Breast Cancer Subtypes Present a Differential Production of Reactive Oxygen Species (ROS) and Susceptibility to Antioxidant Treatment

Due to their crucial role in cell metabolism and homeostasis, alterations in mitochondrial biology and function have been related to the progression of diverse diseases including cancer. One of the consequences associated to mitochondrial dysfunction is the production of reactive oxygen species (ROS...

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Main Authors: Fabiola Lilí Sarmiento-Salinas, Alam Delgado-Magallón, José Benito Montes-Alvarado, Dalia Ramírez-Ramírez, Juan Carlos Flores-Alonso, Paulina Cortés-Hernández, Julio Reyes-Leyva, Irma Herrera-Camacho, Maricruz Anaya-Ruiz, Rosana Pelayo, Lourdes Millán-Pérez-Peña, Paola Maycotte
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-06-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fonc.2019.00480/full
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author Fabiola Lilí Sarmiento-Salinas
Fabiola Lilí Sarmiento-Salinas
Alam Delgado-Magallón
Alam Delgado-Magallón
José Benito Montes-Alvarado
Dalia Ramírez-Ramírez
Juan Carlos Flores-Alonso
Paulina Cortés-Hernández
Julio Reyes-Leyva
Irma Herrera-Camacho
Maricruz Anaya-Ruiz
Rosana Pelayo
Lourdes Millán-Pérez-Peña
Paola Maycotte
author_facet Fabiola Lilí Sarmiento-Salinas
Fabiola Lilí Sarmiento-Salinas
Alam Delgado-Magallón
Alam Delgado-Magallón
José Benito Montes-Alvarado
Dalia Ramírez-Ramírez
Juan Carlos Flores-Alonso
Paulina Cortés-Hernández
Julio Reyes-Leyva
Irma Herrera-Camacho
Maricruz Anaya-Ruiz
Rosana Pelayo
Lourdes Millán-Pérez-Peña
Paola Maycotte
author_sort Fabiola Lilí Sarmiento-Salinas
collection DOAJ
description Due to their crucial role in cell metabolism and homeostasis, alterations in mitochondrial biology and function have been related to the progression of diverse diseases including cancer. One of the consequences associated to mitochondrial dysfunction is the production of reactive oxygen species (ROS). ROS are known to have a controversial role during cancer initiation and progression and although several studies have tried to manipulate intracellular ROS levels using antioxidants or pro-oxidation conditions, it is not yet clear how to target oxidation for cancer therapy. In this study, we found differences in mitochondrial morphology in breast cancer cells when compared to a non-tumorigenic cell line and differences in mitochondrial function among breast cancer subtypes when exploring gene-expression data from the TCGA tumor dataset. Interestingly, we found increased ROS levels in triple negative breast cancer (TNBC) cell lines and a dependency on ROS for survival since antioxidant treatment induced cell death in TNBC cells but not in an estrogen receptor positive (ER+) cell line. Moreover, we identified the mitochondria as the main source of ROS in TNBC cell lines. Our results indicate a potential use for ROS as a target for therapy in the TNBC subtype which currently has the worst prognosis among all breast cancers and remains as the only breast cancer subtype which lacks a targeted therapy.
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spelling doaj.art-d288283853f4474fb89bcfd359ccfbcf2022-12-22T03:53:12ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2019-06-01910.3389/fonc.2019.00480463964Breast Cancer Subtypes Present a Differential Production of Reactive Oxygen Species (ROS) and Susceptibility to Antioxidant TreatmentFabiola Lilí Sarmiento-Salinas0Fabiola Lilí Sarmiento-Salinas1Alam Delgado-Magallón2Alam Delgado-Magallón3José Benito Montes-Alvarado4Dalia Ramírez-Ramírez5Juan Carlos Flores-Alonso6Paulina Cortés-Hernández7Julio Reyes-Leyva8Irma Herrera-Camacho9Maricruz Anaya-Ruiz10Rosana Pelayo11Lourdes Millán-Pérez-Peña12Paola Maycotte13Centro de Investigación Biomédica de Oriente, Instituto Mexicano del Seguro Social, Puebla, MexicoPosgrado en Ciencias Químicas, Benemérita Universidad Autónoma de Puebla, Puebla, MexicoCentro de Investigación Biomédica de Oriente, Instituto Mexicano del Seguro Social, Puebla, MexicoDepartamento de Bioquímica, Instituto Tecnológico de Acapulco, Acapulco de Juárez, MexicoCentro de Investigación Biomédica de Oriente, Instituto Mexicano del Seguro Social, Puebla, MexicoCentro de Investigación Biomédica de Oriente, Instituto Mexicano del Seguro Social, Puebla, MexicoCentro de Investigación Biomédica de Oriente, Instituto Mexicano del Seguro Social, Puebla, MexicoCentro de Investigación Biomédica de Oriente, Instituto Mexicano del Seguro Social, Puebla, MexicoCentro de Investigación Biomédica de Oriente, Instituto Mexicano del Seguro Social, Puebla, MexicoCentro de Química, Instituto de Ciencias, Benemérita Universidad Autónoma de Puebla, Puebla, MexicoCentro de Investigación Biomédica de Oriente, Instituto Mexicano del Seguro Social, Puebla, MexicoCentro de Investigación Biomédica de Oriente, Instituto Mexicano del Seguro Social, Puebla, MexicoCentro de Química, Instituto de Ciencias, Benemérita Universidad Autónoma de Puebla, Puebla, MexicoCONACYT-Centro de Investigación Biomédica de Oriente, Instituto Mexicano del Seguro Social, Puebla, MexicoDue to their crucial role in cell metabolism and homeostasis, alterations in mitochondrial biology and function have been related to the progression of diverse diseases including cancer. One of the consequences associated to mitochondrial dysfunction is the production of reactive oxygen species (ROS). ROS are known to have a controversial role during cancer initiation and progression and although several studies have tried to manipulate intracellular ROS levels using antioxidants or pro-oxidation conditions, it is not yet clear how to target oxidation for cancer therapy. In this study, we found differences in mitochondrial morphology in breast cancer cells when compared to a non-tumorigenic cell line and differences in mitochondrial function among breast cancer subtypes when exploring gene-expression data from the TCGA tumor dataset. Interestingly, we found increased ROS levels in triple negative breast cancer (TNBC) cell lines and a dependency on ROS for survival since antioxidant treatment induced cell death in TNBC cells but not in an estrogen receptor positive (ER+) cell line. Moreover, we identified the mitochondria as the main source of ROS in TNBC cell lines. Our results indicate a potential use for ROS as a target for therapy in the TNBC subtype which currently has the worst prognosis among all breast cancers and remains as the only breast cancer subtype which lacks a targeted therapy.https://www.frontiersin.org/article/10.3389/fonc.2019.00480/fullbreast cancerROSmitochondriamitochondrial morphologymitochondrial ROS
spellingShingle Fabiola Lilí Sarmiento-Salinas
Fabiola Lilí Sarmiento-Salinas
Alam Delgado-Magallón
Alam Delgado-Magallón
José Benito Montes-Alvarado
Dalia Ramírez-Ramírez
Juan Carlos Flores-Alonso
Paulina Cortés-Hernández
Julio Reyes-Leyva
Irma Herrera-Camacho
Maricruz Anaya-Ruiz
Rosana Pelayo
Lourdes Millán-Pérez-Peña
Paola Maycotte
Breast Cancer Subtypes Present a Differential Production of Reactive Oxygen Species (ROS) and Susceptibility to Antioxidant Treatment
Frontiers in Oncology
breast cancer
ROS
mitochondria
mitochondrial morphology
mitochondrial ROS
title Breast Cancer Subtypes Present a Differential Production of Reactive Oxygen Species (ROS) and Susceptibility to Antioxidant Treatment
title_full Breast Cancer Subtypes Present a Differential Production of Reactive Oxygen Species (ROS) and Susceptibility to Antioxidant Treatment
title_fullStr Breast Cancer Subtypes Present a Differential Production of Reactive Oxygen Species (ROS) and Susceptibility to Antioxidant Treatment
title_full_unstemmed Breast Cancer Subtypes Present a Differential Production of Reactive Oxygen Species (ROS) and Susceptibility to Antioxidant Treatment
title_short Breast Cancer Subtypes Present a Differential Production of Reactive Oxygen Species (ROS) and Susceptibility to Antioxidant Treatment
title_sort breast cancer subtypes present a differential production of reactive oxygen species ros and susceptibility to antioxidant treatment
topic breast cancer
ROS
mitochondria
mitochondrial morphology
mitochondrial ROS
url https://www.frontiersin.org/article/10.3389/fonc.2019.00480/full
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