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BCL-3 promotes a cancer stem cell phenotype by enhancing β-catenin signalling in colorectal tumour cells

Research output: Contribution to journalArticle

Original languageEnglish
Article numberdmm037697
Number of pages12
JournalDisease Models and Mechanisms
Volume12
Issue number3
Early online date4 Mar 2019
DOIs
DateAccepted/In press - 15 Feb 2019
DateE-pub ahead of print - 4 Mar 2019
DatePublished (current) - 4 Mar 2019

Abstract

To decrease bowel cancer incidence and improve survival, we need to understand the mechanisms that drive tumorigenesis. Recently BCL-3 (a key regulator of NF-κB signalling) has been recognised as an important oncogenic player in solid tumours. Although reported to be over-expressed in a subset of colorectal cancers (CRC), the role of BCL-3 expression in colorectal tumorigenesis remains poorly understood. Despite evidence in the literature that BCL-3 may interact with β-catenin it is perhaps surprising, given the importance of deregulated Wnt/β-catenin signalling in colorectal carcinogenesis, that the functional significance of this interactions is not known. Here we show for the first time that BCL-3 acts as a co-activator of β-catenin/TCF-mediated transcriptional activity in colorectal cancer cells and that this interaction is important for Wnt-regulated intestinal stem cell gene expression. We demonstrate that targeting BCL-3 expression (using RNA interference) reduced βcatenin/TCF-dependent transcription and the expression of intestinal stem cell genes LGR5 and ASCL2. In contrast, the expression of canonical Wnt-targets C-Myc and Cyclin D1 remained unchanged. Furthermore, we show that BCL-3 increases the functional stem cell phenotype as shown by colorectal spheroid and tumoursphere formation in 3D culture conditions. We propose that BCL-3 acts as a driver of the stem-cell phenotype in CRC cells potentially promoting tumour cell plasticity and therapeutic resistance. As recent reports highlight the limitations of directly targeting cancer stem cells (CSC), we believe that identifying and targeting drivers of stem cell plasticity have significant potential as new therapeutic targets

    Research areas

  • BCL3, Spheroid, Wnt, ASCL2, LGR5, NF-kB, NF-kappa B

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    Rights statement: This is the final published version of the article (version of record). It first appeared online via The Company of Biologists Ltd at https://www.doi.org/10.1242/dmm.037697 . Please refer to any applicable terms of use of the publisher.

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    Licence: CC BY

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