MSc.Thesis Defense:Eda Kapan
ANTIBIOTIC-BASED STRATEGIES TO OVERCOME DRUG RESISTANCE IN CANCER CELLS THROUGH OXPHOS
Eda Kapan
Molecular Biology, Genetics and Bioengineering,
MSc. Thesis, 2024
Thesis Jury
Asst.Prof. Alex Lyakhovich (Thesis Advisor)
Prof. Levent Öztürk
Assoc.Prof. Ceren Çıracı Muğan
Date & Time: 18th, 2024 – 12.40 PM
Place: FASS G048
Keywords : Cancer chemoresistance, Oxidative phosphorylation,
Triple-negative breast cancer, Mitochondrial dysfunction, Antibiotic repurposing, Targeted therapy
.
Abstract
Chemoresistance represents a significant barrier to effective treatment outcomes in TNBC, making it one of the most difficult subtypes of breast cancer to treat. Conducting in vitro and in vivo experiments, this study investigated the effectiveness of antibiotics and TPP-conjugated derivatives in inhibiting OXPHOS using cyclophosphamide-resistant MDA-MB-468 TNBC cells and their parental counterparts. The results showed that resistant cells were more sensitive to AMX and FSS, had higher ATP levels, improved mitochondrial function, and higher oxygen consumption. Particularly in resistant cells, AMX treatment successfully reduced MMP-9 and MMP-2 activities as well as the stemness markers Sox-2 and Nanog. TPP-linked antibiotics showed improved efficacy against resistant cells, suggesting effective mitochondrial targeting. Furthermore, the upregulation of mitochondrial complex II activity reveals its potential role in the development of chemotherapy resistance. Also, combinatorial therapy demonstrated a synergistic effect of cyclophosphamide and AMX in combating resistant cells. Although AMX had little effect on the parent tumors, it dramatically reduced tumor growth in resistant TNBC xenografts, according to in vivo studies. In conclusion, antibiotics and their TPP-conjugated derivatives appear to be promising therapeutic approaches to treating chemoresistant TNBC by targeting OXPHOS through various mechanisms including impairing mitochondrial function, reducing the properties of stemness, and preventing metastasis