Literature DB >> 21329798

Analysis of nelfinavir-induced endoplasmic reticulum stress.

Ansgar Brüning1.   

Abstract

Nelfinavir (Viracept®) is an HIV protease inhibitor that has been shown to induce the endoplasmic reticulum (ER) stress reaction in human cancer cells. Although the presumed drug doses needed for an efficient ER stress reaction and ensuing apoptosis in cancer cells is somewhat higher than those prescribed for HIV-infected persons, nelfinavir represents one of the few clinically applicable ER stress-inducing agents, and is currently being tested in clinical studies on cancer patients. Therefore, this chapter describes how to obtain and use nelfinavir for in vitro and in vivo studies. In addition, methods are described that might facilitate the analysis and monitoring of the nelfinavir-induced ER stress response either in cancer cells in cell culture or in cancer tissue biopsies. These methods include various fluorescence-based ER staining techniques and the expression analysis of primary and secondary ER stress markers by immunoblotting and RT-PCR analysis. Among the several methods presented, the analysis of an unconventional XBP1 splicing, caused by the ER stress sensor IRE1, is shown to present the most sensitive and most specific marker for nelfinavir-induced ER stress. Primers and PCR conditions suitable for XBP1 PCR and splicing analysis are presented. Such a PCR-based XBP1 splicing analysis might not only be suitable to monitor nelfinavir-induced ER stress, but could also be applied in drug screening programs to test for other ER stress-inducing agents with similar activities or synergistic activities with nelfinavir.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21329798     DOI: 10.1016/B978-0-12-385928-0.00008-0

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  12 in total

1.  Human immunodeficiency virus protease inhibitors modulate Ca2+ homeostasis and potentiate alcoholic stress and injury in mice and primary mouse and human hepatocytes.

Authors:  Eddy Kao; Masao Shinohara; Min Feng; Mo Yin Lau; Cheng Ji
Journal:  Hepatology       Date:  2012-06-11       Impact factor: 17.425

2.  Proteasome inhibition by quercetin triggers macroautophagy and blocks mTOR activity.

Authors:  Anja K Klappan; Stefanie Hones; Ioannis Mylonas; Ansgar Brüning
Journal:  Histochem Cell Biol       Date:  2011-10-13       Impact factor: 4.304

Review 3.  Insights into the broad cellular effects of nelfinavir and the HIV protease inhibitors supporting their role in cancer treatment and prevention.

Authors:  Soren Gantt; Corey Casper; Richard F Ambinder
Journal:  Curr Opin Oncol       Date:  2013-09       Impact factor: 3.645

4.  Nelfinavir and bortezomib inhibit mTOR activity via ATF4-mediated sestrin-2 regulation.

Authors:  Ansgar Brüning; Martina Rahmeh; Klaus Friese
Journal:  Mol Oncol       Date:  2013-07-20       Impact factor: 6.603

5.  Identification of endoplasmic reticulum stress-inducing agents by antagonizing autophagy: a new potential strategy for identification of anti-cancer therapeutics in B-cell malignancies.

Authors:  Emilia Mahoney; Kami Maddocks; Joseph Flynn; Jeffrey Jones; Sara L Cole; Xiaoli Zhang; John C Byrd; Amy J Johnson
Journal:  Leuk Lymphoma       Date:  2013-04-16

6.  Disulfiram/copper causes redox-related proteotoxicity and concomitant heat shock response in ovarian cancer cells that is augmented by auranofin-mediated thioredoxin inhibition.

Authors:  Margarita Papaioannou; Ioannis Mylonas; Richard E Kast; Ansgar Brüning
Journal:  Oncoscience       Date:  2013-12-11

7.  Subverting ER-stress towards apoptosis by nelfinavir and curcumin coexposure augments docetaxel efficacy in castration resistant prostate cancer cells.

Authors:  Aditi Mathur; Zakaria Y Abd Elmageed; Xichun Liu; Mikhail L Kostochka; Haitao Zhang; Asim B Abdel-Mageed; Debasis Mondal
Journal:  PLoS One       Date:  2014-08-14       Impact factor: 3.240

8.  Endoplasmic reticulum stress and cell death in mTORC1-overactive cells is induced by nelfinavir and enhanced by chloroquine.

Authors:  Charlotte E Johnson; David K Hunt; Marie Wiltshire; Terry P Herbert; Julian R Sampson; Rachel J Errington; D Mark Davies; Andrew R Tee
Journal:  Mol Oncol       Date:  2014-11-22       Impact factor: 6.603

Review 9.  A conceptually new treatment approach for relapsed glioblastoma: coordinated undermining of survival paths with nine repurposed drugs (CUSP9) by the International Initiative for Accelerated Improvement of Glioblastoma Care.

Authors:  Richard E Kast; John A Boockvar; Ansgar Brüning; Francesco Cappello; Wen-Wei Chang; Boris Cvek; Q Ping Dou; Alfonso Duenas-Gonzalez; Thomas Efferth; Daniele Focosi; Seyed H Ghaffari; Georg Karpel-Massler; Kirsi Ketola; Alireza Khoshnevisan; Daniel Keizman; Nicolas Magné; Christine Marosi; Kerrie McDonald; Miguel Muñoz; Ameya Paranjpe; Mohammad H Pourgholami; Iacopo Sardi; Avishay Sella; Kalkunte S Srivenugopal; Marco Tuccori; Weiguang Wang; Christian R Wirtz; Marc-Eric Halatsch
Journal:  Oncotarget       Date:  2013-04

Review 10.  Role of endoplasmic reticulum stress in drug-induced toxicity.

Authors:  Fabienne Foufelle; Bernard Fromenty
Journal:  Pharmacol Res Perspect       Date:  2016-02-04
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