Abstract
Triple-negative breast cancer (TNBC) is an aggressive breast cancer subtype that promotes a higher risk of metastasis and cancer reoccurrence. Cisplatin is one of the potential anticancer drugs for treating TNBC. However, the occurrence of cisplatin resistance still remains one of the challenges in fully eradicating TNBC. The presence of cancer stem cells (CSCs) has been proposed as one of the factors contributing to the development of cisplatin resistance. In this study, we aimed to characterize the cellular properties and reveal the corresponding putative target genes involved in cisplatin resistance associated with CSCs using the TNBC cell line (MDA-MB-231). CSC-like cells were isolated from parental cells and the therapeutic effect of cisplatin on CSC-like cells was compared to that of the parental cells via cell characterization bioassays. A PCR array was then conducted to study the expression of cellular mRNA for each subpopulation. As compared to treated parental cells, treated CSCs displayed lower events of late apoptosis/necrosis and G2/M phase cell arrest, with higher mammosphere formation capacity. Furthermore, a distinct set of putative target genes correlated to the Hedgehog pathway and angiogenesis were dysregulated solely in CSC-like cells after cisplatin treatment, which were closely related to the regulation of chemoresistance and self-renewability in breast cancer. In summary, both cellular and gene expression studies suggest the attenuated cytotoxicity of cisplatin in CSC-like cells as compared to parental cells. Understanding the role of dysregulated putative target genes induced by cisplatin in CSCs may aid in the potential development of therapeutic targets for cisplatin-resistant breast cancer.
Highlights
Triple-negative breast cancer (TNBC) is a breast cancer subtype defined by its lack of an estrogen receptor (ER) and progesterone receptor (PR), and the absence of amplification of human epidermal growth factor receptors 2 (HER-2) [1]
The present study described the effect of cisplatin on cancer stem cells (CSCs)-like subpopulations in comparison to its parental cells in the TNBC cell line, MDA-MB-231
The findings of this study suggest the higher tolerance of sorted CSC-like cells from
Summary
Triple-negative breast cancer (TNBC) is a breast cancer subtype defined by its lack of an estrogen receptor (ER) and progesterone receptor (PR), and the absence of amplification of human epidermal growth factor receptors 2 (HER-2) [1]. TNBC accounts for approximately 10–24% of all breast cancer cases, and is more common in Asian countries [2]. In Malaysia, the incidence of TNBC has been reported to range from 12.3% to 17.6% of the total breast cancer cases [3,4,5]. TNBC displays more aggressive behavior than other breast cancer subtypes, and is strongly associated with the recurrence of metastatic breast cancer, and metastasis is a major cause of patient morbidity and mortality [6,7].
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