Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/28272
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dc.contributor.authorClarkson, E-
dc.contributor.authorLewis, A-
dc.date.accessioned2024-02-09T17:40:04Z-
dc.date.available2024-02-09T17:40:04Z-
dc.date.issued2024-01-26-
dc.identifierORCID iD: Eloise Clarkson https://orcid.org/0009-0004-4740-0498-
dc.identifierORCID iD: Annabelle Lewis https://orcid.org/0000-0003-1876-1927-
dc.identifier.citationClarkson, 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].en_US
dc.identifier.issn0017-5749-
dc.identifier.urihttps://bura.brunel.ac.uk/handle/2438/28272-
dc.descriptionData 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.en_US
dc.descriptionThe 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 It has not been certified by peer review (see: https://www.biorxiv.org/about/FAQ#unrefereed).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.-
dc.description.abstractChordin-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.en_US
dc.description.sponsorshipBowel Research UK: project title “Investigating variations in two genes that increase the risk of bowel cancer”. ... [submitted article - modify metadata to match when published and split off bioRxiv DOI on CRIS! DB 2024-02-09]en_US
dc.format.mediumPrint-Electronic-
dc.language.isoen_USen_US
dc.publisherCold Spring Harbor Laboratory (bioRxiv) [submitted to Gut (BMJ)]en_US
dc.relation.urihttps://www.biorxiv.org/content/10.1101/2024.01.23.576664v1-
dc.rightsThe copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license (https://creativecommons.org/licenses/by/4.0/).-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subjectcolorectal cancer-
dc.subjectchordin-like 2-
dc.subjectbone-morphogenic protein-
dc.subjectWNT signalling pathway-
dc.subjectcancer stem cell-
dc.titleBMP antagonist CHRDL2 enhances the cancer stem cell phenotype and increases chemotherapy resistance in Colorectal Canceren_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.1101/2024.01.23.576664-
dc.relation.isPartOfBioRxiv-
pubs.publication-statusSubmitted-
dc.identifier.eissn1468-3288-
dc.rights.holderauthor/funder-
Appears in Collections:Dept of Life Sciences Research Papers

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