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Chang et al. J Cancer Metastasis Treat 2019;5:78                    Journal of Cancer
               DOI: 10.20517/2394-4722.2019.31                           Metastasis and Treatment




               Review                                                                        Open Access


               Histone chaperone FACT and curaxins: effects on
               genome structure and function


               Han-Wen Chang , Ekaterina V. Nizovtseva , Sergey V. Razin , Tim Formosa , Katerina V. Gurova , Vasily
                                                                                4
                                                                  2,3
                                                                                                 5
                             1
                                                   1
               M. Studitsky 1,3
               1 Cancer Epigenetics Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
               2 Institute of Gene Biology RAS, Moscow 119334, Russia.
               3 Biology Faculty, Lomonosov Moscow State University, Moscow 119992, Russia.
               4 Department of Biochemistry, University of Utah School of Medicine, Salt Lake City, Utah 84132, USA.
               5 Department of Cell Stress Biology, Roswell Park Cancer Institute, Buffalo, NY 14263, USA.
               Correspondence  to: Prof. Vasily M. Studitsky, Cancer Epigenetics Program, Fox Chase Cancer Center, 333 Cottman Ave.,
               Philadelphia, PA 19111, USA. E-mail: vasily.studitsky@fccc.edu

               How to cite this article: Chang HW, Nizovtseva EV, Razin SV, Formosa T, Gurova KV, Studitsky VM. Histone chaperone FACT
               and curaxins: effects on genome structure and function. J Cancer Metastasis Treat 2019;5:78.
               http://dx.doi.org/10.20517/2394-4722.2019.31

               Received: 2 Sep 2019    First Decision: 4 Nov 2019     Revised: 12 Nov 2019    Accepted: 14 Nov 2019    Published: 29 Nov 2019

               Science Editor: Godefridus J. Peters    Copy Editor: Jing-Wen Zhang    Production Editor: Tian Zhang


               Abstract
               The histone chaperone facilitates chromatin transcription (FACT) plays important roles in essentially every
               chromatin-associated process and is an important indirect target of the curaxin class of anti-cancer drugs.
               Curaxins are aromatic compounds that intercalate into DNA and can trap FACT in bulk chromatin, thus interfering
               with its distribution and its functions in cancer cells. Recent studies have provided mechanistic insight into how
               FACT and curaxins cooperate to promote unfolding of nucleosomes and chromatin fibers, resulting in genome-
               wide disruption of contact chromatin domain boundaries, perturbation of higher-order chromatin organization,
               and global dysregulation of gene expression. Here, we discuss the implications of these insights for cancer biology.


               Keywords: Genomics, transcription, nucleosomes, chromatin structure




               INTRODUCTION
               Facilitates chromatin transcription (FACT) is a highly conserved histone chaperone that participates
                                              [1]
                                                                     [2-8]
               in multiple physiological processes  including transcription , DNA replication [9-13] , DNA repair [14-17] ,
                           © The Author(s) 2019. Open Access This article is licensed under a Creative Commons Attribution 4.0
                           International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use,
                sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long
                as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license,
                and indicate if changes were made.


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