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A gold-based inhibitor of oxidative phosphorylation is effective against triple negative breast cancer.
Mertens, R Tyler; Kim, Jong Hyun; Ofori, Samuel; Olelewe, Chibuzor; Kamitsuka, Paul J; Kwakye, Gunnar F; Awuah, Samuel G.
Affiliation
  • Mertens RT; Department of Chemistry, University of Kentucky; Lexington, KY 40506, United States.
  • Kim JH; Department of Chemistry, University of Kentucky; Lexington, KY 40506, United States.
  • Ofori S; Department of Chemistry, University of Kentucky; Lexington, KY 40506, United States; Department of Neuroscience, Oberlin College, Oberlin, OH 44074, United States; Department of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, Lexington, KY 40536, United States; University of Ke
  • Olelewe C; Department of Chemistry, University of Kentucky; Lexington, KY 40506, United States; Department of Neuroscience, Oberlin College, Oberlin, OH 44074, United States; Department of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, Lexington, KY 40536, United States; University of Ke
  • Kamitsuka PJ; Department of Neuroscience, Oberlin College, Oberlin, OH 44074, United States.
  • Kwakye GF; Department of Neuroscience, Oberlin College, Oberlin, OH 44074, United States.
  • Awuah SG; Department of Chemistry, University of Kentucky; Lexington, KY 40506, United States; Department of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, Lexington, KY 40536, United States; University of Kentucky Markey Cancer Center, USA. Electronic address: awuah@uky.edu.
Biomed Pharmacother ; 170: 116010, 2024 Jan.
Article in En | MEDLINE | ID: mdl-38128183
ABSTRACT
Triple-negative breast cancer (TNBC) is associated with metabolic heterogeneity and poor prognosis with limited treatment options. New treatment paradigms for TNBC remains an unmet need. Thus, therapeutics that target metabolism are particularly attractive approaches. We previously designed organometallic Au(III) compounds capable of modulating mitochondrial respiration by ligand tuning with high anticancer potency in vitro and in vivo. Here, we show that an efficacious Au(III) dithiocarbamate (AuDTC) compound induce mitochondrial dysfunction and oxidative damage in cancer cells. Efficacy of AuDTC in TNBC mouse models harboring mitochondrial oxidative phosphorylation (OXPHOS) dependence and metabolic heterogeneity establishes its therapeutic potential following systemic delivery. This provides evidence that AuDTC is an effective modulator of mitochondrial respiration worthy of clinical development in the context of TNBC. ONE SENTENCE

SUMMARY:

Metabolic-targeting of triple-negative breast cancer by gold anticancer agent may provide efficacious therapy.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Triple Negative Breast Neoplasms / Antineoplastic Agents Limits: Animals / Humans Language: En Journal: Biomed Pharmacother Year: 2024 Document type: Article Affiliation country: United States Country of publication: France

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Triple Negative Breast Neoplasms / Antineoplastic Agents Limits: Animals / Humans Language: En Journal: Biomed Pharmacother Year: 2024 Document type: Article Affiliation country: United States Country of publication: France