» Articles » PMID: 30538986

Chemical Biology Strategies to Study Autophagy

Overview
Specialty Cell Biology
Date 2018 Dec 13
PMID 30538986
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Growing amount of evidence in the last two decades highlight that macroautophagy (generally referred to as autophagy) is not only indispensable for survival in yeast but also equally important to maintain cellular quality control in higher eukaryotes as well. Importantly, dysfunctional autophagy has been explicitly shown to be involved in various physiological and pathological conditions such as cell death, cancer, neurodegenerative, and other diseases. Therefore, modulation and regulation of the autophagy pathway has emerged as an alternative strategy for the treatment of various disease conditions in the recent years. Several studies have shown genetic or pharmacological modulation of autophagy to be effective in treating cancer, clearing intracellular aggregates and pathogens. Understanding and controlling the autophagic flux, either through a genetic or pharmacological approach is therefore a highly promising approach and of great scientific interest as spatiotemporal and cell-tissue-organ level autophagy regulation is not clearly understood. Indeed, chemical biology approaches that identify small molecule effectors of autophagy have thus a dual benefit: the modulators act as tools to study and understand the process of autophagy, and may also have therapeutic potential. In this review, we discuss different strategies that have appeared to screen and identify potent small molecule modulators of autophagy.

Citing Articles

Sodium butyrate exerts a neuroprotective effect in rats with acute carbon monoxide poisoning by activating autophagy through the mTOR signaling pathway.

Wen J, Xu Q, Li J, Shen X, Zhou X, Huang J Sci Rep. 2024; 14(1):4610.

PMID: 38409245 PMC: 10897214. DOI: 10.1038/s41598-024-55198-z.


The Role of iPSC Modeling Toward Projection of Autophagy Pathway in Disease Pathogenesis: Leader or Follower.

Kolahdouzmohammadi M, Totonchi M, Pahlavan S Stem Cell Rev Rep. 2020; 17(2):539-561.

PMID: 33245492 DOI: 10.1007/s12015-020-10077-8.


Cell Death Effects of the Phthalate 2-Ethyl-1-Hexanol on Human Linfoblast Cells.

Rios K, Velez C, Zayas B Open J Apoptosis. 2020; 8:1-15.

PMID: 33224640 PMC: 7678683. DOI: 10.4236/ojapo.2019.81001.


Chemical Screening Pipeline for Identification of Specific Plant Autophagy Modulators.

Dauphinee A, Cardoso C, Dalman K, Ohlsson J, Fick S, Robert S Plant Physiol. 2019; 181(3):855-866.

PMID: 31488572 PMC: 6836817. DOI: 10.1104/pp.19.00647.

References
1.
Dittmar A, Drozda A, Blader I . Drug Repurposing Screening Identifies Novel Compounds That Effectively Inhibit Toxoplasma gondii Growth. mSphere. 2016; 1(2). PMC: 4894684. DOI: 10.1128/mSphere.00042-15. View

2.
Mizushima N, Klionsky D . Protein turnover via autophagy: implications for metabolism. Annu Rev Nutr. 2007; 27:19-40. DOI: 10.1146/annurev.nutr.27.061406.093749. View

3.
Rosenberg L, Lafitte M, Grant W, Chen W, Cleveland J, Duckett D . Development of an HTS-Compatible Assay for the Discovery of Ulk1 Inhibitors. J Biomol Screen. 2015; 20(7):913-20. PMC: 4744088. DOI: 10.1177/1087057115579391. View

4.
Kolla L, Heo D, Rosenberg D, Barlow S, Maximova A, Cassio E . High content screen for identifying small-molecule LC3B-localization modulators in a renal cancer cell line. Sci Data. 2018; 5:180116. PMC: 6018519. DOI: 10.1038/sdata.2018.116. View

5.
Kunz J, Henriquez R, Schneider U, Movva N, Hall M . Target of rapamycin in yeast, TOR2, is an essential phosphatidylinositol kinase homolog required for G1 progression. Cell. 1993; 73(3):585-96. DOI: 10.1016/0092-8674(93)90144-f. View