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ALHulais et al. J Cancer Metastasis Treat 2019;5:3                  Journal of Cancer
               DOI: 10.20517/2394-4722.2018.71                           Metastasis and Treatment




               Review                                                                        Open Access


               Cancer stem cells, stemness markers and selected
               drug targeting: metastatic colorectal cancer and

               cyclooxygenase-2/prostaglandin E2 connection to
               WNT as a model system


               Reem Ali ALHulais, Stephen John Ralph

               School of Medical Sciences, Griffith University, Menzies Health Institute Queensland, Gold Coast, QLD 4222, Australia.
               Correspondence to: Dr. Stephen John Ralph, School of Medical Sciences, Griffith University, Menzies Health Institute
               Queensland, Gold Coast, QLD 4222, Australia. E-mail: s.ralph@griffith.edu.au

               How to cite this article: ALHulais RA, Ralph SJ. Cancer stem cells, stemness markers and selected drug targeting: metastatic
               colorectal cancer and cyclooxygenase-2/prostaglandin E2 connection to WNT as a model system. J Cancer Metastasis Treat
               2019;5:3. http://dx.doi.org/10.20517/2394-4722.2018.71

               Received: 1 Nov 2018    First Decision: 5 Dec 2018    Revised: 5 Dec 2018    Accepted: 25 Dec 2018    Published: 21 Jan 2019

               Science Editor: Umberto Galderisi    Copy Editor: Cai-Hong Wang    Production Editor: Huan-Liang Wu



               Abstract
               Few studies have reported on the analyses of drugs targeting enriched populations of cancer stem cells (CSCs) as
               a means for identifying potent anti-CSC agents. This review evaluates recent information on the identification and
               functions of specific CSC surface markers, with particular emphasis on colorectal cancers and the screening of
               drugs to eliminate such cells. Many of these CSC markers are found commonly expressed on CSCs from different
               cancer types as well as embryonic stem cells. These markers are often related to hypoxic activation of the WNT/
               b-catenin pathway, cyclooxygenase-2/prostaglandin E signalling and their relationship to LGR5. By effectively
               using drugs that inhibit these pathways to kill the CSC population, or otherwise forcing them out of dormancy
               into active cell division, cancers should become more susceptible to chemotherapy. Such combinational therapies
               targeting both CSCs and proliferating tumor cells should greatly improve upon the current basis for treatment.

               Keywords: Cancer stem cells, colorectal cancer, markers, selective drug targeting




               GENERAL BACKGROUND TO CANCER STEM CELLS
               Our understanding of the roles played by cancer stem cells (CSCs), their importance during the progression
               of cancer and justification for why they should be specifically targeted to eliminate cancer as a disease
               remains limited. Evidence supporting the “cancer stem cell” hypothesis is mounting such that CSC existence

                           © 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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