کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
8434089 | 1546634 | 2018 | 42 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Targeting autophagy by small molecule inhibitors of vacuolar protein sorting 34 (Vps34) improves the sensitivity of breast cancer cells to Sunitinib
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کلمات کلیدی
FGFRnuclear receptor coactivator 4microtubule-associated proteins 1A/1B light chain 3NCOA4PI3PBAFA1Vps34Chk1HCQATG7p62LC3HDACMcl-1HER2GFPmTORPI3KMCsAkt - آکتAutophagy - اتوفاژیErlotinib - ارلوتینیبcheckpoint kinase 1 - بازرسی کیناز 1bafilomycin A1 - بافیلومایسین A1Combination therapy - درمان ترکیبیphosphatidylinositol-3-kinase - فسفاتیدیلینواستیل-3-کینازphosphatidylinositol 3-phosphate - فسفاتیدیلینوزیتول 3-فسفاتhigh-content screening - نمایش محتویات بالاMechanistic target of rapamycin - هدف مکانیکی رپامایسینhydroxychloroquine - هیدروکسی کلروکینhistone deacetylase - هیستون داستیلازgreen fluorescent protein - پروتئین فلورسنت سبزprotein kinase B - پروتئین کیناز BMulticellular spheroids - کرویی چند سلولیChloroquine - کلروکین fibroblast growth factor receptor - گیرنده فاکتور رشد فیبروبلاست
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
تحقیقات سرطان
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
Resistance to chemotherapy is a challenging problem for treatment of cancer patients and autophagy has been shown to mediate development of resistance. In this study we systematically screened a library of 306 known anti-cancer drugs for their ability to induce autophagy using a cell-based assay. 114 of the drugs were classified as autophagy inducers; for 16 drugs, the cytotoxicity was potentiated by siRNA-mediated knock-down of Atg7 and Vps34. These drugs were further evaluated in breast cancer cell lines for autophagy induction, and two tyrosine kinase inhibitors, Sunitinib and Erlotinib, were selected for further studies. For the pharmacological inhibition of autophagy, we have characterized here a novel highly potent selective inhibitor of Vps34, SB02024. SB02024 blocked autophagy in vitro and reduced xenograft growth of two breast cancer cell lines, MDA-MB-231 and MCF-7, in vivo. Vps34 inhibitor significantly potentiated cytotoxicity of Sunitinib and Erlotinib in MCF-7 and MDA-MB-231 in vitro in monolayer cultures and when grown as multicellular spheroids. Our data suggests that inhibition of autophagy significantly improves sensitivity to Sunitinib and Erlotinib and that Vps34 is a promising therapeutic target for combination strategies in breast cancer.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Cancer Letters - Volume 435, 28 October 2018, Pages 32-43
Journal: Cancer Letters - Volume 435, 28 October 2018, Pages 32-43
نویسندگان
Matheus Dyczynski, Yasmin Yu, Magdalena Otrocka, Santiago Parpal, Tiago Braga, Aine Brigette Henley, Henric Zazzi, Mikael Lerner, Krister Wennerberg, Jenny Viklund, Jessica Martinsson, Dan Grandér, Angelo De Milito, Katja Pokrovskaja Tamm,