Cited by 199Cancer Cells and MetastasisMesenchymal stem cell researchHematopoietic Stem Cell Transplantation

Mechanisms of Disease: Cancer stem cells--targeting the evil twin

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Trumpp, Andreas, Wiestler, Otmar D·2008·Nature Clinical Practice Oncology

Abstract

Classical antineoplastic treatments such as chemotherapy or radiation can efficiently eradicate the majority of proliferating and genetically unstable malignant cells within neoplastic lesions. There is increasing evidence, however, that these regimens frequently fail to eliminate a minor subpopulation of resistant tumor cells that have distinct features of somatic stem cells. These serve as a reservoir for disease recurrence, and are the origin of metastatic growth. These so-called cancer stem cells (CSCs) or cancer-initiating cells represent often a rare, highly self-renewing population within the tumor mass, which is thought to be the only one required for both initiation and maintenance of disease. Tumor-cell populations enriched for CSC activity were originally identified in leukemias, but have now also been uncovered in a number of solid cancers. Their marked resistance towards classical antitumor regimens is mediated by the combination of several critical features, including relative dormancy, efficient DNA repair, high expression of multidrug-resistance-type membrane transporters and protection by a hypoxic niche environment. We review the concept of CSCs with particular emphasis on the mechanism of therapy resistance, and discuss potential future therapeutic interventions with the goal of specifically eliminating CSCs in a clinical setting.

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Crossref · 10.1038/ncponc1110

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  • Collectively, these studies support a model wherein a pre-existing sub-population of drug-tolerant tumor cells is enriched upon drug treatment, akin to the principle of non-genetic Darwinian selection.

    “Collectively, these studies support a model wherein a pre-existing sub-population of drug-tolerant tumor cells is enriched upon drug treatment, akin to the principle of non-genetic Darwinian selection [60,62,63].”

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References 102 · Cited by 199

Authors
Trumpp, A., & Wiestler, O. D.
Affiliations
  • École Polytechnique Fédérale de Lausanne (CH)
  • German Cancer Research Center (DE)
Corresponding author
Trumpp, Andreas
Venue
Nature Clinical Practice Oncology
Published
2008-04-22
Volume
5
Issue
6
Pages
337-347
ISSN
  • 1743-4254 (ISSN-L)
  • 1743-4262
OpenAlex
W2035704783
Cited by
199
References
102
Citations by year
2026: 2 · 2025: 2 · 2024: 11 · 2023: 5 · 2022: 8 · 2021: 7 · 2020: 10 · 2019: 13 · 2018: 9 · 2017: 10 · 2016: 12 · 2015: 15 · 2014: 10 · 2013: 15 · 2012: 13
FWCI
1.78
Type
journal article
Language
en
Open access
Locations
  • Nature Clinical Practice Oncology (publishedVersion)
  • PubMed (publishedVersion)
  • Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion)
  • Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion, cc-by-nc-nd)
Funders
  • Deutsches Krebsforschungszentrum
  • Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
  • China Scholarship Council
Topics
  • Health Sciences › Medicine › Oncology › Cancer Cells and Metastasis
  • Health Sciences › Medicine › Genetics › Mesenchymal stem cell research
  • Health Sciences › Medicine › Hematology › Hematopoietic Stem Cell Transplantation
Keywords
cancer stem cells, treatment resistance, chemoresistance, radioresistance (biology), self-renewal, tumor recurrence, metastasis, DNA repair, multidrug resistance transporters, hypoxic niche, leukemia, targeted therapy
MeSH terms
Animals, Antineoplastic Agents, Humans, Neoplasms, Neoplastic Stem Cells, Drug Resistance, Neoplasm

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