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Autophagy modulation as a potential therapeutic target for diverse diseases

Open access
Rubinsztein, David C., Codogno, Patrice, Levine, Beth·2012·Nature Reviews Drug Discovery

Abstract

The lysosomal degradation pathway known as autophagy has an essential homeostatic role in controlling the quality of the cytoplasm. However, this pathway has also been implicated in the pathology of an array of human disorders. Here, Rubinsztein and colleagues provide an overview of the mechanisms and regulation of autophagy, discuss the role of this pathway in disease and highlight potential strategies for therapeutic modulation. Autophagy is an essential, conserved lysosomal degradation pathway that controls the quality of the cytoplasm by eliminating protein aggregates and damaged organelles. It begins when double-membraned autophagosomes engulf portions of the cytoplasm, which is followed by fusion of these vesicles with lysosomes and degradation of the autophagic contents. In addition to its vital homeostatic role, this degradation pathway is involved in various human disorders, including metabolic conditions, neurodegenerative diseases, cancers and infectious diseases. This article provides an overview of the mechanisms and regulation of autophagy, the role of this pathway in disease and strategies for therapeutic modulation.

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Metadata

Authors
Rubinsztein, D. C., Codogno, P., & Levine, B.
Venue
Nature Reviews Drug Discovery
Published
2012-08-31
Volume
11
Issue
9
Pages
709-730
ISSN
  • 1474-1776 (ISSN-L)
  • 1474-1784
OpenAlex
W1991692801
Cited by
1,437
References
72
FWCI
16.51
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Autophagy modulation as a potential therapeutic target for diverse diseases. https://app.cochat.ai/papers/10.1038/nrd3802
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Rubinsztein, D. C., Codogno, P., & Levine, B. (2012). Autophagy modulation as a potential therapeutic target for diverse diseases. Nature Reviews Drug Discovery. https://doi.org/10.1038/nrd3802

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.