Publication:
Stromal heterogeneity in pancreatic cancer and chronic pancreatitis

dc.contributor.coauthorHaeberle, Lena
dc.contributor.coauthorSteiger, Katja
dc.contributor.coauthorSchlitter, Anna Melissa
dc.contributor.coauthorSafi, Sami Alexander
dc.contributor.coauthorKnoefel, Wolfram Trudo
dc.contributor.coauthorEsposito, Irene
dc.contributor.departmentN/A
dc.contributor.kuauthorErkan, Murat Mert
dc.contributor.kuprofileFaculty Member
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.unitKoç University Hospital
dc.contributor.yokid214689
dc.date.accessioned2024-11-09T23:39:08Z
dc.date.issued2018
dc.description.abstractBackground/objectives: An abundant stromal reaction is a hallmark of pancreatic ductal adenocarcinoma (PDAC) and chronic pancreatitis (CP). The cells mainly responsible for the stromal reaction are activated pancreatic stellate cells (PSCs). Despite their crucial role, PSCs are not well characterized. PSCs share characteristics with the better-known hepatic stellate cells (HSCs). The aim of this study was a detailed analysis of PSCs in PDAC and CP. Methods: Whole-slide specimens of CP (n = 12) and PDAC (n = 10) were studied by histochemistry and immunohistochemistry. The stroma was evaluated using Movat's pentachrome stain. PSCs were tested by immunohistochemistry for PSC markers (alpha-SMA, CD34, desmin, NGFR, SPARC and tenascin C) and HSC markers (alpha-crystallin B, CD56, NGF, NT-3, synaptophysin and TrkC). Alpha-SMA, tenascin C, SPARC and NT-3 staining were verified on tissue micro arrays (TMAs) from a well-characterized cohort of 223 PDAC patients. PSCs isolated from human PDAC and CP tissue samples as well as HSCs were evaluated by immunofluorescence. Results: While the stroma of CP cases was characterized by a collagen-rich fibrosis, PDAC stroma displayed higher mucin content (p = 0.0002). PSCs showed variable expression of tested markers. In PDAC samples, staining of most markers was found around tumor complexes, while CP samples showed a greater variety of localizations. Alpha-SMA staining correlated with collagen-rich fibrosis (p = 0.012), while NT-3 staining correlated with mucin-rich stroma (p = 0.008). A peritumoral staining was confirmed for alpha-SMA, tenascin C, SPARC and NT-3 in the PDAC TMA cohort (n = 223). In a subgroup of patients with pancreatic head tumors and UICC 2009 IIB (n = 144), alpha-SMA staining intensity was a prognostic factor for overall survival at uni- and multivariate analysis (p = 0.036 and p = 0.002). Conclusions: The close similarities between PSCs and HSCs were confirmed. Heterogeneous expression patterns of the tested markers might reflect different levels of activation or differentiation, or even multiple subpopulations of PSCs. Survival analysis suggests an impact of stromal composition on survival. (C) 2018 IAP and EPC. Published by Elsevier B.V. All rights reserved.
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue5
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.volume18
dc.identifier.doi10.1016/j.pan.2018.05.004
dc.identifier.eissn1424-3911
dc.identifier.issn1424-3903
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85047064338
dc.identifier.urihttp://dx.doi.org/10.1016/j.pan.2018.05.004
dc.identifier.urihttps://hdl.handle.net/20.500.14288/13066
dc.identifier.wos437632900012
dc.keywordsChronic pancreatitis
dc.keywordsPancreatic cancer
dc.keywordsPancreatic stellate cells
dc.keywordsStromal reaction
dc.keywordsTumor microenvironment stellate cells
dc.keywordsDuctal adenocarcinoma
dc.keywordsPerineural invasion
dc.keywordsTrk receptors
dc.keywordsExpression
dc.keywordsFibrosis
dc.keywordsIdentification
dc.keywordsSubtypes
dc.keywordsTumor
dc.keywordsCarcinoma
dc.languageEnglish
dc.publisherElsevier Science Bv
dc.sourcePancreatology
dc.subjectGastroenterology
dc.subjectHepatology
dc.titleStromal heterogeneity in pancreatic cancer and chronic pancreatitis
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.authorid0000-0002-2753-0234
local.contributor.kuauthorErkan, Murat Mert

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