کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5862447 1133780 2013 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Carboplatin resistant human laryngeal carcinoma cells are cross resistant to curcumin due to reduced curcumin accumulation
ترجمه فارسی عنوان
سلول های کارسینومار حنجره انسانی مقاوم به کاربوپلاتین به علت کاهش تجمع کورکومین به کورکومین مقاوم هستند
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست بهداشت، سم شناسی و جهش زایی
چکیده انگلیسی

Curcumin is a natural compound that exhibits a wide range of beneficial effects, among them the anti-tumor activity. Recently it was shown that curcumin may be efficient against drug resistant tumor cells. The goal of our investigation was to examine if human laryngeal carcinoma cells resistant to carboplatin display sensitivity to curcumin, as compared to parental cells, and if this sensitivity is altered, to determine the molecular mechanisms that are responsible for it. We found that carboplatin resistant 7T cells were also cross resistant to curcumin. After the treatment with equimolar concentration of curcumin, 7T cells exhibited lower intracellular accumulation of curcumin which coincided with reduced formation of reactive oxygen species (ROS), diminished lipid and DNA damage followed by reduced induction of apoptosis and expression of heat shock protein 70 (Hsp70), as compared to parental HEp-2 cells. However, after the treatment with equitoxic concentration of curcumin, intracellular accumulation and all the explored downstream effects were similar in both cell lines suggesting that resistance of 7T cells to curcumin was based on its reduced intracellular accumulation. Since curcumin accumulates mostly in the membranes, we explored the fatty acid composition of both cell lines, but we did not find any difference between them.

► Carboplatin resistant laryngeal carcinoma 7T cells are cross resistant to curcumin. ► Reduced accumulation of curcumin is involved in curcumin resistance of 7T cells. ► Curcumin induces less ROS, lipid and DNA damage and apoptosis in 7T cells.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Toxicology in Vitro - Volume 27, Issue 2, March 2013, Pages 523-532
نویسندگان
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