4.6 Review

Deubiquitylating enzymes as cancer stem cell therapeutics

Journal

BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER
Volume 1869, Issue 1, Pages 1-10

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.bbcan.2017.10.004

Keywords

Cancer stem cells; Cellular reprogramming; Direct conversion; DUB inhibitors; Protein induced pluripotent stem cells; Yamanaka factors

Funding

  1. National Research Foundation of Korea [2015R1C1A1A01054482, 2015R1D1A1A01060907, 2017M3A9C6061361]
  2. Medical Research Center - National Research Foundation of Korea (NRF) of the Ministry of Science, ICT and Future Planning, Republic of Korea [2017R1A5A2015395]
  3. Bio and Medical Technology Development Program of the National Research Foundation (NRF)
  4. Korean government (MSIP) [2017M3A9E4048172]
  5. Korean government (MOHW) [2017M3A9E4048172]

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The focus of basic and applied research on core stem cell transcription factors has paved the way to initial delineation of their characteristics, their regulatory mechanisms, and the applicability of their regulatory proteins for protein-induced pluripotent stem cells (protein-IPSC) generation and in further clinical settings. Striking parallels have been observed between cancer stem cells (CSCs) and stem cells. For the maintenance of stem cells and CSC pluripotency and differentiation, post translational modifications (i.e., ubiquitylation and deubiquitylation) are tightly regulated, as these modifications result in a variety of stem cell fates. The identification of deubiquitylating enzymes (DUBs) involved in the regulation of core stem cell transcription factors and CSC related proteins might contribute to providing novel insights into the implications of DUB regulatory mechanisms for governing cellular reprogramming and carcinogenesis. Moreover, we propose the novel possibility of applying DUBs coupled with core transcription factors to improve protein-iPSC generation efficiency. Additionally, this review article further illustrates the potential of applying DUB inhibitors as a novel therapeutic intervention for targeting CSCs. Thus, defining DUBs as core pharmacological targets implies that future endeavors to develop their inhibitors may revolutionize our ability to regulate stem cell maintenance and differentiation, somatic cell reprogramming, and cancer stem cells.

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