Non-benzoquinone geldanamycin analogs trigger various forms of death in human breast cancer cellsReport as inadecuate




Non-benzoquinone geldanamycin analogs trigger various forms of death in human breast cancer cells - Download this document for free, or read online. Document in PDF available to download.

Journal of Experimental and Clinical Cancer Research

, 35:149

First Online: 22 September 2016Received: 06 July 2016Accepted: 14 September 2016DOI: 10.1186-s13046-016-0428-6

Cite this article as: Zhang, Z., Li, HM., Zhou, C. et al. J Exp Clin Cancer Res 2016 35: 149. doi:10.1186-s13046-016-0428-6

Abstract

BackgroundHsp90 proteins are important therapeutic targets for many anti-cancer drugs in clinical trials. Geldanamycin GA was identified as the first natural inhibitor of Hsp90, increasing evidence suggests that GA was not a good choice for clinical trials. In this study, we investigated two new non-benzoquinone geldanamycin analogs of Hsp90 inhibitors, DHQ3 and 17-demethoxy-reblastatin 17-DR, to explore the molecular mechanisms of their anti-cancer activity in vivo and vitro.

MethodsMTT and colony formation assays were used to measure cell viability. Flow cytometry, DAPI staining, ATP assay, electron microscopy, western blots, siRNAs transfection and immunofluorescence were used to determine the molecular mechanism of DHQ3- or 17-DR-induced different forms of death in human breast cancer MDA-MB-231 cells. Malachite green reagent was used to measure ATPase activity of the analogs.

ResultsDHQ3 and 17-DR presented efficiently inhibitory effect in MDA-MB-231 cell lines, and DHQ3 induced necroptosis by activation of the RIP1-RIP3-MLKL necroptosis cascade. And DHQ3-induced cell death was inhibited by a necroptosis inhibitor, necrostatin-1 Nec-1, but not by a caspase inhibitor z-VAD-fmk. On the other hand, 17-DR induced apoptosis in MDA-MB-231 cells, indicating a caspase-dependent killing mechanism. We further demonstrated that down-regulation of RIP1 and RIP3 by siRNA protected against DHQ3 but not 17-DR induced cell death. These results were confirmed by electron microscopy. DHQ3 and 17-DR induced the degradation of Hsp90 client proteins, and they showed strong antitumor effects in MDA-MB-231 cell-xenografted nude mice.

ConclusionsThese findings supported that DHQ3 and 17-DR induce different forms of death in some cancer cell line via activation of different pathways. All of the results provided evidence for its anti-tumorigentic action with low hepatotoxicity in vivo, making them promising anti-breast cancer agents.

KeywordsGeldanamycin analogs Hsp90 Necroptosis Apoptosis Breast cancer Abbreviations17-DR17-demethoxy-reblastatin

AktSerine-threonine kinase

ALTAlanine-aminotransferase

ASTAspartate aminotransferase

BSABovine serum albumin

CDK4Cyclin dependent kinase 4

C-RafRaf proto-oncogene serine-threonine-protein kinase

DAPI4,6-diamidino-2-phenylindole

DMEMDulbecco’s modified Eagle’s medium

DMSODimethyl sulfoxide

EGFREpidermal growth factor receptor

FBSFetal bovine serum

GAGeldanamycin

HCCHuman hepatocellular carcinoma

Her2Human epidermal growth factor receptor 2

HIF1aHypoxia-inducible factor

HSPsHeat shock proteins

MLKLMixed lineage kinase domain-like protein

MTT3-4,5-Dimethylthiazol-2-yl-2,5-diphenyltetrazolium bromide

Nec-1Necrostatin-1

PBSPhosphate-buffered saline

PIPropidium iodide

PVDFPolyvinylidene fluoride

RIPReceptor-interacting protein

RPMI-1640Roswell park memorial institute-1640 medium

SDS-PAGESodium dodecyl sulfate-polyacrylamide gel electrophoresis

TNBCTriple-negative breast cancers

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Author: Zhirui Zhang - Hong-Mei Li - Can Zhou - Qixiang Li - Linyan Ma - Zixuan Zhang - Yiming Sun - Lirong Wang - Xudong Zhang -

Source: https://link.springer.com/







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