Isolation of head and neck squamous carcinoma cancer stem-like cells in a syngeneic mouse model and analysis of hypoxia effect
0301 basic medicine
MESH: Tumor Burden
MESH: Cell Line, Tumor
MESH: Gene Expression
MESH: Cell Hypoxia
MESH: Retinal Dehydrogenase
MESH: Spheroids, Cellular
Gene Expression
MESH: Flow Cytometry
Aldehyde Dehydrogenase 1 Family
Mice
03 medical and health sciences
MESH: Cell Proliferation
Cell Line, Tumor
Spheroids, Cellular
Animals
MESH: Animals
[SDV.BBM]Life Sciences [q-bio]/Biochemistry, Molecular Biology
MESH: Mice, Inbred C3H
MESH: Mice
Cell Proliferation
Mice, Inbred C3H
Retinal Dehydrogenase
MESH: Carcinoma, Squamous Cell
Flow Cytometry
MESH: Neoplastic Stem Cells
Cell Hypoxia
Tumor Burden
3. Good health
MESH: Head and Neck Neoplasms
Isoenzymes
Transplantation, Isogeneic
Head and Neck Neoplasms
MESH: Isoenzymes
Carcinoma, Squamous Cell
Neoplastic Stem Cells
Female
MESH: Transplantation, Isogeneic
MESH: Female
MESH: Neoplasm Transplantation
Neoplasm Transplantation
DOI:
10.3892/or.2012.1904
Publication Date:
2012-07-06T08:32:05Z
AUTHORS (8)
ABSTRACT
The incidence of oral tumors is increasing around the world and despite recent advances in early detection and diagnosis, current treatments are still unsatisfactory. Recent data suggest that tumor persistence and recurrence could be due to the presence of a rare cell population called cancer stem cells (CSCs), which are generally spared by traditional treatments. Therefore, identification and characterization of CSCs are extremely important to develop novel and effective treatment strategies for cancer. The aim of this study was to identify and isolate CSCs in an established murine head and neck squamous cell carcinoma (HNSCC) cell line and to investigate the influence of hypoxic conditions on the isolated cell popul-ation. Using the expression of the aldehyde dehydrogenase 1 (ALDH1) enzymatic activity, which is now recognized as a CSC marker in various tumors, we isolated a cell population expressing high levels of ALDH1 (ALDH1high) representing 1±0.6% in the murine SCC-VII cell line. These cells were injected subcutaneously in syngeneic animals to evaluate their tumorigenic properties. For the lowest injected cell dose (250 injected cells), tumor occurrence and median tumor size were higher in ALDH1high injected mice than in ALDH1low injected mice. Following an in vivo passage and culture in serum-free medium, the percentage of ALDH1high cells increased by 3‑fold in SCC-VII CSCs (oral spheres) compared to the SCC-VII cell line. This percentage was further increased when oral spheres were cultured under hypoxic conditions. In conclusion, this study reports for the first time the isolation of HNSCC CSCs in a syngeneic mouse model and the use of hypoxia as a method to further enrich the ALDH1high cell population.
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