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Nrf2 Signaling Pathway in Chemoprotection and Doxorubicin Resistance: Potential Application in Drug Discovery
Doxorubicin (DOX) is extensively applied in cancer therapy due to its efficacy in suppressing cancer progression and inducing apoptosis. After its discovery, this chemotherapeutic agent has been frequently used for cancer therapy, leading to chemoresistance. Due to dose-dependent toxicity, high conc...
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Published in: | Antioxidants 2021-02, Vol.10 (3), p.349 |
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creator | Mirzaei, Sepideh Zarrabi, Ali Hashemi, Farid Zabolian, Amirhossein Saleki, Hossein Azami, Negar Hamzehlou, Soodeh Farahani, Mahdi Vasheghani Hushmandi, Kiavash Ashrafizadeh, Milad Khan, Haroon Kumar, Alan Prem |
description | Doxorubicin (DOX) is extensively applied in cancer therapy due to its efficacy in suppressing cancer progression and inducing apoptosis. After its discovery, this chemotherapeutic agent has been frequently used for cancer therapy, leading to chemoresistance. Due to dose-dependent toxicity, high concentrations of DOX cannot be administered to cancer patients. Therefore, experiments have been directed towards revealing underlying mechanisms responsible for DOX resistance and ameliorating its adverse effects. Nuclear factor erythroid 2-related factor 2 (Nrf2) signaling is activated to increase levels of reactive oxygen species (ROS) in cells to protect them against oxidative stress. It has been reported that Nrf2 activation is associated with drug resistance. In cells exposed to DOX, stimulation of Nrf2 signaling protects cells against cell death. Various upstream mediators regulate Nrf2 in DOX resistance. Strategies, both pharmacological and genetic interventions, have been applied for reversing DOX resistance. However, Nrf2 induction is of importance for alleviating side effects of DOX. Pharmacological agents with naturally occurring compounds as the most common have been used for inducing Nrf2 signaling in DOX amelioration. Furthermore, signaling networks in which Nrf2 is a key player for protection against DOX adverse effects have been revealed and are discussed in the current review. |
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After its discovery, this chemotherapeutic agent has been frequently used for cancer therapy, leading to chemoresistance. Due to dose-dependent toxicity, high concentrations of DOX cannot be administered to cancer patients. Therefore, experiments have been directed towards revealing underlying mechanisms responsible for DOX resistance and ameliorating its adverse effects. Nuclear factor erythroid 2-related factor 2 (Nrf2) signaling is activated to increase levels of reactive oxygen species (ROS) in cells to protect them against oxidative stress. It has been reported that Nrf2 activation is associated with drug resistance. In cells exposed to DOX, stimulation of Nrf2 signaling protects cells against cell death. Various upstream mediators regulate Nrf2 in DOX resistance. Strategies, both pharmacological and genetic interventions, have been applied for reversing DOX resistance. However, Nrf2 induction is of importance for alleviating side effects of DOX. Pharmacological agents with naturally occurring compounds as the most common have been used for inducing Nrf2 signaling in DOX amelioration. Furthermore, signaling networks in which Nrf2 is a key player for protection against DOX adverse effects have been revealed and are discussed in the current review.</description><identifier>ISSN: 2076-3921</identifier><identifier>EISSN: 2076-3921</identifier><identifier>DOI: 10.3390/antiox10030349</identifier><identifier>PMID: 33652780</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Antioxidants ; Apoptosis ; Brain cancer ; Cancer ; Cancer therapies ; cancer therapy ; Cell death ; Chemoprotection ; Chemoresistance ; Chemotherapy ; Doxorubicin ; Drug dosages ; Drug resistance ; Experiments ; Free radicals ; Hypoxia ; Inflammation ; Kinases ; Medical prognosis ; nuclear factor erythroid 2-related factor 2 (Nrf2) ; Oxidative stress ; Proteins ; Reactive oxygen species ; redox signaling ; Review ; Side effects ; Signal transduction ; Toxicity</subject><ispartof>Antioxidants, 2021-02, Vol.10 (3), p.349</ispartof><rights>2021 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/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 by the authors. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c484t-46e6dff81fff57e7cdc5e1fc0e1429109ebe976628c62c556b2bc91c040a7f503</citedby><cites>FETCH-LOGICAL-c484t-46e6dff81fff57e7cdc5e1fc0e1429109ebe976628c62c556b2bc91c040a7f503</cites><orcidid>0000-0003-0391-1769 ; 0000-0002-3754-5712 ; 0000-0001-6605-822X ; 0000-0001-9901-9534</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2524418801/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2524418801?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33652780$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mirzaei, Sepideh</creatorcontrib><creatorcontrib>Zarrabi, Ali</creatorcontrib><creatorcontrib>Hashemi, Farid</creatorcontrib><creatorcontrib>Zabolian, Amirhossein</creatorcontrib><creatorcontrib>Saleki, Hossein</creatorcontrib><creatorcontrib>Azami, Negar</creatorcontrib><creatorcontrib>Hamzehlou, Soodeh</creatorcontrib><creatorcontrib>Farahani, Mahdi Vasheghani</creatorcontrib><creatorcontrib>Hushmandi, Kiavash</creatorcontrib><creatorcontrib>Ashrafizadeh, Milad</creatorcontrib><creatorcontrib>Khan, Haroon</creatorcontrib><creatorcontrib>Kumar, Alan Prem</creatorcontrib><title>Nrf2 Signaling Pathway in Chemoprotection and Doxorubicin Resistance: Potential Application in Drug Discovery</title><title>Antioxidants</title><addtitle>Antioxidants (Basel)</addtitle><description>Doxorubicin (DOX) is extensively applied in cancer therapy due to its efficacy in suppressing cancer progression and inducing apoptosis. After its discovery, this chemotherapeutic agent has been frequently used for cancer therapy, leading to chemoresistance. Due to dose-dependent toxicity, high concentrations of DOX cannot be administered to cancer patients. Therefore, experiments have been directed towards revealing underlying mechanisms responsible for DOX resistance and ameliorating its adverse effects. Nuclear factor erythroid 2-related factor 2 (Nrf2) signaling is activated to increase levels of reactive oxygen species (ROS) in cells to protect them against oxidative stress. It has been reported that Nrf2 activation is associated with drug resistance. In cells exposed to DOX, stimulation of Nrf2 signaling protects cells against cell death. Various upstream mediators regulate Nrf2 in DOX resistance. Strategies, both pharmacological and genetic interventions, have been applied for reversing DOX resistance. However, Nrf2 induction is of importance for alleviating side effects of DOX. Pharmacological agents with naturally occurring compounds as the most common have been used for inducing Nrf2 signaling in DOX amelioration. Furthermore, signaling networks in which Nrf2 is a key player for protection against DOX adverse effects have been revealed and are discussed in the current review.</description><subject>Antioxidants</subject><subject>Apoptosis</subject><subject>Brain cancer</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>cancer therapy</subject><subject>Cell death</subject><subject>Chemoprotection</subject><subject>Chemoresistance</subject><subject>Chemotherapy</subject><subject>Doxorubicin</subject><subject>Drug dosages</subject><subject>Drug resistance</subject><subject>Experiments</subject><subject>Free radicals</subject><subject>Hypoxia</subject><subject>Inflammation</subject><subject>Kinases</subject><subject>Medical prognosis</subject><subject>nuclear factor erythroid 2-related factor 2 (Nrf2)</subject><subject>Oxidative stress</subject><subject>Proteins</subject><subject>Reactive oxygen species</subject><subject>redox signaling</subject><subject>Review</subject><subject>Side effects</subject><subject>Signal transduction</subject><subject>Toxicity</subject><issn>2076-3921</issn><issn>2076-3921</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkk1v1DAQhiMEolXplSOKxIXLFn875oBU7UKpVEHFx9lynHHWqyQOdtJ2_3293VJ18cWW55l3Zuy3KN5idEapQh_NMPlwhxGiiDL1ojgmSIoFVQS_fHY-Kk5T2qC8FKYVUq-LI0oFJ7JCx0X_PTpS_vLtYDo_tOW1mda3Zlv6oVyuoQ9jDBPYXGYozdCUq3AX4lx7m-M_Ifk0mcHCp_I6U7kZ05Xn49h5ax4yMrSKc1uufLLhBuL2TfHKmS7B6eN-Uvz5-uX38tvi6sfF5fL8amFZxaYFEyAa5yrsnOMSpG0sB-wsAsyIwkhBDUoKQSoriOVc1KS2ClvEkJGOI3pSXO51m2A2eoy-N3Grg_H64SLEVps4eduBFhKzRlIOu9JNrQxtXAUKY1KZiuKd1ue91jjXPTQ2zxlNdyB6GBn8WrfhRkulhOQ8C3x4FIjh7wxp0n1-D-g6M0CYkyZMCcI4Jiyj7_9DN2GO-WsyxQljuKoQztTZnrIxpBTBPTWDkd4ZQx8aIye8ez7CE_7PBvQeMHu2CA</recordid><startdate>20210226</startdate><enddate>20210226</enddate><creator>Mirzaei, Sepideh</creator><creator>Zarrabi, Ali</creator><creator>Hashemi, Farid</creator><creator>Zabolian, Amirhossein</creator><creator>Saleki, Hossein</creator><creator>Azami, Negar</creator><creator>Hamzehlou, Soodeh</creator><creator>Farahani, Mahdi Vasheghani</creator><creator>Hushmandi, Kiavash</creator><creator>Ashrafizadeh, Milad</creator><creator>Khan, Haroon</creator><creator>Kumar, Alan Prem</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QR</scope><scope>7T5</scope><scope>7TO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-0391-1769</orcidid><orcidid>https://orcid.org/0000-0002-3754-5712</orcidid><orcidid>https://orcid.org/0000-0001-6605-822X</orcidid><orcidid>https://orcid.org/0000-0001-9901-9534</orcidid></search><sort><creationdate>20210226</creationdate><title>Nrf2 Signaling Pathway in Chemoprotection and Doxorubicin Resistance: Potential Application in Drug Discovery</title><author>Mirzaei, Sepideh ; 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subjects | Antioxidants Apoptosis Brain cancer Cancer Cancer therapies cancer therapy Cell death Chemoprotection Chemoresistance Chemotherapy Doxorubicin Drug dosages Drug resistance Experiments Free radicals Hypoxia Inflammation Kinases Medical prognosis nuclear factor erythroid 2-related factor 2 (Nrf2) Oxidative stress Proteins Reactive oxygen species redox signaling Review Side effects Signal transduction Toxicity |
title | Nrf2 Signaling Pathway in Chemoprotection and Doxorubicin Resistance: Potential Application in Drug Discovery |
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