Literature DB >> 19940992

Putative chemopreventive molecules can increase Nrf2-regulated cell defense in some human cancer cell lines, resulting in resistance to common cytotoxic therapies.

Liangao Hu1, Weimin Miao, Martin Loignon, Mustapha Kandouz, Gerald Batist.   

Abstract

Nrf2 is a key transcription factor, which induces a cytoprotective gene array. Nrf2 is regulated at the posttranslational level through proteasomal degradation through an interaction with the adapter protein Keap1. High levels of Nrf2, resulting from a loss of function mutation in Keap1, were reported in chemoresistant non-small cell lung cancer. We observed very low levels of Nrf2 and of Nrf2-regulated detoxification proteins as a frequent phenotype in the more chemosensitive breast cancer, and when engineering increased Nrf2 levels, we found resistance to both doxorubicin and paclitaxel. We here show that basal Nrf2 levels in different cell lines correlate with their respective sensitivity to a common cytotoxic chemotherapy. Nrf2 and its regulated genes and proteins are the targets of a major strategy in cancer prevention. Molecules that interfere with the Nrf2-Keap1-Cul3 protein-protein interactions result in higher levels of Nrf2. Both naturally occurring and synthetic molecules with this effect have been suggested as clinical chemopreventive agents, including molecules derived from cruciferous vegetables such as the isothiocyanate sulforaphane and even green tea polyphenols. Here, we determine the impact of these putative chemopreventive agents on the sensitivity of established cancer cell lines to chemotherapy. We confirmed that these molecules do increase Nrf2 and detoxification enzyme levels in breast cancer cell lines with very low basal Nrf2 levels, and this is associated with significant chemoresistance to cytotoxic drugs. Both effects are less in another breast cancer cell line with intermediate Nrf2, and in lung cancer cells with high Nrf2, these same molecules have no effect on Nrf2 but do actually enhance chemoresistance. While the details of dose and schedule of these agents require further study in in vivo models, these data sound a cautionary note for the use of these agents in patients with established cancers who are undergoing chemotherapy treatment.

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Year:  2009        PMID: 19940992     DOI: 10.1007/s00280-009-1182-7

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  25 in total

1.  Prognosis of hormone-dependent breast cancer seems to be influenced by KEAP1, NRF2 and GSTM1 genetic polymorphisms.

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2.  Dicoumarol enhances gemcitabine-induced cytotoxicity in high NQO1-expressing cholangiocarcinoma cells.

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Journal:  World J Gastroenterol       Date:  2010-05-21       Impact factor: 5.742

Review 3.  Current clinical regulation of PI3K/PTEN/Akt/mTOR signalling in treatment of human cancer.

Authors:  Hui Jun Lim; Philip Crowe; Jia-Lin Yang
Journal:  J Cancer Res Clin Oncol       Date:  2014-08-22       Impact factor: 4.553

4.  Focal, periocular delivery of 2-deoxy-D-glucose as adjuvant to chemotherapy for treatment of advanced retinoblastoma.

Authors:  Yolanda Piña; Samuel K Houston; Timothy G Murray; Hinda Boutrid; Magda Celdran; William Feuer; Wei Shi; Eleut Hernandez; Theodore J Lampidis
Journal:  Invest Ophthalmol Vis Sci       Date:  2010-08-11       Impact factor: 4.799

Review 5.  The chemopreventive and chemotherapeutic potentials of tea polyphenols.

Authors:  Vijay S Thakur; Karishma Gupta; Sanjay Gupta
Journal:  Curr Pharm Biotechnol       Date:  2012-01       Impact factor: 2.837

Review 6.  The effects of chromium(VI) on the thioredoxin system: implications for redox regulation.

Authors:  Charles R Myers
Journal:  Free Radic Biol Med       Date:  2012-04-18       Impact factor: 7.376

7.  Arsenic inhibits autophagic flux, activating the Nrf2-Keap1 pathway in a p62-dependent manner.

Authors:  Alexandria Lau; Yi Zheng; Shasha Tao; Huihui Wang; Samantha A Whitman; Eileen White; Donna D Zhang
Journal:  Mol Cell Biol       Date:  2013-04-15       Impact factor: 4.272

8.  Effects of ATRA combined with citrus and ginger-derived compounds in human SCC xenografts.

Authors:  Heather E Kleiner-Hancock; Runhua Shi; Angela Remeika; Delira Robbins; Misty Prince; Jennifer N Gill; Zanobia Syed; Patrick Adegboyega; J Michael Mathis; John L Clifford
Journal:  BMC Cancer       Date:  2010-07-26       Impact factor: 4.430

9.  Benzo[a]pyrene increases the Nrf2 content by downregulating the Keap1 message.

Authors:  Phuong Minh Nguyen; Miki Susanto Park; Marilynn Chow; Jae H Chang; Lisa Wrischnik; William K Chan
Journal:  Toxicol Sci       Date:  2010-05-23       Impact factor: 4.849

Review 10.  Arsenic-mediated activation of the Nrf2-Keap1 antioxidant pathway.

Authors:  Alexandria Lau; Samantha A Whitman; Melba C Jaramillo; Donna D Zhang
Journal:  J Biochem Mol Toxicol       Date:  2012-11-27       Impact factor: 3.642

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