Accession Number:

ADA612330

Title:

Studying the Role of Eukaryotic Translation Initiation Factor 4E (eIF4E) Phosphorylation by MNK1/2 Kinases in Prostate Cancer Development and Progression

Descriptive Note:

Annual rept. 1 Jun 2010-31 May 2013

Corporate Author:

MCGILL UNIV MONTREAL (CANADA)

Personal Author(s):

Report Date:

2013-06-01

Pagination or Media Count:

14.0

Abstract:

The mRNA cap-binding protein eukaryotic initiation factor 4E eIF4E plays a key role in cancer progression. We have recently shown Furic et al., 2010 that phosphorylation of eIF4E at Ser209 by the MNK family of kinases promotes prostate cancer progression in a mouse model bearing a tissue-specific conditional PTEN deletion in prostatic epithelia. The mechanism whereby eIF4E phosphorylation promotes prostate cancer development remains unexplored. Genome-wide analysis studies by our group Furic et al. 2010 had shown that phosphorylation of eIF4E regulated the protein levels of a large number of proteins linked to remodeling of the tissue surrounding the tumor. Of note, the levels of MMP3, a matrix metalloprotease required for epithelia-mesenchymal transition EMT, is decreased in eIF4E S209A knockin mouse embryo fibroblasts. In a logical continuity of this finding, next we investigated whether eIF4E phosphorylation is a determinant factor in metastatic progression. The ability of eIF4E to promote metastasis in various mouse models and its association with poor prognosis in the clinic is well documented De Benedetti et al., 2004 Nasr et al., 2013 Pettersson et al., 2011 Graff et al., 2009, but the mechanism by which phospho-eIF4E may promote metastasis is unknown. In this final report, we elucidate a mechanism by which eIF4E phosphorylation drives metastatic progression. Specifically, we show that phosphorylation of eIF4E promotes the translation of Snail2 and MMP3, both key factors in epithelia-mesenchymal transition during metastasis. Our most recent findings yield important information for a better understanding of how phosphorylation of the proto-oncogene eIF4E drives cancer progression.

Subject Categories:

  • Biochemistry
  • Medicine and Medical Research

Distribution Statement:

APPROVED FOR PUBLIC RELEASE