HIF prolyl hydroxylase-2 inhibition diminishes tumor growth through matrix metalloproteinase-induced TGFβ activation
Research output: Contribution to journal › Research article › Contributed › peer-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 language | English |
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Pages (from-to) | 216-223 |
Number of pages | 8 |
Journal | Cancer Biology and Therapy |
Volume | 13 |
Issue number | 4 |
Publication status | Published - 15 Feb 2012 |
Peer-reviewed | Yes |
External IDs
PubMed | 22354010 |
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ORCID | /0000-0002-9467-780X/work/163766687 |
Keywords
ASJC Scopus subject areas
Keywords
- HIF prolyl hydroxylase-2 (PHD2), Hypoxia, Matrix metalloproteinases, TGFbeta