HIF prolyl hydroxylase-2 inhibition diminishes tumor growth through matrix metalloproteinase-induced TGFβ activation

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

Abstract

A right amount of oxygen and nutrients is essential for a tumor to develop. The role of oxygen dependent pathways and their regulators is therefore of utmost importance although little is known about the detailed impact they can have. Recently we have shown that inhibition of the oxygen sensor PHD2 in tumor cells blocks tumor growth due to the antiproliferative activity of TGFβ. In this study, we refined these results by comparing different shPHD2 sequences in depth in the early phase of tumor growth. Our findings also reveal an intriguing role for MMP2 and MT1MMP in these settings, as these activated proteases display an anti-proliferative characteristic through the activation of downstream TGFβ targets. In conclusion, PHD2 inhibition is essential for the regulation of the anti-tumoral activity in mouse tumor cells and might bring some new insight in our understanding of tumor growth inhibition.

Details

Original languageEnglish
Pages (from-to)216-223
Number of pages8
JournalCancer Biology and Therapy
Volume13
Issue number4
Publication statusPublished - 15 Feb 2012
Peer-reviewedYes

External IDs

PubMed 22354010
ORCID /0000-0002-9467-780X/work/163766687

Keywords

Keywords

  • HIF prolyl hydroxylase-2 (PHD2), Hypoxia, Matrix metalloproteinases, TGFbeta