An In vitro Study on Curcumin Delivery by Nano-Micelles for Esophageal Squamous Cell Carcinoma (KYSE-۳۰)
- سال انتشار: 1397
- محل انتشار: مجله گزارش های بیوشیمی و زیست شناسی مولکولی، دوره: 6، شماره: 2
- کد COI اختصاصی: JR_RBMB-6-2_004
- زبان مقاله: انگلیسی
- تعداد مشاهده: 355
نویسندگان
Cancer Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
Department of Biology, Faculty of Sciences, Islamic Azad University-Mashhad Branch, Mashhad, Iran.
Department of Modern Sciences & Technologies, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Department of Biology, Faculty of Sciences, Islamic Azad University-Mashhad Branch, Mashhad, Iran.
Department of Biotechnology, Faculty of Medicine, Arak University of Medical Sciences, Arak, Iran.
School of Medicine, University of Birmingham, Birmingham, UK.
چکیده
Background: The incidence of esophageal squamous cell carcinoma (ESCC) is increasing, causing catastrophic health burdens on communities. Curcumin has shown promise as a therapeutic agent in the treatment of colon, colorectal, pancreatic, and esophageal cancers but it has very poor bioavailability. The application of nano-carriers as drug delivery systems increases curcuminchr('۳۹')s bioavailability. Cyclin D۱ is overexpressed in ESCC and curcumin may change its expression. Methods: In this study, the effect of SinaCurcumin®, a novel nano-micelle product containing ۸۰ mg curcumin, on the growth of KYSE-۳۰ cells and expression of cyclin D۱, was investigated. Paclitaxel and Carboplatin served as reference drugs. Results: Nano-curcumin increased cell cytotoxicity, decreased IC۵۰, and down-regulated of cyclin D۱. However, treatment of cells with nano-curcumin might result in multidrug resistance. Conclusions: Nano-curcumin suppressed proliferation of KYSE-۳۰ cells and expression of cyclin D۱ although its use in combination with other chemotherapeutic agents requires further testing.کلیدواژه ها
Curcumin, Cyclin D۱ gene, Drug resistance, KYSE-۳۰ cells, Nano-Micelleاطلاعات بیشتر در مورد COI
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