Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/28272
Title: BMP antagonist CHRDL2 enhances the cancer stem cell phenotype and increases chemotherapy resistance in Colorectal Cancer
Authors: Clarkson, E
Lewis, A
Keywords: colorectal cancer;chordin-like 2;bone-morphogenic protein;WNT signalling pathway;cancer stem cell
Issue Date: 26-Jan-2024
Publisher: Cold Spring Harbor Laboratory (bioRxiv) [submitted to Gut (BMJ)]
Citation: Clarkson, E. and Lewis, A. (2024) 'BMP antagonist CHRDL2 enhances the cancer stem cell phenotype and increases chemotherapy resistance in Colorectal Cancer', Gut, 0 (submitted), pp. 1 - [38].
Abstract: Chordin-like-2 (CHRDL2) is a secreted BMP antagonist, with overexpression and genomic variants associated with colorectal cancer (CRC) risk. BMP signalling in the normal intestinal epithelium operates in opposition to the WNT signalling pathway, which maintains stem-cells and self-renewal. Elevated WNT signalling leads to expansion of the stem cell compartment and hyperproliferation, defining characteristics of CRC. Here, we explored the impact of CHRDL2 overexpression on CRC cells and normal intestinal organoids to investigate whether CHRDL2’s inhibition of BMP signalling intensified WNT signalling, and enhanced the cancer stem-cell phenotype. CHRDL2 increased cell survival during chemotherapy and irradiation with associated activation of DNA damage response pathways. Organoids treated with secreted CHRDL2 exhibited elevated levels of stem cell markers and reduced differentiation. RNA-seq analysis revealed that CHRDL2 increased the expression of stem cell markers and well-established cancer-associated pathways. We suggest that CHRDL2 overexpression can augment the stem-cell potential of CRC and normal intestinal cells.
Description: Data visualisation and R: Data was cleaned and significant data was extracted using R software. Graphs we generated using R studio 4.1.0 using libraries ggplot2 and heatmap2. Gene-set-enrichment analysis was performed using the GSEA software 4.2.3. The Chip annotation platform used was Human_Ensembl_Transcript_ID_MSigDB.v7.5.1.chip. Gene sets used: * c6.all.v7.5.1.symbols.gmt * h.all.v7.5.1.symbols.gmt * GOBP_REGULATION_OF_BMP_SIGNALING_PATHWAY * enplot_REACTOME_PI3K_AKT_SIGNALING_IN_CANCER_13 * enplot_GOMF_BMP_RECEPTOR_BINDING_58 * WP_NRF2_PATHWAY.v2023.1.Hs.
The article currently archived on this institutional repository is a BioRxiv preprint available online at https://doi.org/10.1101/2024.01.23.576664 . It has not been certified by peer review (see: https://www.biorxiv.org/about/FAQ#unrefereed). It has been submitted to Gut pending peer review and acceptance for publication.
URI: https://bura.brunel.ac.uk/handle/2438/28272
DOI: https://doi.org/10.1101/2024.01.23.576664
ISSN: 0017-5749
Other Identifiers: ORCID iD: Eloise Clarkson https://orcid.org/0009-0004-4740-0498
ORCID iD: Annabelle Lewis https://orcid.org/0000-0003-1876-1927
Appears in Collections:Dept of Life Sciences Research Papers

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