Ergosterol Peroxide Disrupts Triple-Negative Breast Cancer Mitochondrial Function and Inhibits Tumor Growth and Metastasis

Ergosterol peroxide (EP) triggers apoptosis pathways by inducing reactive oxygen species (ROS) in TNBC cell lines. Excess ROS production is associated with major damage to mitochondria. We hypothesized that EP may act through ROS-induced mitochondrial dysfunction. Therefore, we performed a series of assays that assessed mitochondrial membrane potential (MMP), cellular respiration, and glycolysis in TNBC models. Cardiomyocytes derived from human-induced pluripotent stem cells were chosen as a non-cancerous model because of their high mitochondrial content. Two in vivo TNBC models were used to quantify the effect of EP on tumor volume and metastases. EP reduced MMP and disrupted mitochondrial functions exclusively in TNBC cells. In vivo EP was effective in reducing tumor volume without affecting liver function. There was also a significant decrease in metastasis to the lung, liver, and cancer stem cells following treatment. These results suggest EP is a promising therapy for TNBC.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2025-05-10
DOI
https://doi.org/10.3390/ijms26104588
Citations
2
Primary Topic
Mitochondrial Function and Pathology
Type
article
Field-Weighted Citation Impact
1.61
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article

Ergosterol Peroxide Disrupts Triple-Negative Breast Cancer Mitochondrial Function and Inhibits Tumor Growth and Metastasis

Sona Rivas‐Tumanyan, Israel Almodóvar‐Rivera, Naydi Pérez-Ríos, Fatima Rivas et al.
2 citations
International Journal of Molecular Sciences
Mitochondrial Function and Pathology
1.61
article

Ergosterol Peroxide Disrupts Triple-Negative Breast Cancer Mitochondrial Function and Inhibits Tumor Growth and Metastasis

Sona Rivas‐Tumanyan, Israel Almodóvar‐Rivera, Naydi Pérez-Ríos, Fatima Rivas, Michelle Martínez, Maribella Domenech, Natalia Espinosa-Ponce, Luz V. Arroyo-Cruz, Taotao Ling, Carlos Barreto-Gamarra, Aliyah L. Bocachica-Adorno, Adriana Y. Aponte-Ramos, Paola S. Rivera-Fuentes
article en
2 citations

Abstract

Ergosterol peroxide (EP) triggers apoptosis pathways by inducing reactive oxygen species (ROS) in TNBC cell lines. Excess ROS production is associated with major damage to mitochondria. We hypothesized that EP may act through ROS-induced mitochondrial dysfunction. Therefore, we performed a series of assays that assessed mitochondrial membrane potential (MMP), cellular respiration, and glycolysis in TNBC models. Cardiomyocytes derived from human-induced pluripotent stem cells were chosen as a non-cancerous model because of their high mitochondrial content. Two in vivo TNBC models were used to quantify the effect of EP on tumor volume and metastases. EP reduced MMP and disrupted mitochondrial functions exclusively in TNBC cells. In vivo EP was effective in reducing tumor volume without affecting liver function. There was also a significant decrease in metastasis to the lung, liver, and cancer stem cells following treatment. These results suggest EP is a promising therapy for TNBC.

International Journal of Molecular SciencesVol. 26(10)
Louisiana State University (US), University of Puerto Rico, Medical Sciences Campus (PR), University of Puerto Rico at Río Piedras (PR), InterAmerican University of Puerto Rico (PR), University of Puerto Rico System (PR), Central University of the Caribbean (PR), University of Puerto Rico at Bayamón (PR), University of Puerto Rico-Mayaguez (PR)
Good health and well-being
Openalex Percentile: Top 17%
Mitochondrial Function and Pathology
1.61
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