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In vitro chemosensitivity of head and neck cancer cell lines

BACKGROUND: Systemic treatment of head and neck squamous cell carcinoma (HNSCC) includes a variety of antineoplastic drugs. However, drug-resistance interferes with the effectiveness of chemotherapy. Preclinical testing models are needed in order to develop approaches to overcome chemoresistance. ME...

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Autores principales: Schuler, PJ, Trellakis, S, Greve, J, Bas, M, Bergmann, C, Bölke, E, Lehnerdt, G, Mattheis, S, Albers, AE, Brandau, S, Lang, S, Whiteside, TL, Bier, H, Hoffmann, TK
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458702/
https://www.ncbi.nlm.nih.gov/pubmed/20947470
http://dx.doi.org/10.1186/2047-783X-15-8-337
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author Schuler, PJ
Trellakis, S
Greve, J
Bas, M
Bergmann, C
Bölke, E
Lehnerdt, G
Mattheis, S
Albers, AE
Brandau, S
Lang, S
Whiteside, TL
Bier, H
Hoffmann, TK
author_facet Schuler, PJ
Trellakis, S
Greve, J
Bas, M
Bergmann, C
Bölke, E
Lehnerdt, G
Mattheis, S
Albers, AE
Brandau, S
Lang, S
Whiteside, TL
Bier, H
Hoffmann, TK
author_sort Schuler, PJ
collection PubMed
description BACKGROUND: Systemic treatment of head and neck squamous cell carcinoma (HNSCC) includes a variety of antineoplastic drugs. However, drug-resistance interferes with the effectiveness of chemotherapy. Preclinical testing models are needed in order to develop approaches to overcome chemoresistance. METHODS: Ten human cell lines were obtained from HNSCC, including one with experimentally-induced cisplatin resistance. Inhibition of cell growth by seven chemotherapeutic agents (cisplatin, carboplatin, 5- fluorouracil, methotrexate, bleomycin, vincristin, and paclitaxel) was measured using metabolic MTT-uptake assay and correlated to clinically-achievable plasma concentrations. RESULTS: All drugs inhibited cell growth in a concentration-dependent manner with an IC50 comparable to that achievable in vivo. However, response curves for methotrexate were unsatisfactory and for paclitaxel, the solubilizer cremophor EL was toxic. Cross-resistance was observed between cisplatin and carboplatin. CONCLUSION: Chemosensitivity of HNSCC cell lines can be determined using the MTT-uptake assay. For DNA-interfering cytostatics and vinca alkaloids this is a simple and reproducible procedure. Determined in vitro chemosensitivity serves as a baseline for further experimental approaches aiming to modulate chemoresistance in HNSCC with potential clinical significance.
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spelling pubmed-34587022012-09-27 In vitro chemosensitivity of head and neck cancer cell lines Schuler, PJ Trellakis, S Greve, J Bas, M Bergmann, C Bölke, E Lehnerdt, G Mattheis, S Albers, AE Brandau, S Lang, S Whiteside, TL Bier, H Hoffmann, TK Eur J Med Res Research BACKGROUND: Systemic treatment of head and neck squamous cell carcinoma (HNSCC) includes a variety of antineoplastic drugs. However, drug-resistance interferes with the effectiveness of chemotherapy. Preclinical testing models are needed in order to develop approaches to overcome chemoresistance. METHODS: Ten human cell lines were obtained from HNSCC, including one with experimentally-induced cisplatin resistance. Inhibition of cell growth by seven chemotherapeutic agents (cisplatin, carboplatin, 5- fluorouracil, methotrexate, bleomycin, vincristin, and paclitaxel) was measured using metabolic MTT-uptake assay and correlated to clinically-achievable plasma concentrations. RESULTS: All drugs inhibited cell growth in a concentration-dependent manner with an IC50 comparable to that achievable in vivo. However, response curves for methotrexate were unsatisfactory and for paclitaxel, the solubilizer cremophor EL was toxic. Cross-resistance was observed between cisplatin and carboplatin. CONCLUSION: Chemosensitivity of HNSCC cell lines can be determined using the MTT-uptake assay. For DNA-interfering cytostatics and vinca alkaloids this is a simple and reproducible procedure. Determined in vitro chemosensitivity serves as a baseline for further experimental approaches aiming to modulate chemoresistance in HNSCC with potential clinical significance. BioMed Central 2010-08-20 /pmc/articles/PMC3458702/ /pubmed/20947470 http://dx.doi.org/10.1186/2047-783X-15-8-337 Text en Copyright ©2010 I. Holzapfel Publishers
spellingShingle Research
Schuler, PJ
Trellakis, S
Greve, J
Bas, M
Bergmann, C
Bölke, E
Lehnerdt, G
Mattheis, S
Albers, AE
Brandau, S
Lang, S
Whiteside, TL
Bier, H
Hoffmann, TK
In vitro chemosensitivity of head and neck cancer cell lines
title In vitro chemosensitivity of head and neck cancer cell lines
title_full In vitro chemosensitivity of head and neck cancer cell lines
title_fullStr In vitro chemosensitivity of head and neck cancer cell lines
title_full_unstemmed In vitro chemosensitivity of head and neck cancer cell lines
title_short In vitro chemosensitivity of head and neck cancer cell lines
title_sort in vitro chemosensitivity of head and neck cancer cell lines
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458702/
https://www.ncbi.nlm.nih.gov/pubmed/20947470
http://dx.doi.org/10.1186/2047-783X-15-8-337
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