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Effects of small interfering RNA targeting thymidylate synthase on survival of ACC3 cells from salivary adenoid cystic carcinoma
BACKGROUND: Thymidylate synthase (TS) is an important target for chemotherapeutic treatment of cancer and high expression of TS has been associated with poor prognosis or refractory disease in several cancers including colorectal and head and neck cancer. Although TS is known to regulate cell cycles...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2628925/ https://www.ncbi.nlm.nih.gov/pubmed/19036131 http://dx.doi.org/10.1186/1471-2407-8-348 |
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author | Shirasaki, Takashi Maruya, Shin-ichiro Mizukami, Hiroki Kakehata, Seiji Kurotaki, Hidekachi Yagihashi, Soroku Shinkawa, Hideichi |
author_facet | Shirasaki, Takashi Maruya, Shin-ichiro Mizukami, Hiroki Kakehata, Seiji Kurotaki, Hidekachi Yagihashi, Soroku Shinkawa, Hideichi |
author_sort | Shirasaki, Takashi |
collection | PubMed |
description | BACKGROUND: Thymidylate synthase (TS) is an important target for chemotherapeutic treatment of cancer and high expression of TS has been associated with poor prognosis or refractory disease in several cancers including colorectal and head and neck cancer. Although TS is known to regulate cell cycles and transcription factors, its potency as a therapeutic target has not been fully explored in adenoid cystic carcinoma (ACC). METHODS: An ACC cell line (ACC3) was transfected with siRNA targeting the TS gene and inhibition of cell growth and induction of apoptosis-associated molecules were evaluated in vitro. In addition, the in vivo effect of TS siRNA on tumor progression was assessed using a xenograft model. RESULTS: Our results demonstrated that ACC3 cells showed significantly higher TS expression than non-cancer cell lines and the induction of TS siRNA led to inhibition of cell proliferation. The effect was associated with an increase in p53, p21, and active caspase-3 and S-phase accumulation. We also found up-regulation of spermidine/spermine N1-acetyltransferase (SSAT), a polyamine metabolic enzyme. Furthermore, treatment with TS siRNA delivered by atelocollagen showed a significant cytostatic effect through the induction of apoptosis in a xenograft model. CONCLUSION: TS may be an important therapeutic target and siRNA targeting TS may be of potential therapeutic value in ACC. |
format | Text |
id | pubmed-2628925 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26289252009-01-21 Effects of small interfering RNA targeting thymidylate synthase on survival of ACC3 cells from salivary adenoid cystic carcinoma Shirasaki, Takashi Maruya, Shin-ichiro Mizukami, Hiroki Kakehata, Seiji Kurotaki, Hidekachi Yagihashi, Soroku Shinkawa, Hideichi BMC Cancer Research Article BACKGROUND: Thymidylate synthase (TS) is an important target for chemotherapeutic treatment of cancer and high expression of TS has been associated with poor prognosis or refractory disease in several cancers including colorectal and head and neck cancer. Although TS is known to regulate cell cycles and transcription factors, its potency as a therapeutic target has not been fully explored in adenoid cystic carcinoma (ACC). METHODS: An ACC cell line (ACC3) was transfected with siRNA targeting the TS gene and inhibition of cell growth and induction of apoptosis-associated molecules were evaluated in vitro. In addition, the in vivo effect of TS siRNA on tumor progression was assessed using a xenograft model. RESULTS: Our results demonstrated that ACC3 cells showed significantly higher TS expression than non-cancer cell lines and the induction of TS siRNA led to inhibition of cell proliferation. The effect was associated with an increase in p53, p21, and active caspase-3 and S-phase accumulation. We also found up-regulation of spermidine/spermine N1-acetyltransferase (SSAT), a polyamine metabolic enzyme. Furthermore, treatment with TS siRNA delivered by atelocollagen showed a significant cytostatic effect through the induction of apoptosis in a xenograft model. CONCLUSION: TS may be an important therapeutic target and siRNA targeting TS may be of potential therapeutic value in ACC. BioMed Central 2008-11-26 /pmc/articles/PMC2628925/ /pubmed/19036131 http://dx.doi.org/10.1186/1471-2407-8-348 Text en Copyright © 2008 Shirasaki et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Shirasaki, Takashi Maruya, Shin-ichiro Mizukami, Hiroki Kakehata, Seiji Kurotaki, Hidekachi Yagihashi, Soroku Shinkawa, Hideichi Effects of small interfering RNA targeting thymidylate synthase on survival of ACC3 cells from salivary adenoid cystic carcinoma |
title | Effects of small interfering RNA targeting thymidylate synthase on survival of ACC3 cells from salivary adenoid cystic carcinoma |
title_full | Effects of small interfering RNA targeting thymidylate synthase on survival of ACC3 cells from salivary adenoid cystic carcinoma |
title_fullStr | Effects of small interfering RNA targeting thymidylate synthase on survival of ACC3 cells from salivary adenoid cystic carcinoma |
title_full_unstemmed | Effects of small interfering RNA targeting thymidylate synthase on survival of ACC3 cells from salivary adenoid cystic carcinoma |
title_short | Effects of small interfering RNA targeting thymidylate synthase on survival of ACC3 cells from salivary adenoid cystic carcinoma |
title_sort | effects of small interfering rna targeting thymidylate synthase on survival of acc3 cells from salivary adenoid cystic carcinoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2628925/ https://www.ncbi.nlm.nih.gov/pubmed/19036131 http://dx.doi.org/10.1186/1471-2407-8-348 |
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