Journal article

ATF3 repression of BCL-XL determines apoptotic sensitivity to HDAC inhibitors across tumor types

AC Chüeh, JWT Tse, M Dickinson, P Ioannidis, L Jenkins, L Togel, BS Tan, I Luk, M Davalos-Salas, R Nightingale, MR Thompson, BRG Williams, G Lessene, EF Lee, WD Fairlie, AS Dhillon, JM Mariadason

Clinical Cancer Research | AMER ASSOC CANCER RESEARCH | Published : 2017

Abstract

Purpose: Histone deacetylase inhibitors (HDACi) are epigenome-targeting small molecules approved for the treatment of cutaneous T-cell lymphoma and multiple myeloma. They have also demonstrated clinical activity in acute myelogenous leukemia, non–small cell lung cancer, and estrogen receptor–positive breast cancer, and trials are underway assessing their activity in combination regimens including immunotherapy. However, there is currently no clear strategy to reliably predict HDACi sensitivity. In colon cancer cells, apoptotic sensitivity to HDACi is associated with transcriptional induction of multiple immediate-early (IE) genes. Here, we examined whether this transcriptional response predi..

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Grants

Awarded by Ludwig Institute for Cancer Research


Funding Acknowledgements

This study was funded by the National Health and Medical Research Council (NHMRC) of Australia (1008833 and 1066665), The National Institutes of Health (NIH1RO1 CA123316), an Australian Research Council Future Fellowship (FT0992234), an NHMRC Senior Research Fellowship (1046092) to J.M. Mariadason, Ludwig Cancer Research, and the Operational Infrastructure Support Program, Victorian Government, Australia. J.W.T. Tse was supported by an Australian Postgraduate Award.