Targeting autophagy by small molecule inhibitors of vacuolar protein sorting 34 (Vps34) improves the sensitivity of breast cancer cells to Sunitinib

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. 11...

Celý popis

Uloženo v:

Podrobná bibliografie
Vydáno v:	Cancer letters Ročník 435; s. 32 - 43
Hlavní autoři:	Dyczynski, Matheus, Yu, Yasmin, Otrocka, Magdalena, Parpal, Santiago, Braga, Tiago, Henley, Aine Brigette, Zazzi, Henric, Lerner, Mikael, Wennerberg, Krister, Viklund, Jenny, Martinsson, Jessica, Grandér, Dan, De Milito, Angelo, Pokrovskaja Tamm, Katja
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	Ireland Elsevier B.V 28.10.2018 Elsevier Limited
Témata:	Autophagy Breast cancer Cancer therapies Cell culture Chemotherapy Combination therapy Cytotoxicity Drug development Drugs Erlotinib High-content screening Hypoxia Inhibitor drugs Kinases Libraries Medical screening Metabolism Oncology Phagocytosis Protein transport Protein-tyrosine kinase Proteins siRNA Spheroids Targeted cancer therapy Therapeutic applications Tumor cell lines Vps34 Xenografts Sweden MCL-1 Vps34 Chk1 Combination therapy Autophagy High-content screening GFP PI3P PI3K mTOR ATG7 LC3 NCOA4 AKT KU PROPPIN FGFR p62 CQ Erlotinib HCQ BafA1 HER2 MCS HDAC
ISSN:	0304-3835, 1872-7980, 1872-7980
On-line přístup:	Získat plný text
Tagy:	Přidat tag Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!

Popis
Shrnutí:	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. •High-Content screen identified 114 out of 306 anticancer drugs that induce autophagy.•Kinase inhibitors Sunitinib and Erlotinib induced autophagy in breast cancer cells.•We characterized SB02024, a novel highly potent and selective inhibitor of Vps34.•SB02024 reduced xenograft growth of the two breast cancer cell lines in vivo.•SB02024 increased kinase inhibitor-mediated cytotoxicity of breast cancer cells.
Bibliografie:	ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23
ISSN:	0304-3835 1872-7980 1872-7980
DOI:	10.1016/j.canlet.2018.07.028