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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.
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页码:527 / 535
页数:9
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