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Localization and characterization of a chromosome 11 tumor suppressor gene using organotypic raft cultures
D Gioeli1, K Conway, B E Weissman
1Curriculum in Toxicology, University of North Carolina at Chapel Hill, 27599, USA.
Abstract:
The development and progression of human cancer often involves the inactivation of tumor suppressor gene function. Alterations in human chromosome 11 during the development of human cutaneous squamous cell carcinoma suggest the presence of a tumor suppressor gene on this chromosome. Moreover, previous studies in our laboratory demonstrated the presence of a functional tumor suppressor gene on chromosome 11 for the human cutaneous squamous cell carcinoma cell line A388.6TG.c2. In this investigation, we have used organotypic culturing of epithelial cells as a novel in vitro assay for tumor suppression. A388.6TG.c2 and control cells form an abnormal stratified epithelium of 8-12 layers when cultivated on organotypic rafts. In contrast, the chromosome 11 microcell hybrids, HMC 100p4B and HMC 100p5A, form an epithelium of only two to three cell layers. This in vitro growth suppression of the chromosome 11 microcell hybrids in the organotypic rafts correlates well with our previous in vivo skin graft experiments. Comparison of the proliferation and apoptotic indices of cell lines grown on the organotypic rafts suggests that the tumor suppressor gene on chromosome 11 has restricted the ability of the microcell hybrids to stratify but has not significantly altered their ability to undergo cell division or programmed cell death. Furthermore, flow cytometric analysis of cells grown on organotypic raft cultures suggests that the chromosome 11 microcell hybrids are actively progressing through the cell cycle rather than arrested in a particular stage. We have used this novel application of organotypic raft cultures to further localize the chromosome 11 tumor suppressor gene. Introduction of a single der(11)t(X;11) chromosome lacking most of the long arm of chromosome 11 into A388.6TG.c2 does not affect growth on organotypic raft cultures. These data suggest the tumor suppressor gene maps to the long arm of chromosome 11 in the region of 11q13-qter.
Insights
A novel organotypic culture assay identified a tumor suppressor gene on chromosome 11. This gene restricts epithelial stratification in cutaneous squamous cell carcinoma cells without affecting cell division or apoptosis.
Area of Science:
- Oncology
- Genetics
- Cell Biology
Background:
- Cancer development involves tumor suppressor gene inactivation.
- Human chromosome 11 alterations are linked to cutaneous squamous cell carcinoma.
- A functional tumor suppressor gene on chromosome 11 was previously identified in the A388.6TG.c2 cell line.
Purpose of the Study:
- To utilize organotypic culturing as an in vitro assay for tumor suppression.
- To investigate the function of the chromosome 11 tumor suppressor gene in epithelial stratification.
- To further localize the tumor suppressor gene on chromosome 11.
Main Methods:
- Organotypic culturing of epithelial cells (A388.6TG.c2 and chromosome 11 microcell hybrids).
- Comparison of epithelial stratification, proliferation, and apoptotic indices.
- Flow cytometric analysis of cell cycle progression.
- Introduction of a der(11)t(X;11) chromosome to map the gene.
Main Results:
- Chromosome 11 microcell hybrids exhibited suppressed epithelial stratification (2-3 layers) compared to controls (8-12 layers) in organotypic cultures.
- The tumor suppressor gene restricted stratification but did not significantly alter cell division or apoptosis.
- Cell cycle analysis indicated active progression, not arrest, in microcell hybrids.
- The tumor suppressor gene was localized to the long arm of chromosome 11 (11q13-qter).
Conclusions:
- Organotypic raft cultures serve as an effective in vitro model for studying tumor suppression.
- The identified chromosome 11 tumor suppressor gene plays a role in regulating epithelial stratification.
- The gene's critical region is mapped to 11q13-qter, providing a target for further research in cutaneous squamous cell carcinoma.