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Counteracting Chemoresistance with Metformin in Breast Cancers: Targeting Cancer Stem Cells

Despite the leaps and bounds in achieving success in the management and treatment of breast cancers through surgery, chemotherapy, and radiotherapy, breast cancer remains the most frequently occurring cancer in women and the most common cause of cancer-related deaths among women. Systemic therapeuti...

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Autores principales: Samuel, Samson Mathews, Varghese, Elizabeth, Koklesová, Lenka, Líšková, Alena, Kubatka, Peter, Büsselberg, Dietrich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565921/
https://www.ncbi.nlm.nih.gov/pubmed/32883003
http://dx.doi.org/10.3390/cancers12092482
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author Samuel, Samson Mathews
Varghese, Elizabeth
Koklesová, Lenka
Líšková, Alena
Kubatka, Peter
Büsselberg, Dietrich
author_facet Samuel, Samson Mathews
Varghese, Elizabeth
Koklesová, Lenka
Líšková, Alena
Kubatka, Peter
Büsselberg, Dietrich
author_sort Samuel, Samson Mathews
collection PubMed
description Despite the leaps and bounds in achieving success in the management and treatment of breast cancers through surgery, chemotherapy, and radiotherapy, breast cancer remains the most frequently occurring cancer in women and the most common cause of cancer-related deaths among women. Systemic therapeutic approaches, such as chemotherapy, although beneficial in treating and curing breast cancer subjects with localized breast tumors, tend to fail in metastatic cases of the disease due to (a) an acquired resistance to the chemotherapeutic drug and (b) the development of intrinsic resistance to therapy. The existence of cancer stem cells (CSCs) plays a crucial role in both acquired and intrinsic chemoresistance. CSCs are less abundant than terminally differentiated cancer cells and confer chemoresistance through a unique altered metabolism and capability to evade the immune response system. Furthermore, CSCs possess active DNA repair systems, transporters that support multidrug resistance (MDR), advanced detoxification processes, and the ability to self-renew and differentiate into tumor progenitor cells, thereby supporting cancer invasion, metastasis, and recurrence/relapse. Hence, current research is focusing on targeting CSCs to overcome resistance and improve the efficacy of the treatment and management of breast cancer. Studies revealed that metformin (1, 1-dimethylbiguanide), a widely used anti-hyperglycemic agent, sensitizes tumor response to various chemotherapeutic drugs. Metformin selectively targets CSCs and improves the hypoxic microenvironment, suppresses the tumor metastasis and inflammation, as well as regulates the metabolic programming, induces apoptosis, and reverses epithelial–mesenchymal transition and MDR. Here, we discuss cancer (breast cancer) and chemoresistance, the molecular mechanisms of chemoresistance in breast cancers, and metformin as a chemo-sensitizing/re-sensitizing agent, with a particular focus on breast CSCs as a critical contributing factor to acquired and intrinsic chemoresistance. The review outlines the prospects and directions for a better understanding and re-purposing of metformin as an anti-cancer/chemo-sensitizing drug in the treatment of breast cancer. It intends to provide a rationale for the use of metformin as a combinatory therapy in a clinical setting.
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spelling pubmed-75659212020-10-26 Counteracting Chemoresistance with Metformin in Breast Cancers: Targeting Cancer Stem Cells Samuel, Samson Mathews Varghese, Elizabeth Koklesová, Lenka Líšková, Alena Kubatka, Peter Büsselberg, Dietrich Cancers (Basel) Review Despite the leaps and bounds in achieving success in the management and treatment of breast cancers through surgery, chemotherapy, and radiotherapy, breast cancer remains the most frequently occurring cancer in women and the most common cause of cancer-related deaths among women. Systemic therapeutic approaches, such as chemotherapy, although beneficial in treating and curing breast cancer subjects with localized breast tumors, tend to fail in metastatic cases of the disease due to (a) an acquired resistance to the chemotherapeutic drug and (b) the development of intrinsic resistance to therapy. The existence of cancer stem cells (CSCs) plays a crucial role in both acquired and intrinsic chemoresistance. CSCs are less abundant than terminally differentiated cancer cells and confer chemoresistance through a unique altered metabolism and capability to evade the immune response system. Furthermore, CSCs possess active DNA repair systems, transporters that support multidrug resistance (MDR), advanced detoxification processes, and the ability to self-renew and differentiate into tumor progenitor cells, thereby supporting cancer invasion, metastasis, and recurrence/relapse. Hence, current research is focusing on targeting CSCs to overcome resistance and improve the efficacy of the treatment and management of breast cancer. Studies revealed that metformin (1, 1-dimethylbiguanide), a widely used anti-hyperglycemic agent, sensitizes tumor response to various chemotherapeutic drugs. Metformin selectively targets CSCs and improves the hypoxic microenvironment, suppresses the tumor metastasis and inflammation, as well as regulates the metabolic programming, induces apoptosis, and reverses epithelial–mesenchymal transition and MDR. Here, we discuss cancer (breast cancer) and chemoresistance, the molecular mechanisms of chemoresistance in breast cancers, and metformin as a chemo-sensitizing/re-sensitizing agent, with a particular focus on breast CSCs as a critical contributing factor to acquired and intrinsic chemoresistance. The review outlines the prospects and directions for a better understanding and re-purposing of metformin as an anti-cancer/chemo-sensitizing drug in the treatment of breast cancer. It intends to provide a rationale for the use of metformin as a combinatory therapy in a clinical setting. MDPI 2020-09-01 /pmc/articles/PMC7565921/ /pubmed/32883003 http://dx.doi.org/10.3390/cancers12092482 Text en © 2020 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/).
spellingShingle Review
Samuel, Samson Mathews
Varghese, Elizabeth
Koklesová, Lenka
Líšková, Alena
Kubatka, Peter
Büsselberg, Dietrich
Counteracting Chemoresistance with Metformin in Breast Cancers: Targeting Cancer Stem Cells
title Counteracting Chemoresistance with Metformin in Breast Cancers: Targeting Cancer Stem Cells
title_full Counteracting Chemoresistance with Metformin in Breast Cancers: Targeting Cancer Stem Cells
title_fullStr Counteracting Chemoresistance with Metformin in Breast Cancers: Targeting Cancer Stem Cells
title_full_unstemmed Counteracting Chemoresistance with Metformin in Breast Cancers: Targeting Cancer Stem Cells
title_short Counteracting Chemoresistance with Metformin in Breast Cancers: Targeting Cancer Stem Cells
title_sort counteracting chemoresistance with metformin in breast cancers: targeting cancer stem cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565921/
https://www.ncbi.nlm.nih.gov/pubmed/32883003
http://dx.doi.org/10.3390/cancers12092482
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