Abstract 3036: The dependence receptor TrkC is a putative colon cancer tumor suppressor

Backgrounds & Aims: The TrkC neurotrophin receptor belongs to the functional dependence receptors family, members of which share the ability to induce apoptosis in the absence of their ligands. Such a trait has been hypothesized to confer tumor-suppressor activity. Indeed, cells that express the...

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Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 2013-04, Vol.73 (8_Supplement), p.3036-3036
Hauptverfasser: Genevois, Anne-Laure, Ichim, Gabriel, Coissieux, Marie-May, Lambert, Marie-Pierre, Lepinasse, Florian, Herceg, Zdenko, Scoazec, Jean-Yves, Tauszig-Delamasure, Servane, Mehlen, Patrick
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Zusammenfassung:Backgrounds & Aims: The TrkC neurotrophin receptor belongs to the functional dependence receptors family, members of which share the ability to induce apoptosis in the absence of their ligands. Such a trait has been hypothesized to confer tumor-suppressor activity. Indeed, cells that express these receptors are thought to be dependent on ligand availability for their survival, a mechanism that inhibits uncontrolled tumor cell proliferation and migration. TrkC is yet a relatively classic tyrosine kinase receptor and therefore generally rather considered as a proto-oncogene. We investigated here whether, because of its dependence receptor activity, TrkC is a putative tumor suppressor in colorectal malignancies. Methods: The level of TrkC was analyzed in a panel of 45 primary sporadic colorectal carcinomas. Loss of heterozygosity and epigenetic alterations in the TrkC promoter were also analyzed. The level of TrkC was also analyzed in a panel of colorectal cancer cell lines. The TrkC tumor suppressive activity was investigated by expressing TrkC and related TrkC variants in colorectal cancer cell lines and by measuring apoptosis, anchorage-independent growth, migration and tumor growth in a chicken model. Results: We show here that TrkC expression is down-regulated in a large fraction of human colorectal cancers, mainly through promoter methylation. Moreover, we show that TrkC silencing by promoter methylation is a selective advantage for colorectal cell lines to limit tumor cell death. Consequently, we show that reestablished TrkC expression in colorectal cancer cell lines is associated with tumor cell death and inhibition of in vitro characteristics of cell transformation and in vivo tumor growth. Conclusions: The loss of TrkC expression observed in human colorectal cancer is a selective advantage for tumor cell survival. Thus, TrkC appears to be a putative new colon cancer tumor suppressor. Citation Format: Anne-Laure Genevois, Gabriel Ichim, Marie-May Coissieux, Marie-Pierre Lambert, Florian Lepinasse, Zdenko Herceg, Jean-Yves Scoazec, Servane Tauszig-Delamasure, Patrick Mehlen. The dependence receptor TrkC is a putative colon cancer tumor suppressor. [abstract]. In: Proceedings of the 104th Annual Meeting of the American Association for Cancer Research; 2013 Apr 6-10; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2013;73(8 Suppl):Abstract nr 3036. doi:10.1158/1538-7445.AM2013-3036
ISSN:0008-5472
1538-7445
DOI:10.1158/1538-7445.AM2013-3036