Mechanisms of Disease: Cancer stem cells--targeting the evil twin
Open accessAbstract
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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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].”
From Emerging Insights into Targeted Therapy-Tolerant Persister Cells in Cancer (2021) · cites this paper as [62]
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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
- ORCID
- 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
- green
- infoscience.epfl.ch
- Licence
- www.springer.com/tdm (tdm)
- 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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