Abstract |
Cancer stem-like cells (CSCs)/tumor-initiating cells ( TICs) are a small population of cancer cells that have the properties of tumor-initiating ability, self-renewal and differentiation. These properties suggest that CSCs/ TICs are essential for tumor maintenance, recurrence and distant metastasis. Thus, elimination of CSCs/ TICs is essential to cure malignant diseases. However, there are several studies reporting that CSCs/ TICs are more resistant to standard cancer therapies, including chemotherapy and radiotherapy, than non-CSC/ TIC populations. How then, can we eliminate CSCs/ TICs? Immunotherapy might be the possible answer. In recent analysis, innate immunity (natural killer cells and gammadeltaT cells) and also adaptive immunity (cytotoxic T lymphocyte-based cellular immunity and antibody-based humoral immunity) can recognize CSCs/ TICs in vitro efficiently. Furthermore, CSC/ TIC-specific monoclonal antibody therapies are also efficient in vivo. In this article, we describe the potency, possibilities and problems of CSC/ TIC-targeting immunotherapy.
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Authors | Yoshihiko Hirohashi, Toshihiko Torigoe, Satoko Inoda, Akari Takahashi, Rena Morita, Satoshi Nishizawa, Yasuaki Tamura, Hiromu Suzuki, Minoru Toyota, Noriyuki Sato |
Journal | Immunotherapy
(Immunotherapy)
Vol. 2
Issue 2
Pg. 201-11
(Mar 2010)
ISSN: 1750-7448 [Electronic] England |
PMID | 20635928
(Publication Type: Journal Article, Review)
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Chemical References |
- Antibodies, Neoplasm
- Antigens, Neoplasm
- Antigens, Surface
- Biomarkers, Tumor
- Isoenzymes
- Aldehyde Dehydrogenase 1 Family
- Aldehyde Dehydrogenase
- ALDH1A1 protein, human
- Retinal Dehydrogenase
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Topics |
- Adaptive Immunity
- Aldehyde Dehydrogenase
(analysis)
- Aldehyde Dehydrogenase 1 Family
- Antibodies, Neoplasm
(immunology)
- Antigens, Neoplasm
(immunology)
- Antigens, Surface
(immunology)
- Biomarkers, Tumor
(analysis)
- Feasibility Studies
- Forecasting
- Humans
- Immunity, Innate
- Immunotherapy
(methods)
- Isoenzymes
(analysis)
- Killer Cells, Natural
(immunology)
- Models, Biological
- Neoplasms
(immunology, therapy)
- Neoplastic Stem Cells
(chemistry, immunology)
- Retinal Dehydrogenase
- T-Lymphocyte Subsets
(immunology)
- T-Lymphocytes, Cytotoxic
(immunology)
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