| نویسندگان | الهه سید حسینی,مرضیه علیزاده زایری,صادق باباشاه,روح اله نخعی سیستانی,مجید صادقی زاده,حامد حداد کاشانی,جواد امینی مهابادی,فاطمه ایزدپناه,محمدعلی اطلسی,حسین نیکزاد |
| نشریه | CELL BIOL TOXICOL |
| شماره صفحات | 1 |
| شماره مجلد | 33 |
| ضریب تاثیر (IF) | 3.39 |
| نوع مقاله | Full Paper |
| تاریخ انتشار | 2018-11-11 |
| رتبه نشریه | علمی - پژوهشی |
| نوع نشریه | الکترونیکی |
| کشور محل چاپ | ایران |
چکیده مقاله
Abstract Drug resistance remains a major challenge in
the treatment of patients with ovarian cancer. Therefore,
the development of new anticancer drugs is a clinical
priority to develop more effective therapies. New approaches
to improve clinical outcomes and limit the
toxicity of anticancer drugs focus on chemoprevention.
The aim of this study was to determine the effects of
dendrosomal nanocurcumin (DNC) and oxaliplatin
(Oxa) and their combination on cell death and apoptosis
induction in human ovarian carcinoma cell lines analyzed
by MTT assay and flow cytometry, respectively.
The synergism effect of Oxa and DNC was analyzed
using the equation derived from Chou and Talalay. In
addition, real-time PCR was used to measure the effect
of this combination on the expression levels of long
non-coding RNAs with different expression in ovarian
cancer and normal ovaries. Our data showed that the
effect of DNC on cell death is more than curcumin alone
in the same concentration. The greatest cell death effect
was observed in combination of Oxa with DNC, while
Oxa was added first, followed by DNC at 4 h interval
(0/4 h). The findings indicated that DNC induced apoptosis
significantly in both cell lines as compared to
control groups; however, combination of both agents
had no significant effect in apoptosis induction. In addition,
combination of both agents significantly affects
the relative expression of long non-coding RNAs investigated
in the study as compared with mono therapy.