TNBC Therapeutics Based on Combination of Fusarochromanone with EGFR Inhibitors

• Published in: Biomedicines Vol. 10; no. 11; p. 2906
• Main Authors: Carroll, Natalie, Youngblood, Reneau, Smith, Alena, Dragoi, Ana-Maria, Salvatore, Brian A, Mahdavian, Elahe
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.11.2022; MDPI
• Subjects: Antimitotic agents; Antineoplastic agents; Antitumor activity; Breast cancer; Cancer therapies; Cell proliferation; Cell viability; Chemotherapy; Clinical outcomes; Drug development; Drug resistance; Drug therapy, Combination; EGFR; Epidermal growth factor receptors; erlotinib; everolimus; FDA approval; fusarochromanone; Genomes; Kinases; Metastasis; Methods; mTOR; Mycotoxins; Oncology; Phosphorylation; Protein synthesis; Proteins; Signal transduction; Targeted cancer therapy; TNBC; TOR protein; United States; everolimus; fusarochromanone; erlotinib; lapatinib; mTOR; phenotypic screens; synergistic; TNBC; EGFR; drug combinations
• ISSN: 2227-9059; 2227-9059
• DOI: 10.3390/biomedicines10112906

Fusarochromanone is an experimental drug with unique and potent anti-cancer activity. Current cancer therapies often incorporate a combination of drugs to increase efficacy and decrease the development of drug resistance. In this study, we used drug combinations and cellular phenotypic screens to address important questions about FC101's mode of action and its potential therapeutic synergies in triple negative breast cancer (TNBC). We hypothesized that FC101's activity against TNBC is similar to the mTOR inhibitor, everolimus, because FC101 downregulates the phosphorylation of two mTOR substrates, S6K and S6. Since everolimus synergistically enhances the anti-cancer activities of two known EGFR inhibitors (erlotinib or lapatinib) in TNBC, we performed analogous studies with FC101. Phenotypic cellular assays helped assess whether FC101 acts similarly to everolimus, in both single and combination treatments with the two inhibitors. FC101 outperformed all other single treatments in both cell proliferation and viability assays. However, unlike everolimus, FC101 produced a sustained decrease in cell viability in drug washout studies. None of the other drugs were able to maintain comparable effects upon removal. Although we observed slightly additive effects when the TNBC cells were treated with FC101 and the two EGFR inhibitors, those effects were not truly synergistic in the manner displayed with everolimus.