An absence of stromal caveolin-1 is associated with advanced prostate cancer, metastatic disease and epithelial Akt activation

Dolores Di Vizio, Matteo Morello, Federica Sotgia, Richard G. Pestell, Michael R. Freeman, Michael P. Lisanti

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Here, we examined the status of stromal Cav-1 expression in patients with benign prostatic hypertrophy (BPH), primary prostate cancers (PCa), and prostate-cancer metastases (Mets). Interestingly, an absence of stromal Cav-1 directly correlated with prostate cancer disease progression. For example, virtually all BPH samples showed abundant stromal Cav-1 immunostaining. In contrast, in a subset of patients with primary prostate cancer, the stromal levels of Cav-1 were significantly decreased, and this correlated with a high Gleason score, indicative of a worse prognosis and poor clinical outcome. Remarkably, all metastatic tumors (either from lymph node or bone) were completely negative for stromal Cav-1 staining. Thus, stromal Cav-1 expression may be considered as a new biomarker of prostate cancer disease progression and metastasis. Mechanistically, stromal Cav-1 levels were inversely correlated with the epithelial expression levels of Cav-1 and epithelial phospho-Akt. Thus, loss of stromal Cav-1 is predictive of elevated levels of epithelial Cav-1 and epithelial Akt-activation. This provides important new clinical evidence for paracrine signaling between prostate cancer epithelial cells and the tumor stromal micro-environment, especially related to disease progression and metastasis. ©2009 Landes Bioscience.
    Original languageEnglish
    Pages (from-to)2420-2424
    Number of pages4
    JournalCell Cycle
    Volume8
    Issue number15
    Publication statusPublished - 1 Aug 2009

    Keywords

    • Akt signaling
    • Caveolin-1
    • Metastasis
    • Prostate cancer
    • Tumor progression

    Fingerprint

    Dive into the research topics of 'An absence of stromal caveolin-1 is associated with advanced prostate cancer, metastatic disease and epithelial Akt activation'. Together they form a unique fingerprint.

    Cite this