Heat shock protein Hsp72 plays an essential role in Her2-induced mammary tumorigenesis

L. Meng, C. Hunt, J. A. Yaglom, V. L. Gabai, M. Y. Sherman

Research output: Contribution to journalArticlepeer-review

62 Scopus citations

Abstract

The major heat shock protein Hsp72 is expressed at elevated levels in many human cancers and its expression correlates with tumor progression. Here, we investigated the role of Hsp72 in Her2 oncogene-induced neoplastic transformation and tumorigenesis. Expression of Her2 in untransformed MCF10A mammary epithelial cells caused transformation, as judged by foci formation in culture and tumorigenesis in xenografts. However, expression of Her2 in Hsp72-depleted cells failed to induce transformation. The anti-tumorigenic effects of Hsp72 downregulation were associated with cellular senescence because of accumulation of p21 and depletion of survivin. Accordingly, either knockdown of p21 or expression of survivin reversed this senescence process. Further, we developed an animal model of Hsp72-dependent breast cancer associated with expression of Her2. Knockout (KO) of Hsp72 almost completely suppressed tumorigenesis in the MMTVneu breast cancer mouse model. In young Hsp72 KO mice, expression of Her2 instead of mammary tissue hyperplasia led to suppression of duct development and blocked alveolar budding. These effects were due to massive cell senescence in mammary tissue, which was associated with upregulation of p21 and downregulation of survivin. Therefore, Hsp72 has an essential role in Her2-induced tumorigenesis by regulating oncogene-induced senescence pathways.

Original languageEnglish (US)
Pages (from-to)2836-2845
Number of pages10
JournalOncogene
Volume30
Issue number25
DOIs
StatePublished - Jun 23 2011

Keywords

  • HER2
  • Hsp72
  • p21
  • senescence
  • survivin

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cancer Research

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