Title:Effects of Epirubicin and Cisplatin Against 4T1 Breast Cancer Cells are Enhanced by Myrtucommulone-A
Volume: 17
Issue: 3
Author(s): Kenan Izgi, Banu Iskender, Cagri Sakalar, Aslihan Arslanhan, Esra Hilal Yuksek, Esra Hizar and Halit Canatan
Affiliation:
Keywords:
Myrtucommulone A, Cancer, Cisplatin, Epirubicin, 4T1, Cancer resistance.
Abstract: Background: The number of cancer cases around the world has increased according to the World Health
Organization (WHO) reports, nearly 14 million new cases and 8.2 million cancer associated mortalities have been
reported in 2012. Chemotherapeutic resistance is a major problematic issue in the management of patients with breast
tumor.
Objective: In this study, the apoptotic gene profile of 4T1 mouse breast cancer cells treated with MC-A in combination
with cisplatin or epirubicin was evaluated to decipher the possible apoptotic molecular targets.
Methods: The effects of MC-A in combination with cisplatin (CIS) or epirubicin (EPI) on cytotoxicity, cell migration,
wound healing, clonogenicity along with enhanced effect of these combinations on 84 apoptosis related genes were
tested in 4T1 cancer cells.
Results: MC-A in combination with epirubicin or cisplatin robustly induced cytotoxicity in 4T1 cells in vitro. MC-A in
combination with cisplatin or epirubicin showed significantly inhibition of cell migration compared to treatment with
each agent alone. Genes involved in positive regulation of apoptosis, negative regulator of apoptosis, death-like,
mitochondrial apoptotic signaling, induction of apoptosis through DR3 and DR4/5 death receptors, and anti-apoptosis
were highly affected in MC-A+cisplatin or MC-A+epirubicin combinations compared to each agent only.
Conclusions: In conclusion, the apoptotic response of 4T1 cancer cells to chemotherapeutic drugs occurs in different
ways. MC-A in combination with these chemotherapeutic drugs could modulate the expression of genes involved in
both extrinsic and intrinsic pathways of apoptosis, leading to higly effective apoptotic signalling in cancer treatment.
