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Targeting ATG4 in Cancer Therapy
Autophagy is a lysosome-mediated degradation pathway that enables the degradation and recycling of cytoplasmic components to sustain metabolic homoeostasis. Recently, autophagy has been reported to have an astonishing number of connections to cancer, as tumor cells require proficient autophagy in re...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562779/ https://www.ncbi.nlm.nih.gov/pubmed/31083460 http://dx.doi.org/10.3390/cancers11050649 |
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author | Fu, Yuanyuan Huang, Zhiying Hong, Liang Lu, Jia-Hong Feng, Du Yin, Xiao-Ming Li, Min |
author_facet | Fu, Yuanyuan Huang, Zhiying Hong, Liang Lu, Jia-Hong Feng, Du Yin, Xiao-Ming Li, Min |
author_sort | Fu, Yuanyuan |
collection | PubMed |
description | Autophagy is a lysosome-mediated degradation pathway that enables the degradation and recycling of cytoplasmic components to sustain metabolic homoeostasis. Recently, autophagy has been reported to have an astonishing number of connections to cancer, as tumor cells require proficient autophagy in response to metabolic and therapeutic stresses to sustain cell proliferation. Autophagy-related gene 4 (ATG4) is essential for autophagy by affecting autophagosome formation through processing full-length microtubule-associated protein 1A/1B-light chain 3 (pro-LC3) and lipidated LC3. An increasing amount of evidence suggests that ATG4B expression is elevated in certain types of cancer, implying that ATG4B is a potential anticancer target. In this review, we address the central roles of ATG4B in the autophagy machinery and in targeted cancer therapy. Specifically, we discuss how pharmacologically inhibiting ATG4B can benefit cancer therapies. |
format | Online Article Text |
id | pubmed-6562779 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-65627792019-06-17 Targeting ATG4 in Cancer Therapy Fu, Yuanyuan Huang, Zhiying Hong, Liang Lu, Jia-Hong Feng, Du Yin, Xiao-Ming Li, Min Cancers (Basel) Review Autophagy is a lysosome-mediated degradation pathway that enables the degradation and recycling of cytoplasmic components to sustain metabolic homoeostasis. Recently, autophagy has been reported to have an astonishing number of connections to cancer, as tumor cells require proficient autophagy in response to metabolic and therapeutic stresses to sustain cell proliferation. Autophagy-related gene 4 (ATG4) is essential for autophagy by affecting autophagosome formation through processing full-length microtubule-associated protein 1A/1B-light chain 3 (pro-LC3) and lipidated LC3. An increasing amount of evidence suggests that ATG4B expression is elevated in certain types of cancer, implying that ATG4B is a potential anticancer target. In this review, we address the central roles of ATG4B in the autophagy machinery and in targeted cancer therapy. Specifically, we discuss how pharmacologically inhibiting ATG4B can benefit cancer therapies. MDPI 2019-05-10 /pmc/articles/PMC6562779/ /pubmed/31083460 http://dx.doi.org/10.3390/cancers11050649 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Fu, Yuanyuan Huang, Zhiying Hong, Liang Lu, Jia-Hong Feng, Du Yin, Xiao-Ming Li, Min Targeting ATG4 in Cancer Therapy |
title | Targeting ATG4 in Cancer Therapy |
title_full | Targeting ATG4 in Cancer Therapy |
title_fullStr | Targeting ATG4 in Cancer Therapy |
title_full_unstemmed | Targeting ATG4 in Cancer Therapy |
title_short | Targeting ATG4 in Cancer Therapy |
title_sort | targeting atg4 in cancer therapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562779/ https://www.ncbi.nlm.nih.gov/pubmed/31083460 http://dx.doi.org/10.3390/cancers11050649 |
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