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Senescence-Associated miRNAs and Their Role in Pancreatic Cancer

Replicative senescence is irreversible cell proliferation arrest for somatic cells which can be circumvented in cancers. Cellular senescence is a process, which may play two opposite roles. On the one hand, this is a natural protection of somatic cells against unlimited proliferation and malignant t...

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Detalles Bibliográficos
Autores principales: Popov, Alexey, Mandys, Vaclav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9098800/
https://www.ncbi.nlm.nih.gov/pubmed/35570840
http://dx.doi.org/10.3389/pore.2022.1610156
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author Popov, Alexey
Mandys, Vaclav
author_facet Popov, Alexey
Mandys, Vaclav
author_sort Popov, Alexey
collection PubMed
description Replicative senescence is irreversible cell proliferation arrest for somatic cells which can be circumvented in cancers. Cellular senescence is a process, which may play two opposite roles. On the one hand, this is a natural protection of somatic cells against unlimited proliferation and malignant transformation. On the other hand, cellular secretion caused by senescence can stimulate inflammation and proliferation of adjacent cells that may promote malignancy. The main genes controlling the senescence pathways are also well known as tumor suppressors. Almost 140 genes regulate both cellular senescence and cancer pathways. About two thirds of these genes (64%) are regulated by microRNAs. Senescence-associated miRNAs can stimulate cancer progression or act as tumor suppressors. Here we review the role playing by senescence-associated miRNAs in development, diagnostics and treatment of pancreatic cancer.
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spelling pubmed-90988002022-05-14 Senescence-Associated miRNAs and Their Role in Pancreatic Cancer Popov, Alexey Mandys, Vaclav Pathol Oncol Res Pathology and Oncology Archive Replicative senescence is irreversible cell proliferation arrest for somatic cells which can be circumvented in cancers. Cellular senescence is a process, which may play two opposite roles. On the one hand, this is a natural protection of somatic cells against unlimited proliferation and malignant transformation. On the other hand, cellular secretion caused by senescence can stimulate inflammation and proliferation of adjacent cells that may promote malignancy. The main genes controlling the senescence pathways are also well known as tumor suppressors. Almost 140 genes regulate both cellular senescence and cancer pathways. About two thirds of these genes (64%) are regulated by microRNAs. Senescence-associated miRNAs can stimulate cancer progression or act as tumor suppressors. Here we review the role playing by senescence-associated miRNAs in development, diagnostics and treatment of pancreatic cancer. Frontiers Media S.A. 2022-04-29 /pmc/articles/PMC9098800/ /pubmed/35570840 http://dx.doi.org/10.3389/pore.2022.1610156 Text en Copyright © 2022 Popov and Mandys. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pathology and Oncology Archive
Popov, Alexey
Mandys, Vaclav
Senescence-Associated miRNAs and Their Role in Pancreatic Cancer
title Senescence-Associated miRNAs and Their Role in Pancreatic Cancer
title_full Senescence-Associated miRNAs and Their Role in Pancreatic Cancer
title_fullStr Senescence-Associated miRNAs and Their Role in Pancreatic Cancer
title_full_unstemmed Senescence-Associated miRNAs and Their Role in Pancreatic Cancer
title_short Senescence-Associated miRNAs and Their Role in Pancreatic Cancer
title_sort senescence-associated mirnas and their role in pancreatic cancer
topic Pathology and Oncology Archive
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9098800/
https://www.ncbi.nlm.nih.gov/pubmed/35570840
http://dx.doi.org/10.3389/pore.2022.1610156
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