Multidrug Resistance in Cancer: Understanding Molecular Mechanisms, Immunoprevention and Therapeutic Approaches
Cancer is one of the leading causes of death worldwide. Several treatments are available for cancer treatment, but many treatment methods are ineffective against multidrug-resistant cancer. Multidrug resistance (MDR) represents a major obstacle to effective therapeutic interventions against cancer....
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| Vydáno v: | Frontiers in oncology Ročník 12; s. 891652 |
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| Hlavní autoři: | , , , , , , , , , , , , , , , |
| Médium: | Journal Article |
| Jazyk: | angličtina |
| Vydáno: |
Frontiers Media S.A
23.06.2022
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| Témata: | |
| ISSN: | 2234-943X, 2234-943X |
| On-line přístup: | Získat plný text |
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| Abstract | Cancer is one of the leading causes of death worldwide. Several treatments are available for cancer treatment, but many treatment methods are ineffective against multidrug-resistant cancer. Multidrug resistance (MDR) represents a major obstacle to effective therapeutic interventions against cancer. This review describes the known MDR mechanisms in cancer cells and discusses ongoing laboratory approaches and novel therapeutic strategies that aim to inhibit, circumvent, or reverse MDR development in various cancer types. In this review, we discuss both intrinsic and acquired drug resistance, in addition to highlighting hypoxia- and autophagy-mediated drug resistance mechanisms. Several factors, including individual genetic differences, such as mutations, altered epigenetics, enhanced drug efflux, cell death inhibition, and various other molecular and cellular mechanisms, are responsible for the development of resistance against anticancer agents. Drug resistance can also depend on cellular autophagic and hypoxic status. The expression of drug-resistant genes and the regulatory mechanisms that determine drug resistance are also discussed. Methods to circumvent MDR, including immunoprevention, the use of microparticles and nanomedicine might result in better strategies for fighting cancer. |
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| AbstractList | Cancer is one of the leading causes of death worldwide. Several treatments are available for cancer treatment, but many treatment methods are ineffective against multidrug-resistant cancer. Multidrug resistance (MDR) represents a major obstacle to effective therapeutic interventions against cancer. This review describes the known MDR mechanisms in cancer cells and discusses ongoing laboratory approaches and novel therapeutic strategies that aim to inhibit, circumvent, or reverse MDR development in various cancer types. In this review, we discuss both intrinsic and acquired drug resistance, in addition to highlighting hypoxia- and autophagy-mediated drug resistance mechanisms. Several factors, including individual genetic differences, such as mutations, altered epigenetics, enhanced drug efflux, cell death inhibition, and various other molecular and cellular mechanisms, are responsible for the development of resistance against anticancer agents. Drug resistance can also depend on cellular autophagic and hypoxic status. The expression of drug-resistant genes and the regulatory mechanisms that determine drug resistance are also discussed. Methods to circumvent MDR, including immunoprevention, the use of microparticles and nanomedicine might result in better strategies for fighting cancer. Cancer is one of the leading causes of death worldwide. Several treatments are available for cancer treatment, but many treatment methods are ineffective against multidrug-resistant cancer. Multidrug resistance (MDR) represents a major obstacle to effective therapeutic interventions against cancer. This review describes the known MDR mechanisms in cancer cells and discusses ongoing laboratory approaches and novel therapeutic strategies that aim to inhibit, circumvent, or reverse MDR development in various cancer types. In this review, we discuss both intrinsic and acquired drug resistance, in addition to highlighting hypoxia- and autophagy-mediated drug resistance mechanisms. Several factors, including individual genetic differences, such as mutations, altered epigenetics, enhanced drug efflux, cell death inhibition, and various other molecular and cellular mechanisms, are responsible for the development of resistance against anticancer agents. Drug resistance can also depend on cellular autophagic and hypoxic status. The expression of drug-resistant genes and the regulatory mechanisms that determine drug resistance are also discussed. Methods to circumvent MDR, including immunoprevention, the use of microparticles and nanomedicine might result in better strategies for fighting cancer.Cancer is one of the leading causes of death worldwide. Several treatments are available for cancer treatment, but many treatment methods are ineffective against multidrug-resistant cancer. Multidrug resistance (MDR) represents a major obstacle to effective therapeutic interventions against cancer. This review describes the known MDR mechanisms in cancer cells and discusses ongoing laboratory approaches and novel therapeutic strategies that aim to inhibit, circumvent, or reverse MDR development in various cancer types. In this review, we discuss both intrinsic and acquired drug resistance, in addition to highlighting hypoxia- and autophagy-mediated drug resistance mechanisms. Several factors, including individual genetic differences, such as mutations, altered epigenetics, enhanced drug efflux, cell death inhibition, and various other molecular and cellular mechanisms, are responsible for the development of resistance against anticancer agents. Drug resistance can also depend on cellular autophagic and hypoxic status. The expression of drug-resistant genes and the regulatory mechanisms that determine drug resistance are also discussed. Methods to circumvent MDR, including immunoprevention, the use of microparticles and nanomedicine might result in better strategies for fighting cancer. |
| Author | Nainu, Firzan Hassan, Mohammad Mahmudul Wahyudin, Elly Dhama, Kuldeep Rahman, Tanjilur Rahman, Nova Mahmud, Aar Rafi Emran, Talha Bin Abir, Mehedy Hasan Ahmed, Hossain Mitra, Saikat Shahriar, Asif Haque, Shafiul Siddiquee, Mohd. Faijanur - Rob Islam, Ariful Habiballah, Mahmoud M. |
| AuthorAffiliation | 9 Department of Biochemistry and Molecular Biology, Jahangirnagar University , Dhaka , Bangladesh 10 Department of Pharmacy, Faculty of Pharmacy, Hasanuddin University , Makassar , Indonesia 3 Department of Immunology and Microbiology, School of Medicine, University of Texas Rio Grande Valley , McAllen, TX , United States 7 Department of Biochemistry and Molecular Biology, University of Dhaka , Dhaka , Bangladesh 14 SMIRES for Consultation in Specialized Medical Laboratories, Jazan University , Jazan , Saudi Arabia 12 Division of Pathology, ICAR-Indian Veterinary Research Institute , Bareilly , India 15 Research and Scientific Studies Unit, College of Nursing and Allied Health Sciences, Jazan University , Jazan , Saudi Arabia 19 Department of Physiology, Biochemistry and Pharmacology, Faculty of Veterinary Medicine, Chattogram Veterinary and Animal Sciences University , Chattogram , Bangladesh 11 Department of Pharmacy, Faculty of Pharmacy, University of Dhaka , Dhaka , Bangladesh 18 Queensland |
| AuthorAffiliation_xml | – name: 5 Department of Biochemistry and Molecular Biology, Faculty of Biological Sciences, University of Chittagong , Chittagong , Bangladesh – name: 12 Division of Pathology, ICAR-Indian Veterinary Research Institute , Bareilly , India – name: 10 Department of Pharmacy, Faculty of Pharmacy, Hasanuddin University , Makassar , Indonesia – name: 15 Research and Scientific Studies Unit, College of Nursing and Allied Health Sciences, Jazan University , Jazan , Saudi Arabia – name: 9 Department of Biochemistry and Molecular Biology, Jahangirnagar University , Dhaka , Bangladesh – name: 4 Department of Biochemistry and Molecular Biology, Mawlana Bhashani Science and Technology University , Tangail , Bangladesh – name: 6 Faculty of Food Science and Technology, Chattogram Veterinary and Animal Sciences University , Chattogram , Bangladesh – name: 14 SMIRES for Consultation in Specialized Medical Laboratories, Jazan University , Jazan , Saudi Arabia – name: 2 Department of Pharmacy, Faculty of Allied Health Sciences, Daffodil International University , Dhaka , Bangladesh – name: 18 Queensland Alliance for One Health Sciences, School of Veterinary Science, The University of Queensland , Gatton, QLD , Australia – name: 7 Department of Biochemistry and Molecular Biology, University of Dhaka , Dhaka , Bangladesh – name: 17 EcoHealth Alliance , New York, NY , United States – name: 19 Department of Physiology, Biochemistry and Pharmacology, Faculty of Veterinary Medicine, Chattogram Veterinary and Animal Sciences University , Chattogram , Bangladesh – name: 1 Department of Pharmacy, BGC Trust University Bangladesh , Chittagong , Bangladesh – name: 11 Department of Pharmacy, Faculty of Pharmacy, University of Dhaka , Dhaka , Bangladesh – name: 13 Medical Laboratory Technology Department, Jazan University , Jazan , Saudi Arabia – name: 8 Department of Biotechnology and Genetic Engineering, University of Development Alternative , Dhaka , Bangladesh – name: 3 Department of Immunology and Microbiology, School of Medicine, University of Texas Rio Grande Valley , McAllen, TX , United States – name: 16 Bursa Uludağ University Faculty of Medicine , Bursa , Turkey |
| Author_xml | – sequence: 1 givenname: Talha Bin surname: Emran fullname: Emran, Talha Bin – sequence: 2 givenname: Asif surname: Shahriar fullname: Shahriar, Asif – sequence: 3 givenname: Aar Rafi surname: Mahmud fullname: Mahmud, Aar Rafi – sequence: 4 givenname: Tanjilur surname: Rahman fullname: Rahman, Tanjilur – sequence: 5 givenname: Mehedy Hasan surname: Abir fullname: Abir, Mehedy Hasan – sequence: 6 givenname: Mohd. Faijanur - Rob surname: Siddiquee fullname: Siddiquee, Mohd. Faijanur - Rob – sequence: 7 givenname: Hossain surname: Ahmed fullname: Ahmed, Hossain – sequence: 8 givenname: Nova surname: Rahman fullname: Rahman, Nova – sequence: 9 givenname: Firzan surname: Nainu fullname: Nainu, Firzan – sequence: 10 givenname: Elly surname: Wahyudin fullname: Wahyudin, Elly – sequence: 11 givenname: Saikat surname: Mitra fullname: Mitra, Saikat – sequence: 12 givenname: Kuldeep surname: Dhama fullname: Dhama, Kuldeep – sequence: 13 givenname: Mahmoud M. surname: Habiballah fullname: Habiballah, Mahmoud M. – sequence: 14 givenname: Shafiul surname: Haque fullname: Haque, Shafiul – sequence: 15 givenname: Ariful surname: Islam fullname: Islam, Ariful – sequence: 16 givenname: Mohammad Mahmudul surname: Hassan fullname: Hassan, Mohammad Mahmudul |
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| Copyright | Copyright © 2022 Emran, Shahriar, Mahmud, Rahman, Abir, Siddiquee, Ahmed, Rahman, Nainu, Wahyudin, Mitra, Dhama, Habiballah, Haque, Islam and Hassan. Copyright © 2022 Emran, Shahriar, Mahmud, Rahman, Abir, Siddiquee, Ahmed, Rahman, Nainu, Wahyudin, Mitra, Dhama, Habiballah, Haque, Islam and Hassan 2022 Emran, Shahriar, Mahmud, Rahman, Abir, Siddiquee, Ahmed, Rahman, Nainu, Wahyudin, Mitra, Dhama, Habiballah, Haque, Islam and Hassan |
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| Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 This article was submitted to Pharmacology of Anti-Cancer Drugs, a section of the journal Frontiers in Oncology Reviewed by: Hodaka Fujii, Hirosaki University, Japan; Ki Hyun Nam, Pohang University of Science and Technology, South Korea; Ana Podolski-Renic, Institute for Biological Research “Siniša Stanković” – National Institute of Republic of Serbia, Serbia Edited by: Milica Pešić, University of Belgrade, Serbia |
| OpenAccessLink | https://doaj.org/article/f892769914c74af7be4f6c343383b46a |
| PMID | 35814435 |
| PQID | 2688087162 |
| PQPubID | 23479 |
| ParticipantIDs | doaj_primary_oai_doaj_org_article_f892769914c74af7be4f6c343383b46a pubmedcentral_primary_oai_pubmedcentral_nih_gov_9262248 proquest_miscellaneous_2688087162 crossref_primary_10_3389_fonc_2022_891652 crossref_citationtrail_10_3389_fonc_2022_891652 |
| PublicationCentury | 2000 |
| PublicationDate | 2022-06-23 |
| PublicationDateYYYYMMDD | 2022-06-23 |
| PublicationDate_xml | – month: 06 year: 2022 text: 2022-06-23 day: 23 |
| PublicationDecade | 2020 |
| PublicationTitle | Frontiers in oncology |
| PublicationYear | 2022 |
| Publisher | Frontiers Media S.A |
| Publisher_xml | – name: Frontiers Media S.A |
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