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International Journal of CancerVolume 134, Issue 6, 15 March 2014, Pages 1270-1278

Therapy-induced enrichment of putative lung cancer stem-like cells(Article)

  • aCancer Drug Resistance Group, Institute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal
  • bExpression Regulation in Cancer Group, Institute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal
  • cPublic Awareness of Cancer Unit, Institute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal
  • dFaculty of Medicine, University of Porto, Porto, Portugal
  • eDepartment of Biochemistry and Molecular Biology, Eppley Institute, University of Nebraska Medical Center, Omaha, United States
  • fDepartment of Biological Sciences, Faculty of Pharmacy, University of Porto, Porto, Portugal

Abstract

Tumour drug resistance is a major issue in the management of lung cancer patients as almost all lung tumours are either intrinsically resistant or quickly develop acquired resistance to chemotherapeutic drugs. Cancer drug resistance has recently been linked, at least in part, to the existence of cancer stem-like cells (CSLCs), a small sub-population of cells within the tumour that possess stem-like properties. CSLCs are often isolated by fluorescence activated cell sorting (FACS) according to the expression of certain stem-like cell membrane markers. Conflicting results regarding the specificity of particular stem cell surface markers for isolating CSLCs have, however, been recently reported. Therefore, alternative strategies enabling the identification and study of CSLCs should be considered, particularly in tumour types where appropriate stem cell markers are not well established and validated, like in lung cancer. In this article, we review data indicating therapy-selection as a valid approach for putative lung CSLCs enrichment. We believe that this strategy would be determinant for correctly assessing and characterising the sub-populations of CSLCs that are able to survive chemo or radiotherapy regimens and, at the same time, also have the ability to recapitulate and sustain tumour growth. Using therapy-induced enrichment of CSLCs may, therefore, prove to be an extremely useful method for studying CSLCs and provide new clues regarding potential therapeutic targets for their efficient elimination, which will undoubtedly play a decisive role in improving lung cancer patients' survival. © 2013 UICC.

Author keywords

cancer stem-like cellsdrug resistancelung cancerradiation resistancetumour recurrence

Indexed keywords

EMTREE drug terms:cisplatindocetaxeldoxorubicinerlotinibetoposidefluorouracilgefitinibmethotrexatepaclitaxel
EMTREE medical terms:articlecancer chemotherapycancer radiotherapycancer stem cellcancer stem like cellcancer therapycarcinogenicitycell survivaldrug responsehumanlung cancerlung non small cell cancerlung small cell cancernonhumanpriority journalradiosensitivitytherapy resistancetumor growth

Chemicals and CAS Registry Numbers:

cisplatin, 15663-27-1, 26035-31-4, 96081-74-2; docetaxel, 114977-28-5; doxorubicin, 23214-92-8, 25316-40-9; erlotinib, 183319-69-9, 183321-74-6; etoposide, 33419-42-0; fluorouracil, 51-21-8; gefitinib, 184475-35-2, 184475-55-6, 184475-56-7; methotrexate, 15475-56-6, 59-05-2, 7413-34-5; paclitaxel, 33069-62-4

  • ISSN: 00207136
  • CODEN: IJCNA
  • Source Type: Journal
  • Original language: English
  • DOI: 10.1002/ijc.28478
  • Document Type: Article

  Almeida, G.M.; Institute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Rua Dr. Roberto Frias s/n, Portugal;
© Copyright 2014 Elsevier B.V., All rights reserved.

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