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Morgan et al. J Cancer Metastasis Treat 2017;3:278-87                               Journal of
           DOI: 10.20517/2394-4722.2017.31
                                                             Cancer Metastasis and Treatment

                                                                                               www.jcmtjournal.com
            Topic: How does the prostate cancer microenvironment affect   Topic:                Open Access
            the metastatic process and/or treatment outcome?

           HOX transcription factors and the prostate
           tumor microenvironment




           Richard Morgan , Hardev S. Pandha 2
                         1
           1 Institute of Cancer Therapeutics, Faculty of Life Sciences, University of Bradford, Bradford BD7 1DP, UK.
           2 Faculty of Health and Medical Sciences, University of Surrey, Guildford, Surrey GU2 7XH, UK.
           Correspondence to: Prof. Richard Morgan, Institute of Cancer Therapeutics, Faculty of Life Sciences, University of Bradford, Bradford BD7 1DP,
           UK. E-mail: r.morgan3@bradford.ac.uk

           How to cite this article: Morgan R, Pandha HS. HOX transcription factors and the prostate tumor microenvironment. J Cancer Metastasis Treat
           2017;3:278-87.
                                         ABSTRACT
            Article history:              It is now well established that the tumor microenvironment plays an essential role in the
            Received: 15 May 2017         survival, growth, invasion, and spread of cancer through the regulation of angiogenesis
            First Decision: 3 Jul 2017    and localized immune responses. This review examines the role of the HOX genes, which
            Revised: 7 Jul 2017           encode a family of homeodomain-containing transcription factors, in the interaction
            Accepted: 14 Aug 2017         between prostate tumors and their microenvironment. Previous studies have established
            Published: 6 Dec 2017         that  HOX genes have an important function in prostate cancer cell survival  in vitro
            Key words:                    and  in vivo, but there is also evidence that HOX proteins regulate the expression of
            Prostate cancer,              genes in the cancer cell that influence the tumor microenvironment, and that cells in the
            tumor microenvironment,       microenvironment likewise express HOX genes that confer a tumor-supportive function.
            HOX,                          Here we provide an overview of these studies that, taken together, indicate that the HOX
            PBX,                          genes help mediate cross talk between prostate tumors and their microenvironment.
            metastasis,
            angiogenesis

           INTRODUCTION                                       HOX family of transcription factors in the interaction
                                                              between prostate tumors and their microenvironment.
           In addition to cancer cells, tumor tissue contains a
           variety of host cells, extracellular matrix components,   THE HOX GENES
           and  secreted  proteins  that  together  constitute  the
           tumor microenvironment . Crosstalk between the     Early embryonic development is characterized by a
                                  [1]
           tumor and its microenvironment has an important role   number of overlapping signaling events that give rise
           in tumor development, including the recruitment of   to stable transcriptional states and these in turn confer
           immune  cells  and  vascular  cells,  both  of  which  can   specific identities at both the cellular and tissue level.
           have  profound  effects  on  the  survival  and  spread   Many of the transcription factors that are responsible
           of the tumor and are therefore targets for cancer   for regulating embryonic development were originally
           therapy [2-4] . In this review, we consider the role of the   characterized by the distinct phenotypes caused by
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            278  © The Author(s) 2017                                                                                                                                 www.oaepublish.com
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