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Apc10.1: an ApcMin/+ intestinal cell line with retention of heterozygosity
- Source :
- International journal of cancer. 109(2)
- Publication Year :
- 2004
-
Abstract
- APC10.1 is a new intestinal cell line derived from ApcMin/+ mice that retains both the heterozygous Apc genotype and a nonactivated Wnt signaling pathway and displays an early neoplastic phenotype. Although tumorigenic both in immunodepressed and in immunocompetent syngeneic mice, it requires a high cell dose and a long latency. Its epithelial/intestinal origin is shown, in a gene expression profile, by the expression of epithelial transcripts (such as cytokeratin and laminin isoforms) and of developmental regulatory genes (such as Tcf-4, Hnf3beta, p21, Ihh, Hes1) necessary for, or involved in, the maintenance of intestinal stem cells. The lack of activation of the Wnt cascade in APC10.1 cells is shown both by the expression profile of Wnt target genes and by the standard TCF reporter assay. APC10.1 cell line is a novel in vitro model that can contribute to a better understanding of the clinical evolution of familial adenomatous polyposis and to finding of new prophylactic and therapeutic approaches. Supplementary material for this article can be found on the International Journal of Cancer website at http://www.interscience.wiley.com/jpages/0020-7136/suppmat/index.html.
- Subjects :
- Cancer Research
Heterozygote
Genes, APC
Adenomatous polyposis coli
Adenomatous Polyposis Coli Protein
Mice, Nude
Familial adenomatous polyposis
Mice
Proto-Oncogene Proteins
Intestinal Neoplasms
medicine
Tumor Cells, Cultured
Animals
RNA, Neoplasm
HES1
Oligonucleotide Array Sequence Analysis
Reporter gene
biology
Gene Expression Profiling
Wnt signaling pathway
Cell Differentiation
Zebrafish Proteins
medicine.disease
Phenotype
Mice, Inbred C57BL
Wnt Proteins
Cytoskeletal Proteins
Oncology
Adenomatous Polyposis Coli
Cell culture
Immunology
Cancer research
biology.protein
Female
Stem cell
Transcription Factors
Subjects
Details
- ISSN :
- 00207136
- Volume :
- 109
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- International journal of cancer
- Accession number :
- edsair.doi.dedup.....bddfad46094b3b03b60e8b56bd3f7652