Back to Search
Start Over
Gankyrin activates IL-8 to promote hepatic metastasis of colorectal cancer
- Source :
- Cancer research. 73(14)
- Publication Year :
- 2013
-
Abstract
- Hepatic metastasis is responsible for the majority of colorectal cancer (CRC)-related mortalities. Although Gankyrin (PSMD10) has been implicated in cancer metastasis, its exact role and underlying mechanisms of CRC hepatic metastasis remain largely unknown. Herein, we showed that the expression of Gankyrin was higher in primary CRC with hepatic metastasis compared with CRC without metastasis. RNAi-mediated silencing of Gankyrin expression in highly metastatic human CRC cells impaired their migratory and metastatic capacity in vivo. Genome-wide transcriptome profiling revealed activation of the interleukin (IL)-8 signaling pathway by Gankyrin. Protein levels of IL-8 and cyclin D1 (CCND1), the two important molecules in the IL-8 pathway, were positively correlated with Gankyrin expression in human CRC specimens. Furthermore, genetic deletion of cyclin D1 showed its requirement in Gankyrin-mediated cell migration. Finally, administration of recombinant IL-8 rescued the migratory defect of CRC cells where Gankyrin expression was silenced. Together, our findings highlight the importance of Gankyrin in hepatic metastasis of CRC and point out its candidature as a potential prognostic marker and therapeutic target to improve the clinical management of metastatic CRC. Cancer Res; 73(14); 4548–58. ©2013 AACR.
- Subjects :
- Male
Cancer Research
Proteasome Endopeptidase Complex
Gankyrin
Colorectal cancer
Metastasis
Cell Line
Mice
Cyclin D1
Cell Movement
Proto-Oncogene Proteins
medicine
Gene silencing
Animals
Humans
Neoplasm Invasiveness
Neoplasm Metastasis
neoplasms
biology
Interleukin-8
Liver Neoplasms
Cell migration
3T3 Cells
medicine.disease
digestive system diseases
Mice, Inbred C57BL
HEK293 Cells
Oncology
biology.protein
Cancer research
PSMD10
Signal transduction
Colorectal Neoplasms
Signal Transduction
Subjects
Details
- ISSN :
- 15387445
- Volume :
- 73
- Issue :
- 14
- Database :
- OpenAIRE
- Journal :
- Cancer research
- Accession number :
- edsair.doi.dedup.....4fbd68a693e84e43cef6469138342779