported to affect autophagy between 2016 and 2020.
  • To re-analyze published experimental data based on established autophagy research guidelines.
  • To identify compounds with validated versus non-validated autophagy modulatory effects.

Main Methods:

  • Literature review of marine natural compounds impacting autophagy (2016-2020).
  • Critical re-analysis of experimental data against Klionsky et al. guidelines.
  • Categorization of compounds into validated and non-validated autophagy modulators.

Main Results:

  • Over 50% of reported autophagy activators or inhibitors lacked validated effects.
  • Experimental data for many compounds were ambiguous, suggesting both activation and inhibition.
  • Compounds were classified into those with validated and non-validated autophagy modulatory effects.

Conclusions:

  • Standardization of experimental design and data interpretation is critical in autophagy research.
  • Many marine natural compounds require further investigation to confirm their autophagy modulatory roles.
  • The field needs rigorous validation to harness the therapeutic potential of autophagy-modulating compounds.

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