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                  <mods:namePart>Sancho, Patricia</mods:namePart>
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                  <mods:namePart>Hermann, Patrick C</mods:namePart>
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                  <mods:namePart>Heeschen, Christopher</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2026-02-20T21:43:00Z</mods:dateAccessioned>
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                  <mods:dateIssued encoding="iso8601">2015-12</mods:dateIssued>
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               <mods:identifier type="citation">Gut  . 2015 Dec;64(12):1921-35.</mods:identifier>
               <mods:identifier type="journal">GUT</mods:identifier>
               <mods:identifier type="pubmedID">25841238</mods:identifier>
               <mods:identifier type="uri">https://hdl.handle.net/20.500.12105/27250</mods:identifier>
               <mods:abstract>The tumour stroma/microenvironment not only provides structural support for tumour development, but more importantly it provides cues to cancer stem cells (CSCs) that regulate their self-renewal and metastatic potential. This is certainly true for pancreatic ductal adenocarcinomas (PDAC), where tumour-associated fibroblasts, pancreatic stellate cells and immune cells create an abundant paracrine niche for CSCs via microenvironment-secreted factors. Thus understanding the role that tumour stroma cells play in PDAC development and CSC biology is of utmost importance.Microarray analyses, tumour microarray immunohistochemical assays, in vitro co-culture experiments, recombinant protein treatment approaches and in vivo intervention studies were performed to understand the role that the immunomodulatory cationic antimicrobial peptide 18/LL-37 (hCAP-18/LL-37) plays in PDAC biology.We found that hCAP-18/LL-37 was strongly expressed in the stroma of advanced primary and secondary PDAC tumours and is secreted by immune cells of the stroma (eg, tumour-associated macrophages) in response to tumour growth factor-β1 and particularly CSC-secreted Nodal/ActivinA. Treatment of pancreatic CSCs with recombinant LL-37 increased pluripotency-associated gene expression, self-renewal, invasion and tumourigenicity via formyl peptide receptor 2 (FPR2)- and P2X purinoceptor 7 receptor (P2X7R)-dependent mechanisms, which could be reversed by inhibiting these receptors. Importantly, in a genetically engineered mouse model of K-Ras-driven pancreatic tumourigenesis, we also showed that tumour formation was inhibited by either reconstituting these mice with bone marrow from cathelicidin-related antimicrobial peptide (ie, murine homologue of hCAP-18/LL-37) knockout mice or by pharmacologically inhibiting FPR2 and P2X7R.Thus, hCAP-18/LL-37 represents a previously unrecognised PDAC microenvironment factor that plays a critical role in pancreatic CSC-mediated tumourigenesis.</mods:abstract>
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               <mods:subject>
                  <mods:topic>ANTIBACTERIAL PEPTIDE</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>MACROPHAGES</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>PANCREATIC CANCER</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>STEM CELLS</mods:topic>
               </mods:subject>
               <mods:titleInfo>
                  <mods:title>Microenvironmental hCAP-18/LL-37 promotes pancreatic ductal adenocarcinoma by activating its cancer stem cell compartment.</mods:title>
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