FOXO3a promotes tumor cell invasion through the induction of matrix metalloproteinases

Peter Storz, Heike Döppler, John A III Copland, Kaylene J. Simpson, Alex Toker

Research output: Contribution to journalArticle

79 Citations (Scopus)

Abstract

The role of the Forkhead transcription factor FOXO3a in processes that promote tumor metastasis is poorly defined. Here, we show that depletion of FOXO3a from cancer cells leads to decreased tumor size specifically due to attenuated invasive migration. During tumor progression, an increase in tumor mass is concomitant with serum deprivation prior to tumor angiogenesis. We show that nuclear retention of FOXO3a due to serum starvation results in greatly increased cancer cell invasion. Exploration of the mechanism by which FOXO3a promotes invasive migration revealed that it induces the expression of matrix metalloproteinase 9 (MMP-9) and MMP-13, both of which have been causally linked to the invasion and progression of numerous human solid tumors. Our results link Forkhead transcription factors to a previously unexplored function in cancer progression by promoting extracellular matrix degradation, allowing tumors to invade neighboring tissues and ultimately metastasize to distant organs.

Original languageEnglish (US)
Pages (from-to)4906-4917
Number of pages12
JournalMolecular and Cellular Biology
Volume29
Issue number18
DOIs
StatePublished - Sep 2009

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Matrix Metalloproteinases
Neoplasms
Forkhead Transcription Factors
Matrix Metalloproteinase 9
Starvation
Serum
Extracellular Matrix
Neoplasm Metastasis

ASJC Scopus subject areas

  • Molecular Biology
  • Cell Biology

Cite this

FOXO3a promotes tumor cell invasion through the induction of matrix metalloproteinases. / Storz, Peter; Döppler, Heike; Copland, John A III; Simpson, Kaylene J.; Toker, Alex.

In: Molecular and Cellular Biology, Vol. 29, No. 18, 09.2009, p. 4906-4917.

Research output: Contribution to journalArticle

Storz, Peter ; Döppler, Heike ; Copland, John A III ; Simpson, Kaylene J. ; Toker, Alex. / FOXO3a promotes tumor cell invasion through the induction of matrix metalloproteinases. In: Molecular and Cellular Biology. 2009 ; Vol. 29, No. 18. pp. 4906-4917.
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