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VHL loss in renal cell carcinoma leads to up-regulation of CUB domain-containing protein 1 to stimulate PKC{delta}-driven migration
- Source :
- Proceedings of the National Academy of Sciences of the United States of America. 108(5)
- Publication Year :
- 2011
-
Abstract
- A common genetic mutation found in clear cell renal cell carcinoma (CC-RCC) is the loss of the von Hippel-Lindau ( VHL ) gene, which results in stabilization of hypoxia-inducible factors (HIFs), and contributes to cancer progression and metastasis. CUB-domain-containing protein 1 (CDCP1) was shown to promote metastasis in scirrhous and lung adenocarcinomas as well as in prostate cancer. In this study, we established a molecular mechanism linking VHL loss to induction of the CDCP1 gene through the HIF-1/2 pathway in renal cancer. Also, we report that Fyn, which forms a complex with CDCP1 and mediates its signaling to PKCδ, is a HIF-1 target gene. Mechanistically, we found that CDCP1 specifically regulates phosphorylation of PKCδ, but not of focal adhesion kinase or Crk-associated substrate. Signal transduction from CDCP1 to PKCδ leads to its activation, increasing migration of CC-RCC. Furthermore, patient survival can be stratified by CDCP1 expression at the cell surface of the tumor. Taken together, our data indicates that CDCP1 protein might serve as a therapeutic target for CC-RCC.
- Subjects :
- Biology
urologic and male genital diseases
Metastasis
Focal adhesion
FYN
Antigens, CD
Antigens, Neoplasm
medicine
Humans
Phosphorylation
Carcinoma, Renal Cell
Multidisciplinary
Cell adhesion molecule
Cancer
Biological Sciences
medicine.disease
female genital diseases and pregnancy complications
Kidney Neoplasms
Neoplasm Proteins
Up-Regulation
Clear cell renal cell carcinoma
Protein Kinase C-delta
Von Hippel-Lindau Tumor Suppressor Protein
Mutation
CDCP1
Cancer research
Signal transduction
Cell Adhesion Molecules
Signal Transduction
Subjects
Details
- ISSN :
- 10916490
- Volume :
- 108
- Issue :
- 5
- Database :
- OpenAIRE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Accession number :
- edsair.doi.dedup.....1be9d3c6b2d86eef410f9d5f154406b7