Page 7 - Read Online
P. 7

Topic: Cancer Stem Cells: Impact on Treatment


            Introduction to the Special Issue “Cancer Stem Cells: Impact on
            Treatment”

            Ira-Ida Skvortsova
            Laboratory for Experimental and Translational Research on Radiation Oncology (EXTRO-Lab), Department of Therapeutic Radiology and
            Oncology, Innsbruck Medical University, 6020 Innsbruck, Austria.
            Correspondence to: Dr. Ira-Ida Skvortsova, Laboratory for Experimental and Translational Research on Radiation Oncology (EXTRO-Lab),
            Department of Therapeutic Radiology and Oncology, Innsbruck Medical University, 6020 Innsbruck, Austria. E-mail: Ira.Skvortsova@i-med.ac.at

            Despite the fact that  currently existing  therapeutic   of curcumin can accelerate proliferation of the leukemic
            approaches are highly effective and can markedly improve   cells  and  application  of  5-fluorouracil  becomes  more
            clinical  outcome in cancer patients with even advanced   effective  compared  to  the  treatment  with  5-fluorouracil
            diseases,  the  problems  of treatment  resistance,  therapy   without  curcumin.  These  findings  help  to  assume  that
            recurrences  and  unfavorable  disease  progression are   administration  of the compounds affecting  quiescence
            still not solved. It is generally believed  that the small   of carcinoma cells can improve therapy results in cancer
            population of the intratumoral carcinoma stem cells (CSCs)   patients with malignant tumors containing a high number
            is  responsible  for  poor  clinical  outcome,  because  CSCs   of quiescent CSCs.
            are considered as a reason for the tumor heterogeneity,
            diminished  sensitivity  to chemo- and radiotherapy  and   Review  article  by Kim  et  al.  highlights  therapeutic
                                                                                        [11]
            enhanced abilities for metastatic spread. [1-5]  Investigation   opportunities to target CSCs and to reach better treatment
            of the biological properties of CSCs is a hot topic in cancer   results in cancer patients. Recent years have seen an

            research. In order to know more about CSC behavior, it is   increased number of research reports on the CSC-related
            necessary to possess the CSC-specific molecular patterns   intracellular and intratumoral molecular pathways that can
            distinguishing  CSCs from  non-CSCs. Using currently
            existing surrogate CSC biomarkers [CD133 (prominin-1),   be effectively  blocked  in  order to reach  better  survival
            CD44, CD24, Bmi-1, Notch family members, Hedgehog,   rate in cancer  patients.  This review article  provides an
            aldehyde dehydrogenase 1 (ALDH1),  nestin,  etc.],   analysis of different strategies that can be introduced into
            subpopulations carcinoma cells with stem cell properties   the clinical practice in order to improve therapy outcome
            can be  isolated for further  investigations.  Recent   in patients with unfavourable prognosis.
                                                  [2]
            studies have demonstrated  that a variety  of intracellular
            pathways are affected  in CSCs: CSC metabolism  is   The Guest Editor and contributors to this special issue of
            characterized by activation of glycolytic pathways  and   the journal Journal of Cancer Metastasis and Treatment
                                                      [6]
            intracellular redox potential is dysregulated; [1,7,8]  molecular   hope that basic researchers and clinicians will read these
            mechanisms governing cell cycle, cell proliferation  and   articles with great interest.
            cell death development are also disrupted. Thus, there is
            a hypothesis that one of the reasons of CSC insensitivity   Acknowledgments
            to chemotherapeutics and ionizing radiation is the slower   I am heartily thankful and owe my deepest gratitude to
            CSC proliferation and CSC quiescence.  It is known that   Dandan Yu and Lisa Huang for their boundless readiness
                                            [1]
            chemotherapeutic  agents  and  radiotherapy  eradicate  fast   to help and assist during processing of the  submitted
            dividing and proliferating carcinoma cells more effectively   articles and in the preparation of this issue.
            than the slower dividing cells.  Therefore, it is logical to
                                     [1]
            suggest that quiescent CSCs should be changed in their   Financial support and sponsorship
            intracellular  signalings  underlying  cell  cycle  regulation   Nil.
            and cell division. Indeed, Gardane et al.  and Vaidya
                                                         [10]
                                              [9]
            in their article have clearly demonstrated that low doses   This is an open access article distributed under the terms of the Creative
                                                              Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows
                                                              others to remix, tweak, and build upon the work non-commercially, as long as
                            Access this article online        the author is credited and the new creations are licensed under the identical
                                                              terms.
               Quick Response Code:
                                  Website:                    For reprints contact: service@oaepublish.com
                                  http://www.jcmtjournal.com
                                                               How to cite this article: Skvortsova II. Introduction to the Special
                                                               Issue “Cancer Stem Cells: Impact on Treatment”. J Cancer Metasta
                                  DOI:                         Treat 2016;2:231-2.
                                  10.20517/2394-4722.2016.35
                                                               Received: 17-06-2016; Accepted: 19-06-2016.

                        ©2016 Journal of Cancer Metastasis and Treatment ¦ Published by OAE Publishing Inc.  231
   2   3   4   5   6   7   8   9   10   11   12