Cargando…
Substituted titanocenes induce caspase-dependent apoptosis in human epidermoid carcinoma cells in vitro and exhibit antitumour activity in vivo
Titanocene compounds are a novel series of agents that exhibit cytotoxic effects in a variety of human cancer cells in vitro and in vivo. In this study, the antiproliferative activity of two titanocenes (Titanocenes X and Y) was evaluated in human epidermoid cancer cells in vitro. Titanocenes X and...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2007
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360460/ https://www.ncbi.nlm.nih.gov/pubmed/17923871 http://dx.doi.org/10.1038/sj.bjc.6604021 |
_version_ | 1782153054983815168 |
---|---|
author | Bannon, J H Fichtner, I O'Neill, A Pampillón, C Sweeney, N J Strohfeldt, K Watson, R W Tacke, M Mc Gee, M M |
author_facet | Bannon, J H Fichtner, I O'Neill, A Pampillón, C Sweeney, N J Strohfeldt, K Watson, R W Tacke, M Mc Gee, M M |
author_sort | Bannon, J H |
collection | PubMed |
description | Titanocene compounds are a novel series of agents that exhibit cytotoxic effects in a variety of human cancer cells in vitro and in vivo. In this study, the antiproliferative activity of two titanocenes (Titanocenes X and Y) was evaluated in human epidermoid cancer cells in vitro. Titanocenes X and Y induce apoptotic cell death in epidermoid cancer cells, with IC50 values that are comparable to cisplatin. Characterisation of the cell death pathway induced by titanocene compounds in A431 cells revealed that apoptosis is preceded by cell cycle arrest and the inhibition of cell proliferation. The induction of apoptosis is dependent on the activation of caspase-3 and -7 but not caspase-8. Furthermore, the antitumour activity of Titanocene Y was tested in an A431 xenograft model of epidermoid cancer. Results indicate that Titanocene Y significantly reduced the growth of A431 xenografts with an antitumour effect similar to cisplatin. These results suggest that titanocenes represent a novel series of promising antitumour agents. |
format | Text |
id | pubmed-2360460 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23604602009-09-10 Substituted titanocenes induce caspase-dependent apoptosis in human epidermoid carcinoma cells in vitro and exhibit antitumour activity in vivo Bannon, J H Fichtner, I O'Neill, A Pampillón, C Sweeney, N J Strohfeldt, K Watson, R W Tacke, M Mc Gee, M M Br J Cancer Translational Therapeutics Titanocene compounds are a novel series of agents that exhibit cytotoxic effects in a variety of human cancer cells in vitro and in vivo. In this study, the antiproliferative activity of two titanocenes (Titanocenes X and Y) was evaluated in human epidermoid cancer cells in vitro. Titanocenes X and Y induce apoptotic cell death in epidermoid cancer cells, with IC50 values that are comparable to cisplatin. Characterisation of the cell death pathway induced by titanocene compounds in A431 cells revealed that apoptosis is preceded by cell cycle arrest and the inhibition of cell proliferation. The induction of apoptosis is dependent on the activation of caspase-3 and -7 but not caspase-8. Furthermore, the antitumour activity of Titanocene Y was tested in an A431 xenograft model of epidermoid cancer. Results indicate that Titanocene Y significantly reduced the growth of A431 xenografts with an antitumour effect similar to cisplatin. These results suggest that titanocenes represent a novel series of promising antitumour agents. Nature Publishing Group 2007-11-05 2007-10-09 /pmc/articles/PMC2360460/ /pubmed/17923871 http://dx.doi.org/10.1038/sj.bjc.6604021 Text en Copyright © 2007 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Translational Therapeutics Bannon, J H Fichtner, I O'Neill, A Pampillón, C Sweeney, N J Strohfeldt, K Watson, R W Tacke, M Mc Gee, M M Substituted titanocenes induce caspase-dependent apoptosis in human epidermoid carcinoma cells in vitro and exhibit antitumour activity in vivo |
title | Substituted titanocenes induce caspase-dependent apoptosis in human epidermoid carcinoma cells in vitro and exhibit antitumour activity in vivo |
title_full | Substituted titanocenes induce caspase-dependent apoptosis in human epidermoid carcinoma cells in vitro and exhibit antitumour activity in vivo |
title_fullStr | Substituted titanocenes induce caspase-dependent apoptosis in human epidermoid carcinoma cells in vitro and exhibit antitumour activity in vivo |
title_full_unstemmed | Substituted titanocenes induce caspase-dependent apoptosis in human epidermoid carcinoma cells in vitro and exhibit antitumour activity in vivo |
title_short | Substituted titanocenes induce caspase-dependent apoptosis in human epidermoid carcinoma cells in vitro and exhibit antitumour activity in vivo |
title_sort | substituted titanocenes induce caspase-dependent apoptosis in human epidermoid carcinoma cells in vitro and exhibit antitumour activity in vivo |
topic | Translational Therapeutics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360460/ https://www.ncbi.nlm.nih.gov/pubmed/17923871 http://dx.doi.org/10.1038/sj.bjc.6604021 |
work_keys_str_mv | AT bannonjh substitutedtitanocenesinducecaspasedependentapoptosisinhumanepidermoidcarcinomacellsinvitroandexhibitantitumouractivityinvivo AT fichtneri substitutedtitanocenesinducecaspasedependentapoptosisinhumanepidermoidcarcinomacellsinvitroandexhibitantitumouractivityinvivo AT oneilla substitutedtitanocenesinducecaspasedependentapoptosisinhumanepidermoidcarcinomacellsinvitroandexhibitantitumouractivityinvivo AT pampillonc substitutedtitanocenesinducecaspasedependentapoptosisinhumanepidermoidcarcinomacellsinvitroandexhibitantitumouractivityinvivo AT sweeneynj substitutedtitanocenesinducecaspasedependentapoptosisinhumanepidermoidcarcinomacellsinvitroandexhibitantitumouractivityinvivo AT strohfeldtk substitutedtitanocenesinducecaspasedependentapoptosisinhumanepidermoidcarcinomacellsinvitroandexhibitantitumouractivityinvivo AT watsonrw substitutedtitanocenesinducecaspasedependentapoptosisinhumanepidermoidcarcinomacellsinvitroandexhibitantitumouractivityinvivo AT tackem substitutedtitanocenesinducecaspasedependentapoptosisinhumanepidermoidcarcinomacellsinvitroandexhibitantitumouractivityinvivo AT mcgeemm substitutedtitanocenesinducecaspasedependentapoptosisinhumanepidermoidcarcinomacellsinvitroandexhibitantitumouractivityinvivo |