In vitro cytotoxic effect of PARP inhibitor alone and in combination with nab-paclitaxel on triple-negative and luminal A breast cancer cells

被引:7
|
作者
Topcul, Mehmet [1 ]
Cetin, Idil [1 ]
Turan, Suna Ozbas [2 ]
Ozar, Melek Ozlem Kolusayin [3 ]
机构
[1] Istanbul Univ, Dept Biol, Fac Sci, TR-34459 Istanbul, Turkey
[2] Marmara Univ, Fac Pharm, TR-34668 Istanbul, Turkey
[3] Istanbul Univ, Cerrahpasa Med Fac, Dept Forens Sci, TR-34098 Istanbul, Turkey
关键词
poly(ADP-ribose) polymerase inhibitor; nab-paclitaxel; MCF-7; MDA-MB-231; xCELLigence Real-Time Cell Analysis DP instrument; CHEMOTHERAPY; SUBTYPES; CHEMOSENSITIVITY; MICROTUBULES; GEMCITABINE; FORMULATION; PROGNOSIS; CISPLATIN; TARGETS; ALBUMIN;
D O I
10.3892/or.2018.6364
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In the present study, the in vitro cytotoxic effect of poly(ADP-ribose) polymerase (PARP) inhibitor alone and in combination with nab-paclitaxel was evaluated on human triple-negative breast cancer (TNBC) cell line MDA-MB-231 and human luminal A breast cancer cell line MCF-7. For this purpose, cell index (CI) values obtained from xCELLigence Real-Time Cell Analysis (RTCA) DP instrument, mitotic index (MI), labelling index (LI) and apoptotic index (AI) analysis among cell kinetic parameters were used. As a result of PARP inhibitor application, there was a significant decrease in CI, MI and LI and a significant increase in AI for all the experimental groups. After application of PARP inhibitor in combination with nab-paclitaxel, the CI values were decreased for both cell lines, and the differences between the control and all the experimental groups were statistically significant (P<0.01) for all applications. PARP inhibitor, alone or in combination with nab-paclitaxel offers a promising treatment modality in different breast cancer subtypes.
引用
收藏
页码:527 / 535
页数:9
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