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The Dual Role of PDCD10 in Cancers: A Promising Therapeutic Target

SIMPLE SUMMARY: As an adaptor protein, PDCD10 is involved in regulation of diverse biological processes by interacting with multiple molecules. Recently, growing amounts of studies have focused on function of PDCD10 in cancers. However, PDCD10 seems to have a dual role (either pro- or anti-tumor eff...

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Autores principales: Liu, Jingdian, Zhao, Kai, Wu, Sisi, Li, Chaoxi, You, Chao, Wang, Junwen, Shu, Kai, Lei, Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9740655/
https://www.ncbi.nlm.nih.gov/pubmed/36497468
http://dx.doi.org/10.3390/cancers14235986
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author Liu, Jingdian
Zhao, Kai
Wu, Sisi
Li, Chaoxi
You, Chao
Wang, Junwen
Shu, Kai
Lei, Ting
author_facet Liu, Jingdian
Zhao, Kai
Wu, Sisi
Li, Chaoxi
You, Chao
Wang, Junwen
Shu, Kai
Lei, Ting
author_sort Liu, Jingdian
collection PubMed
description SIMPLE SUMMARY: As an adaptor protein, PDCD10 is involved in regulation of diverse biological processes by interacting with multiple molecules. Recently, growing amounts of studies have focused on function of PDCD10 in cancers. However, PDCD10 seems to have a dual role (either pro- or anti-tumor effects) in various cancer types, which may depend on cell/tissue specificity with different cellular interactors. In this review, we provided an overview of the structure and molecular functions of PDCD10, and summarized the knowledge of the dual role of PDCD10 in cancers, with a view to future development and application of PDCD10 as a clinical therapeutic target in cancers. ABSTRACT: Programmed cell death 10 (PDCD10) was initially considered as a protein associated with apoptosis. However, recent studies showed that PDCD10 is actually an adaptor protein. By interacting with multiple molecules, PDCD10 participates in various physiological processes, such as cell survival, migration, cell differentiation, vesicle trafficking, cellular senescence, neurovascular development, and gonadogenesis. Moreover, over the past few decades, accumulating evidence has demonstrated that the aberrant expression or mutation of PDCD10 is extremely common in various pathological processes, especially in cancers. The dysfunction of PDCD10 has been strongly implicated in oncogenesis and tumor progression. However, the updated data seem to indicate that PDCD10 has a dual role (either pro- or anti-tumor effects) in various cancer types, depending on cell/tissue specificity with different cellular interactors. In this review, we aimed to summarize the knowledge of the dual role of PDCD10 in cancers with a special focus on its cellular function and potential molecular mechanism. With these efforts, we hoped to provide new insight into the future development and application of PDCD10 as a clinical therapeutic target in cancers.
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spelling pubmed-97406552022-12-11 The Dual Role of PDCD10 in Cancers: A Promising Therapeutic Target Liu, Jingdian Zhao, Kai Wu, Sisi Li, Chaoxi You, Chao Wang, Junwen Shu, Kai Lei, Ting Cancers (Basel) Review SIMPLE SUMMARY: As an adaptor protein, PDCD10 is involved in regulation of diverse biological processes by interacting with multiple molecules. Recently, growing amounts of studies have focused on function of PDCD10 in cancers. However, PDCD10 seems to have a dual role (either pro- or anti-tumor effects) in various cancer types, which may depend on cell/tissue specificity with different cellular interactors. In this review, we provided an overview of the structure and molecular functions of PDCD10, and summarized the knowledge of the dual role of PDCD10 in cancers, with a view to future development and application of PDCD10 as a clinical therapeutic target in cancers. ABSTRACT: Programmed cell death 10 (PDCD10) was initially considered as a protein associated with apoptosis. However, recent studies showed that PDCD10 is actually an adaptor protein. By interacting with multiple molecules, PDCD10 participates in various physiological processes, such as cell survival, migration, cell differentiation, vesicle trafficking, cellular senescence, neurovascular development, and gonadogenesis. Moreover, over the past few decades, accumulating evidence has demonstrated that the aberrant expression or mutation of PDCD10 is extremely common in various pathological processes, especially in cancers. The dysfunction of PDCD10 has been strongly implicated in oncogenesis and tumor progression. However, the updated data seem to indicate that PDCD10 has a dual role (either pro- or anti-tumor effects) in various cancer types, depending on cell/tissue specificity with different cellular interactors. In this review, we aimed to summarize the knowledge of the dual role of PDCD10 in cancers with a special focus on its cellular function and potential molecular mechanism. With these efforts, we hoped to provide new insight into the future development and application of PDCD10 as a clinical therapeutic target in cancers. MDPI 2022-12-03 /pmc/articles/PMC9740655/ /pubmed/36497468 http://dx.doi.org/10.3390/cancers14235986 Text en © 2022 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
Liu, Jingdian
Zhao, Kai
Wu, Sisi
Li, Chaoxi
You, Chao
Wang, Junwen
Shu, Kai
Lei, Ting
The Dual Role of PDCD10 in Cancers: A Promising Therapeutic Target
title The Dual Role of PDCD10 in Cancers: A Promising Therapeutic Target
title_full The Dual Role of PDCD10 in Cancers: A Promising Therapeutic Target
title_fullStr The Dual Role of PDCD10 in Cancers: A Promising Therapeutic Target
title_full_unstemmed The Dual Role of PDCD10 in Cancers: A Promising Therapeutic Target
title_short The Dual Role of PDCD10 in Cancers: A Promising Therapeutic Target
title_sort dual role of pdcd10 in cancers: a promising therapeutic target
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9740655/
https://www.ncbi.nlm.nih.gov/pubmed/36497468
http://dx.doi.org/10.3390/cancers14235986
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