d-a-Tocopheryl Polyethylene Glycol 1000 Succinate and a small-molecule Survivin suppressant synergistically induce apoptosis in SKBR3 breast cancer cells
Autor: | Gregoria Gregoriou, Christiana M. Neophytou, Avgoustinos Mesaritis, Andreas I. Constantinou |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Survivin lcsh:Medicine Drug development Apoptosis Breast Neoplasms Article 03 medical and health sciences Breast cancer Drug Delivery Systems 0302 clinical medicine medicine Humans Vitamin E lcsh:Science PI3K/AKT/mTOR pathway Multidisciplinary Chemistry lcsh:R Imidazoles Drug Synergism medicine.disease Gene Expression Regulation Neoplastic 030104 developmental biology Mechanism of action SKBR3 030220 oncology & carcinogenesis Drug delivery MCF-7 Cells Cancer research Female lcsh:Q medicine.symptom Immortalised cell line Naphthoquinones |
Zdroj: | Scientific Reports, Vol 9, Iss 1, Pp 1-10 (2019) Scientific Reports |
ISSN: | 2045-2322 |
Popis: | Breast cancer is the second in mortality rate malignancy among women. Despite the many advances in breast cancer treatment, there is still a need to improve drug efficacy and reduce non-specific effects. D-alpha-tocopheryl polyethylene glycol succinate (TPGS) is frequently used in the development of drug delivery systems to improve the pharmacokinetics of anti-cancer drugs and reduce multi-drug resistance. We have previously shown that TPGS not only acts as a carrier molecule but also exerts anti-cancer effects. As part of this study, we investigated the effect of TPGS with YM155, a small molecule suppressant of Survivin, in various breast cancer cell lines representing different subtypes of the disease. We aimed to evaluate the presumed synergistic effect of the TPGS-YM155 combination and reveal its mechanism of action. Our results show that the TPGS-YM155 combination acts synergistically to reduce specifically the viability of SKBR3 cells. The combination of these agents reduced activation of the AKT pathway, decreased Survivin and Bcl-2 levels, and induced caspase-dependent and independent apoptosis via the mitochondrial pathway. Importantly, the TPGS-YM155 combination did not significantly affect the viability of MCF-10A normal immortalized cells. In conclusion, the combination of YM155 and TPGS could be a promising approach against SKBR3-type breast cancer. |
Databáze: | OpenAIRE |
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