The RNA‐Binding Protein Musashi‐1 Regulates Proteasome Subunit Expression in Breast Cancer‐ and Glioma‐Initiating Cells. (3rd January 2014)

• Record Type: Journal Article
• Authors: Lagadec, Chann; Vlashi, Erina; Frohnen, Patricia; Alhiyari, Yazeed; Chan, Mabel; Pajonk, Frank
• Is Part Of: Stem cells. Volume 32:Number 1(2014:Jan.)
• Page Start: 135
• Page End: 144
• Publication Date: 2014-01-03
• Subjects: Breast cancer stem cells -- Glioma stem cells -- Notch -- Proteasome -- Musashi -- NF‐Y; Cloning -- Periodicals; Clone cells -- Periodicals; Stem cells -- Periodicals; Cell Differentiation -- Periodicals; Cell Division -- Periodicals; Clone Cells -- Periodicals; Hematopoietic Stem Cells -- Periodicals; Stem Cells -- Periodicals; 571.84
• DOI: 10.1002/stem.1537
• Languages: English
• ISSNs: 1066-5099

Abstract

Abstract: Cancer stem cells (CSCs) or tumor‐initiating cells, similar to normal tissue stem cells, rely on developmental pathways, such as the Notch pathway, to maintain their stem cell state. One of the regulators of the Notch pathway is Musashi‐1, a mRNA‐binding protein. Musashi‐1 promotes Notch signaling by binding to the mRNA of Numb, the negative regulator of Notch signaling, thus preventing its translation. CSCs have also been shown to downregulate their 26S proteasome activity in several types of solid tumors, thus making them resistant to proteasome‐inhibitors used as anticancer agents in the clinic. Interestingly, the Notch pathway can be inhibited by proteasomal degradation of the Notch intracellular domain (Notch‐ICD); therefore, downregulation of the 26S proteasome activity can lead to stabilization of Notch‐ICD. Here, we present evidence that the downregulation of the 26S proteasome in CSCs constitutes another level of control by which Musashi‐1 promotes signaling through the Notch pathway and maintenance of the stem cell phenotype of this subpopulation of cancer cells. We demonstrate that Musashi‐1 mediates the downregulation of the 26S proteasome by binding to the mRNA of NF‐YA, the transcriptional factor regulating 26S proteasome subunit expression, thus providing an additional route by which the degradation of Notch‐ICD is prevented, and Notch signaling is sustained. Stem Cells 2014;32:135–144