The role of autophagy in cancer chemotherapy drug resistance

Detalhes bibliográficos
Autor(a) principal: Asoudeh, Monireh
Data de Publicação: 2022
Outros Autores: Dalhaimer, Paul
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://doi.org/10.48797/sl.2022.10
Resumo: About 650,000 cancer patients are treated with chemotherapy drugs each year. There have been tremendous advances in this field over the past several decades. However, major obstacles remain. One of these obstacles is that cancer cells become drug resistant. 90% of clinical failures in chemotherapy treatment are because of drug resistance. In this review, we focus on the role of autophagy in cancer cell drug resistance. In non-cancerous cells, autophagy is constitutively active, but can be augmented by nutrient deprivation, reactive oxygen species (ROS), and pathogen invasion. It can either keep cells alive or trigger apoptosis, depending on the degree of disruption of cell homeostasis. These are critical considerations in cancer treatment: autophagy can either kill cells or it can keep cancer cells alive, furthering drug resistance. In cancer cells, chemotherapy typically triggers ROS. ROS then activate autophagy through several pathways. Thus, understanding how autophagy works in cancer cells that have been exposed to drugs can be a valuable weapon to combat drug resistance.
id RCAP_d4405c55563088bf299d04e98c796ff9
oai_identifier_str oai:publicacoes.cespu.pt:article/10
network_acronym_str RCAP
network_name_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository_id_str 7160
spelling The role of autophagy in cancer chemotherapy drug resistanceautophagychemotherapydrug resistancecancerreactive oxygen speciesAbout 650,000 cancer patients are treated with chemotherapy drugs each year. There have been tremendous advances in this field over the past several decades. However, major obstacles remain. One of these obstacles is that cancer cells become drug resistant. 90% of clinical failures in chemotherapy treatment are because of drug resistance. In this review, we focus on the role of autophagy in cancer cell drug resistance. In non-cancerous cells, autophagy is constitutively active, but can be augmented by nutrient deprivation, reactive oxygen species (ROS), and pathogen invasion. It can either keep cells alive or trigger apoptosis, depending on the degree of disruption of cell homeostasis. These are critical considerations in cancer treatment: autophagy can either kill cells or it can keep cancer cells alive, furthering drug resistance. In cancer cells, chemotherapy typically triggers ROS. ROS then activate autophagy through several pathways. Thus, understanding how autophagy works in cancer cells that have been exposed to drugs can be a valuable weapon to combat drug resistance.IUCS-CESPU Publishing2022-05-13info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://doi.org/10.48797/sl.2022.10https://doi.org/10.48797/sl.2022.10Scientific Letters; Vol. 1 No. 1 (2022); 42795-5117reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPenghttps://publicacoes.cespu.pt/index.php/sl/article/view/10https://publicacoes.cespu.pt/index.php/sl/article/view/10/6Copyright (c) 2022 Monireh Asoudeh, Paul Dalhaimerinfo:eu-repo/semantics/openAccessAsoudeh, MonirehDalhaimer, Paul2023-04-22T08:45:12Zoai:publicacoes.cespu.pt:article/10Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:46:16.551683Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv The role of autophagy in cancer chemotherapy drug resistance
title The role of autophagy in cancer chemotherapy drug resistance
spellingShingle The role of autophagy in cancer chemotherapy drug resistance
Asoudeh, Monireh
autophagy
chemotherapy
drug resistance
cancer
reactive oxygen species
title_short The role of autophagy in cancer chemotherapy drug resistance
title_full The role of autophagy in cancer chemotherapy drug resistance
title_fullStr The role of autophagy in cancer chemotherapy drug resistance
title_full_unstemmed The role of autophagy in cancer chemotherapy drug resistance
title_sort The role of autophagy in cancer chemotherapy drug resistance
author Asoudeh, Monireh
author_facet Asoudeh, Monireh
Dalhaimer, Paul
author_role author
author2 Dalhaimer, Paul
author2_role author
dc.contributor.author.fl_str_mv Asoudeh, Monireh
Dalhaimer, Paul
dc.subject.por.fl_str_mv autophagy
chemotherapy
drug resistance
cancer
reactive oxygen species
topic autophagy
chemotherapy
drug resistance
cancer
reactive oxygen species
description About 650,000 cancer patients are treated with chemotherapy drugs each year. There have been tremendous advances in this field over the past several decades. However, major obstacles remain. One of these obstacles is that cancer cells become drug resistant. 90% of clinical failures in chemotherapy treatment are because of drug resistance. In this review, we focus on the role of autophagy in cancer cell drug resistance. In non-cancerous cells, autophagy is constitutively active, but can be augmented by nutrient deprivation, reactive oxygen species (ROS), and pathogen invasion. It can either keep cells alive or trigger apoptosis, depending on the degree of disruption of cell homeostasis. These are critical considerations in cancer treatment: autophagy can either kill cells or it can keep cancer cells alive, furthering drug resistance. In cancer cells, chemotherapy typically triggers ROS. ROS then activate autophagy through several pathways. Thus, understanding how autophagy works in cancer cells that have been exposed to drugs can be a valuable weapon to combat drug resistance.
publishDate 2022
dc.date.none.fl_str_mv 2022-05-13
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://doi.org/10.48797/sl.2022.10
https://doi.org/10.48797/sl.2022.10
url https://doi.org/10.48797/sl.2022.10
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://publicacoes.cespu.pt/index.php/sl/article/view/10
https://publicacoes.cespu.pt/index.php/sl/article/view/10/6
dc.rights.driver.fl_str_mv Copyright (c) 2022 Monireh Asoudeh, Paul Dalhaimer
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2022 Monireh Asoudeh, Paul Dalhaimer
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv IUCS-CESPU Publishing
publisher.none.fl_str_mv IUCS-CESPU Publishing
dc.source.none.fl_str_mv Scientific Letters; Vol. 1 No. 1 (2022); 4
2795-5117
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
_version_ 1799130934435381248