کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
7623257 | 1494541 | 2016 | 13 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Differential pro-apoptotic effect of allicin in oestrogen receptor-positive or -negative human breast cancer cells
ترجمه فارسی عنوان
اثر متقابل پروپوپتوتیک آلیسین در سلولهای سرطان پستان انسانی مثبت یا ناسازگار گیرنده استروژن
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کلمات کلیدی
JC-1 (PubChem CID: 5492929)MTT (PubChem CID: 64965)Penicillin (PubChem CID: 5904)FITC (PubChem CID: 18730)HEPES (PubChem CID: 23831)KCl (PubChem CID: 4873)MAPK - MAPKAllicin - آلیسینEthanol (PubChem CID: 702) - اتانول (PubChem CID: 702)Streptomycin (PubChem CID: 19649) - استرپتومایسین (PubChem CID: 19649)Apoptosis - خزان یاختهایBreast cancer - سرطان پستانPropidium iodide (PubChem CID: 104981) - پرویدیم یود (PubChem CID: 104981)Glycerol (PubChem CID: 753) - گلیسرول (PubChem CID: 753)oestrogen receptor - گیرنده استروژن
موضوعات مرتبط
مهندسی و علوم پایه
شیمی
شیمی آنالیزی یا شیمی تجزیه
چکیده انگلیسی
Allicin is known to induce apoptosis and inhibit tumourigenesis in various carcinoma cells. However, the precise mechanism of allicin-induced apoptosis remains unclear in human breast cancer cells. Here we found that ERαâMDA-MB-231 cells were more sensitive to allicin-induced apoptosis as compared with ERα+MCF7 cells. We also found that allicin induced reactive oxygens species (ROS)-mediated and caspase-dependent apoptosis in MDA-MB-231 cells, but not in MCF7 cells. Additionally, we showed the p38 and JNK pathways were involved in allicin-induced apoptosis. Furthermore, we demonstrated that ERα-knockdown increased cell growth suppression and apoptosis of MCF7 cells in response to allicin, whereas ERα-overexpression decreased cell growth suppression and apoptosis of MDA-MB-231 cells, implicating that ERα has a protective role during allicin-induced apoptosis. Collectively, these findings suggest that allicin induces differential apoptotic pathways through MAPK activated by ROS-dependent or -independent signalling pathway in breast cancer cells.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Functional Foods - Volume 25, August 2016, Pages 341-353
Journal: Journal of Functional Foods - Volume 25, August 2016, Pages 341-353
نویسندگان
Kyung-Ho Kim, Seong-Jun Cho, Byung-Oh Kim, Suhkneung Pyo,