Journal
ONCOGENE
Volume 27, Issue 20, Pages 2823-2832Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/sj.onc.1210954
Keywords
phospholipase c gamma 1; rap GEF1; Rap1; adhesion
Funding
- Cancer Research UK Funding Source: Medline
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C gamma 1 (PLC gamma 1) is activated downstream of a variety of extracellular stimuli and has previously been implicated in the regulation of motility responses central to tumour cell invasion. In this study, we used a novel RNAi vector system to achieve conditional PLC gamma 1 knockdown in PC3LN3 human prostate carcinoma cells for further evaluation of PLC gamma 1 in tumour cell biology. Using this approach, we revealed a role for PLC gamma 1 in the regulation of PC3LN3 cell adhesion that appears to be independent of its effects on tumour cell chemotactic migration and spreading in response to extracellular matrix. Subsequent microarray analysis of PLC gamma 1-knockdown cells revealed Rap GEF1 mRNA to be decreased in response to PLC gamma 1 loss. This translated into a decrease in Rap GEF1 protein levels and a significant loss of Rap1 activity in PLC gamma 1-knockdown cells. Transient knockdown of Rap GEF1 caused a reduction in PC3LN3 adhesion while overexpression of Rap GEF1 rescued the PLC gamma 1 knockdown-induced adhesion defect. These data highlight control of the Rap GEF1-Rap1 molecular switch as a specific requirement for PLC gamma 1-mediated tumour cell adhesion.
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