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The Role of Phosphatidylinositol 3-Kinase Catalytic Subunit Type 3 in the Pathogenesis of Human Cancer
Phosphatidylinositol 3-kinase catalytic subunit type 3 (PIK3C3), the mammalian ortholog of yeast vesicular protein sorting 34 (Vps34), belongs to the phosphoinositide 3-kinase (PI3K) family. PIK3C3 can phosphorylate phosphatidylinositol (PtdIns) to generate phosphatidylinositol 3-phosphate (PI3P), a...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535862/ https://www.ncbi.nlm.nih.gov/pubmed/34681622 http://dx.doi.org/10.3390/ijms222010964 |
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author | Chu, Chien-An Wang, Yi-Wen Chen, Yi-Lin Chen, Hui-Wen Chuang, Jing-Jing Chang, Hong-Yi Ho, Chung-Liang Chang, Chen Chow, Nan-Haw Lee, Chung-Ta |
author_facet | Chu, Chien-An Wang, Yi-Wen Chen, Yi-Lin Chen, Hui-Wen Chuang, Jing-Jing Chang, Hong-Yi Ho, Chung-Liang Chang, Chen Chow, Nan-Haw Lee, Chung-Ta |
author_sort | Chu, Chien-An |
collection | PubMed |
description | Phosphatidylinositol 3-kinase catalytic subunit type 3 (PIK3C3), the mammalian ortholog of yeast vesicular protein sorting 34 (Vps34), belongs to the phosphoinositide 3-kinase (PI3K) family. PIK3C3 can phosphorylate phosphatidylinositol (PtdIns) to generate phosphatidylinositol 3-phosphate (PI3P), a phospholipid central to autophagy. Inhibition of PIK3C3 successfully inhibits autophagy. Autophagy maintains cell survival when modifications occur in the cellular environment and helps tumor cells resist metabolic stress and cancer treatment. In addition, PIK3C3 could induce oncogenic transformation and enhance tumor cell proliferation, growth, and invasion through mechanisms independent of autophagy. This review addresses the structural and functional features, tissue distribution, and expression pattern of PIK3C3 in a variety of human tumors and highlights the underlying mechanisms involved in carcinogenesis. The implications in cancer biology, patient prognosis prediction, and cancer therapy are discussed. Altogether, the discovery of pharmacological inhibitors of PIK3C3 could reveal novel strategies for improving treatment outcomes for PIK3C3-mediated human diseases. |
format | Online Article Text |
id | pubmed-8535862 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85358622021-10-23 The Role of Phosphatidylinositol 3-Kinase Catalytic Subunit Type 3 in the Pathogenesis of Human Cancer Chu, Chien-An Wang, Yi-Wen Chen, Yi-Lin Chen, Hui-Wen Chuang, Jing-Jing Chang, Hong-Yi Ho, Chung-Liang Chang, Chen Chow, Nan-Haw Lee, Chung-Ta Int J Mol Sci Review Phosphatidylinositol 3-kinase catalytic subunit type 3 (PIK3C3), the mammalian ortholog of yeast vesicular protein sorting 34 (Vps34), belongs to the phosphoinositide 3-kinase (PI3K) family. PIK3C3 can phosphorylate phosphatidylinositol (PtdIns) to generate phosphatidylinositol 3-phosphate (PI3P), a phospholipid central to autophagy. Inhibition of PIK3C3 successfully inhibits autophagy. Autophagy maintains cell survival when modifications occur in the cellular environment and helps tumor cells resist metabolic stress and cancer treatment. In addition, PIK3C3 could induce oncogenic transformation and enhance tumor cell proliferation, growth, and invasion through mechanisms independent of autophagy. This review addresses the structural and functional features, tissue distribution, and expression pattern of PIK3C3 in a variety of human tumors and highlights the underlying mechanisms involved in carcinogenesis. The implications in cancer biology, patient prognosis prediction, and cancer therapy are discussed. Altogether, the discovery of pharmacological inhibitors of PIK3C3 could reveal novel strategies for improving treatment outcomes for PIK3C3-mediated human diseases. MDPI 2021-10-11 /pmc/articles/PMC8535862/ /pubmed/34681622 http://dx.doi.org/10.3390/ijms222010964 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Chu, Chien-An Wang, Yi-Wen Chen, Yi-Lin Chen, Hui-Wen Chuang, Jing-Jing Chang, Hong-Yi Ho, Chung-Liang Chang, Chen Chow, Nan-Haw Lee, Chung-Ta The Role of Phosphatidylinositol 3-Kinase Catalytic Subunit Type 3 in the Pathogenesis of Human Cancer |
title | The Role of Phosphatidylinositol 3-Kinase Catalytic Subunit Type 3 in the Pathogenesis of Human Cancer |
title_full | The Role of Phosphatidylinositol 3-Kinase Catalytic Subunit Type 3 in the Pathogenesis of Human Cancer |
title_fullStr | The Role of Phosphatidylinositol 3-Kinase Catalytic Subunit Type 3 in the Pathogenesis of Human Cancer |
title_full_unstemmed | The Role of Phosphatidylinositol 3-Kinase Catalytic Subunit Type 3 in the Pathogenesis of Human Cancer |
title_short | The Role of Phosphatidylinositol 3-Kinase Catalytic Subunit Type 3 in the Pathogenesis of Human Cancer |
title_sort | role of phosphatidylinositol 3-kinase catalytic subunit type 3 in the pathogenesis of human cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535862/ https://www.ncbi.nlm.nih.gov/pubmed/34681622 http://dx.doi.org/10.3390/ijms222010964 |
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