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Coiled-coil domain containing 68 (CCDC68) demonstrates a tumor suppressive role in pancreatic ductal adenocarcinoma
- Source :
- Oncogene
- Publication Year :
- 2014
-
Abstract
- Using integrative genomics and functional screening we identified coiled-coil domain containing 68 (CCDC68) as a novel putative tumor suppressor (TSG) in pancreatic ductal adenocarcinoma (PDAC). CCDC68 allelic losses were documented in 48% of primary PDAC patient tumors, 50% of PDAC cell lines, and 30% of primary patient derived xenografts. We also discovered a SNP variant (SNP rs1344011) that leads to exon skipping and generation of an unstable protein isoform CCDC68Δ69–114 in 31% of PDAC patients. Overexpression of full length CCDC68 (CCDC68wt) in PANC-1 and Hs.766T PDAC cell lines lacking CDCC68 expression decreased proliferation and tumorigenicity in scid mice. In contrast, downregulation of endogenous CCDC68 in MIAPaca-2 cells increased tumor growth rate. These effects were not observed with the deletion-containing isoform, CCDC68Δ69–114. In conclusion, our results suggest that CCDC68 is a novel candidate TSG in PDAC.
- Subjects :
- Gene isoform
Cancer Research
Tumor suppressor gene
endocrine system diseases
tumor suppressor
Transplantation, Heterologous
Mice, SCID
Biology
Polymorphism, Single Nucleotide
Article
integrative genomics
alternative splicing
Downregulation and upregulation
RNA interference
Cell Line, Tumor
CCDC68
Genetics
pancreatic adenocarcinoma
Animals
Humans
Protein Isoforms
primary patient xenograft models
Molecular Biology
In Situ Hybridization, Fluorescence
Cell Proliferation
Cell growth
Reverse Transcriptase Polymerase Chain Reaction
Tumor Suppressor Proteins
Immunohistochemistry
Exon skipping
digestive system diseases
3. Good health
Tumor Burden
Gene Expression Regulation, Neoplastic
Pancreatic Neoplasms
Cell culture
MAPK signalling
Mutation
Cancer research
RNA Interference
Carcinoma, Pancreatic Ductal
Subjects
Details
- Language :
- English
- ISSN :
- 14765594 and 09509232
- Volume :
- 34
- Issue :
- 32
- Database :
- OpenAIRE
- Journal :
- Oncogene
- Accession number :
- edsair.doi.dedup.....fc921419de2b075639c67396a91a285b