Gamma-secretase inhibition combined with platinum compounds enhances cell death in a large subset of colorectal cancer cells

<p>Abstract</p> <p>Background</p> <p>Notch signalling is essential for the development and maintenance of the colonic epithelium. Its inhibition induces a differentiation phenotype in vivo and reduces adenomas in APC<sup>min </sup>mice. Whether Notch signals...

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Main Authors: Feller Stephan M, Aleksic Tamara
Format: Article
Language:English
Published: BMC 2008-10-01
Series:Cell Communication and Signaling
Online Access:http://www.biosignaling.com/content/6/1/8
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spelling doaj-0e7ea79b74df4ba48b507e84c7717a322020-11-24T21:44:41ZengBMCCell Communication and Signaling1478-811X2008-10-0161810.1186/1478-811X-6-8Gamma-secretase inhibition combined with platinum compounds enhances cell death in a large subset of colorectal cancer cellsFeller Stephan MAleksic Tamara<p>Abstract</p> <p>Background</p> <p>Notch signalling is essential for the development and maintenance of the colonic epithelium. Its inhibition induces a differentiation phenotype in vivo and reduces adenomas in APC<sup>min </sup>mice. Whether Notch signals are also required in colorectal cancer (CRC) has remained elusive. Therefore, 64 CRC cell lines were analysed for the occurrence of proteolytically processed, active Notch.</p> <p>Results</p> <p>63 CRC lines contained a fragment with approximately the size of the Notch1 intracellular domain (NICD), which is required for signalling. Subsequent analyses with an antibody that specifically recognises the free Val1744 residue generated by γ-secretase-mediated cleavage of Notch1 showed that a subset of CRC cells lacks this specific Val1744-NICD. Surprisingly, inhibition of Val1744-NICD signalling with different γ-secretase inhibitors (GSI) did not lead to substantial effects on CRC cell line growth or survival. However, transient activation of Erk upon GSI treatment was detected. Since cisplatin relies on Erk activation for bioactivity in some cells, platinum compounds were tested together with GSI and enhanced cell killing in a subset of Val1744-NICD-positive CRC cell lines was detected. Erk inhibition ablated this combination effect.</p> <p>Conclusion</p> <p>We conclude that γ-secretase inhibition results in activation of the MAP kinases Erk1/2 and, when used in conjunction, enhances cell death induced by platinum compounds in a large subset of colorectal cancer cell lines.</p> <p>Furthermore the activation of Erk appears to be of particular importance in mediating the enhanced effect seen, as its inhibition abrogates the observed phenomenon. These findings do not only highlight the importance of signalling pathway crosstalk but they may also suggest a new avenue of combination therapy for some colorectal cancers.</p> http://www.biosignaling.com/content/6/1/8
collection DOAJ
language English
format Article
sources DOAJ
author Feller Stephan M
Aleksic Tamara
spellingShingle Feller Stephan M
Aleksic Tamara
Gamma-secretase inhibition combined with platinum compounds enhances cell death in a large subset of colorectal cancer cells
Cell Communication and Signaling
author_facet Feller Stephan M
Aleksic Tamara
author_sort Feller Stephan M
title Gamma-secretase inhibition combined with platinum compounds enhances cell death in a large subset of colorectal cancer cells
title_short Gamma-secretase inhibition combined with platinum compounds enhances cell death in a large subset of colorectal cancer cells
title_full Gamma-secretase inhibition combined with platinum compounds enhances cell death in a large subset of colorectal cancer cells
title_fullStr Gamma-secretase inhibition combined with platinum compounds enhances cell death in a large subset of colorectal cancer cells
title_full_unstemmed Gamma-secretase inhibition combined with platinum compounds enhances cell death in a large subset of colorectal cancer cells
title_sort gamma-secretase inhibition combined with platinum compounds enhances cell death in a large subset of colorectal cancer cells
publisher BMC
series Cell Communication and Signaling
issn 1478-811X
publishDate 2008-10-01
description <p>Abstract</p> <p>Background</p> <p>Notch signalling is essential for the development and maintenance of the colonic epithelium. Its inhibition induces a differentiation phenotype in vivo and reduces adenomas in APC<sup>min </sup>mice. Whether Notch signals are also required in colorectal cancer (CRC) has remained elusive. Therefore, 64 CRC cell lines were analysed for the occurrence of proteolytically processed, active Notch.</p> <p>Results</p> <p>63 CRC lines contained a fragment with approximately the size of the Notch1 intracellular domain (NICD), which is required for signalling. Subsequent analyses with an antibody that specifically recognises the free Val1744 residue generated by γ-secretase-mediated cleavage of Notch1 showed that a subset of CRC cells lacks this specific Val1744-NICD. Surprisingly, inhibition of Val1744-NICD signalling with different γ-secretase inhibitors (GSI) did not lead to substantial effects on CRC cell line growth or survival. However, transient activation of Erk upon GSI treatment was detected. Since cisplatin relies on Erk activation for bioactivity in some cells, platinum compounds were tested together with GSI and enhanced cell killing in a subset of Val1744-NICD-positive CRC cell lines was detected. Erk inhibition ablated this combination effect.</p> <p>Conclusion</p> <p>We conclude that γ-secretase inhibition results in activation of the MAP kinases Erk1/2 and, when used in conjunction, enhances cell death induced by platinum compounds in a large subset of colorectal cancer cell lines.</p> <p>Furthermore the activation of Erk appears to be of particular importance in mediating the enhanced effect seen, as its inhibition abrogates the observed phenomenon. These findings do not only highlight the importance of signalling pathway crosstalk but they may also suggest a new avenue of combination therapy for some colorectal cancers.</p>
url http://www.biosignaling.com/content/6/1/8
work_keys_str_mv AT fellerstephanm gammasecretaseinhibitioncombinedwithplatinumcompoundsenhancescelldeathinalargesubsetofcolorectalcancercells
AT aleksictamara gammasecretaseinhibitioncombinedwithplatinumcompoundsenhancescelldeathinalargesubsetofcolorectalcancercells
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