The Polycomb Group Protein Bmi-1 Is Essential for the Growth of Multiple Myeloma Cells

Bmi-1 is a member of the Polycomb group family of proteins that function in the epigenetic silencing of genes governing self-renewal, differentiation, and proliferation. Bmi-1 was first identified through its ability to accelerate c-Myc-induced lymphomagenesis. Subsequent studies have further suppor...

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Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 2010-07, Vol.70 (13), p.5528-5538
Hauptverfasser: JAGANI, Zainab, WIEDERSCHAIN, Dmitri, WARMUTH, Markus, SELLERS, William R, DORSCH, Marion, LOO, Alice, DAN HE, MOSHER, Rebecca, FORDJOUR, Paul, MONAHAN, John, MORRISSEY, Michael, YAO, Yung-Mae, LENGAUER, Christoph
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Sprache:eng
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Zusammenfassung:Bmi-1 is a member of the Polycomb group family of proteins that function in the epigenetic silencing of genes governing self-renewal, differentiation, and proliferation. Bmi-1 was first identified through its ability to accelerate c-Myc-induced lymphomagenesis. Subsequent studies have further supported an oncogenic role for Bmi-1 in several cancers including those of the breast, lung, prostate, and brain. Using a stable and inducible shRNA system to silence Bmi-1 gene expression, we show a novel role for Bmi-1 in regulating the growth and clonogenic capacity of multiple myeloma cells both in vitro and in vivo. Moreover, to elucidate novel gene targets controlled by Bmi-1, global transcriptional profiling studies were performed in the setting of induced loss of Bmi-1 function. We found that the expression of the proapoptotic gene Bim is negatively regulated by Bmi-1 and that Bim knockdown functionally rescues the apoptotic phenotype induced upon loss of Bmi-1. Therefore, these studies not only highlight Bmi-1 as a cancer-dependent factor in multiple myeloma, but also elucidate a novel antiapoptotic mechanism for Bmi-1 function involving the suppression of Bim.
ISSN:0008-5472
1538-7445
DOI:10.1158/0008-5472.can-09-4229