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

被引:37
作者
Aleksic T. [1 ]
Feller S.M. [1 ]
机构
[1] Department of Medical Oncology, Weatherall Institute of Molecular Medicine, Oxford University
关键词
Oxaliplatin; Notch Signalling; DAPT; Platinum Compound; Hes1 Expression;
D O I
10.1186/1478-811X-6-8
中图分类号
学科分类号
摘要
Background: 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§ssup§min §esup§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. Results: 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. Conclusion: 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. 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. © 2008 Aleksic and Feller; licensee BioMed Central Ltd.
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  • [1] Bray S.J., Notch signalling: A simple pathway becomes complex, Nature Reviews Molecular Cell Biology, 7, 9, pp. 678-689, (2006)
  • [2] Fre S., Huyghe M., Mourikis P., Robine S., Louvard D., Artavanis-Tsakonas S., Notch signals control the fate of immature progenitor cells in the intestine, Nature, 435, 7044, pp. 964-968, (2005)
  • [3] Grabher C., Von Boehmer H., Look A.T., Notch 1 activation in the molecular pathogenesis of T-cell acute lymphoblastic leukaemia, Nat Rev Cancer, 6, 5, pp. 347-359, (2006)
  • [4] Radtke F., Clevers H., Self-renewal and cancer of the gut: Two sides of a coin, Science, 307, 5717, pp. 1904-1909, (2005)
  • [5] Van Es J.H., Van Gijn M.E., Riccio O., Van Den Born M., Vooijs M., Begthel H., Cozijnsen M., Robine S., Winton D.J., Radtke F., Clevers H., Notch/γ-secretase inhibition turns proliferative cells in intestinal crypts and adenomas into goblet cells, Nature, 435, 7044, pp. 959-963, (2005)
  • [6] Radtke F., Schweisguth F., Pear W., The Notch 'gospel, EMBO Reports, 6, 12, pp. 1120-1125, (2005)
  • [7] Katoh M., Notch signaling in gastrointestinal tract (review), Int J Oncol, 30, 1, pp. 247-251, (2007)
  • [8] Lai E.C., Notch signaling: Control of cell communication and cell fate, Development, 131, 5, pp. 965-973, (2004)
  • [9] Osipo C., Golde T.E., Osborne B.A., Miele L.A., Off the beaten pathway: The complex cross talk between Notch and NF-kappaB, Lab Invest, 88, 1, pp. 11-17, (2008)
  • [10] Selkoe D., Kopan R., Notch and Presenilin: Regulated intramembrane proteolysis links development and degeneration, Annual Review of Neuroscience, 26, pp. 565-597, (2003)