PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
February 15, 2000Genes & Development834 citationsOpen Access

Loss of PTEN facilitates HIF-1-mediated gene expression

WZWayne ZundelCSCornelia SchindlerDHDaphne A. Haas‐Kogan

Key Points

  • This research investigates how the loss of PTEN affects HIF-1-mediated gene expression in glioblastoma cell lines.
  • Analysis of glioblastoma-derived cell lines with and without functional PTEN.
  • Examined the effects of hypoxia and IGF-1 on gene expression related to angiogenesis.
  • Restored wild-type PTEN to assess changes in HIF-1 activity and related gene expression.
  • Loss of PTEN enhances HIF-1alpha stabilization due to increased Akt activation leading to higher angiogenic gene expression.
  • Restoration of wild-type PTEN decreases hypoxia and IGF-1 induced HIF-1-regulated gene induction.
  • Deregulated Akt activity is linked to tumor expansion in the absence of functional PTEN.

Abstract

In glioblastoma-derived cell lines, PTEN does not significantly alter apoptotic sensitivity or cause complete inhibition of DNA synthesis. However, in these cell lines PTEN regulates hypoxia- and IGF-1-induced angiogenic gene expression by regulating Akt activation of HIF-1 activity. Restoration of wild-type PTEN to glioblastoma cell lines lacking functional PTEN ablates hypoxia and IGF-1 induction of HIF-1-regulated genes. In addition, Akt activation leads to HIF-1alpha stabilization, whereas PTEN attenuates hypoxia-mediated HIF-1alpha stabilization. We propose that loss of PTEN during malignant progression contributes to tumor expansion through the deregulation of Akt activity and HIF-1-regulated gene expression.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Zundel et al. (2000) studied this question.

synapsesocial.com/papers/6a653f1e7d104d3b662f0e6fhttps://doi.org/10.1101/gad.14.4.391
Ask AI
Helpful
Bookmark
Share
View Full Paper