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Evaluation of MUC1, MUC2, MUC5AC, and MUC6 expression differences in lung adenocarcinoma subtypes by using a final immunoreactivity score (FIRS)

dc.contributor.coauthorYilmazbayhan, Dilek
dc.contributor.coauthorVuralli Bakkaloglu, Dogu
dc.contributor.coauthorOzluk, Yasemi
dc.contributor.coauthorBuyuk, Melek
dc.contributor.coauthorOzkan, Berker
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorFırat, Pınar Arıkan
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T23:49:12Z
dc.date.issued2023
dc.description.abstractObjective: Lung adenocarcinomas are divided into acinar, lepidic, papillary, micropapillary, and solid predominant subtypes according to the current World Health Organization (WHO) classification. We designed this retrospective study to demonstrate profiles of MUC expression (MUC1, MUC2, MUC5AC, and MUC6) of different histologic patterns within the same tumor among pulmonary adenocarcinomas and investigate correlations of MUC expression with clinicopathologic features. Material and Method: We analyzed the expression of mucins (MUC1, MUC2, MUC5AC, and MUC6) in a series of 99 resected lung adenocarcinomas, which included a total of 193 patterns (71 acinar, 30 lepidic, 25 papillary, 20 micropapillary, 34 solid and 13 mucinous) and calculated a final immune reactivity score (FIRS) per tumor. Results: MUC1 IRS scores were significantly higher in lepidic and solid patterns compared with mucinous patterns (p=0.013). MUC2 expression was seen only in three cases (1 acinar, 2 mucinous). MUC5AC and MUC2 expression was more common in mucinous patterns (p<0.001 and p=0.028, respectively). MUC6 expression was only detected in seven patterns and the expression was weak. No significant difference was seen among histologic patterns for the staining scores of MUC6. Mucinous adenocarcinoma differed from other histologic subtypes regarding MUC1 and MUC5AC expression. Mucinous adenocarcinoma showed less MUC1 expression with lower IRS scores and higher MUC5AC expression. Tumor size (p=0.006), lymphatic invasion (p=0.018), vascular invasion (p=0.025), perineural invasion (p=0.019), MUC1 IRS scores (p=0.018), and MUC1 IRS scores >8.5 (p=0.018) were significant predictors for lymph node metastasis. Conclusion: An alternative scoring for MUC1 can be used as a predictor for lymph node metastasis regardless of the histologic subtype. ©️ 2022 The Author(s).
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.indexedbyTR Dizin
dc.description.indexedbyWOS
dc.description.issue1
dc.description.openaccessYES
dc.description.publisherscopeNational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipFunding received from the Scientific Research Projects Unit of Istanbul University for this study.
dc.description.volume39
dc.identifier.doi10.5146/tjpath.2022.01593
dc.identifier.issn1018-5615
dc.identifier.scopus2-s2.0-85146365205
dc.identifier.urihttps://doi.org/10.5146/tjpath.2022.01593
dc.identifier.urihttps://hdl.handle.net/20.500.14288/14333
dc.identifier.wos961956500008
dc.keywordsImmune reactivity score
dc.keywordsImmunohistochemistry
dc.keywordsLung adenocarcinoma
dc.keywordsMUC1
dc.keywordsMucin expression adenocarcinoma of lung
dc.keywordsAdenocarcinoma
dc.keywordsMucinous
dc.keywordsBiomarkers
dc.keywordsTumor
dc.keywordsHumans
dc.keywordsLung neoplasms
dc.keywordsLymphatic metastasis
dc.keywordsMucin 5AC
dc.keywordsMucin-1
dc.keywordsMucin-2
dc.keywordsMucin-6
dc.keywordsRetrospective studies
dc.keywordsMUC2 protein
dc.keywordsMUC5AC protein
dc.keywordsMUC6 protein
dc.keywordsHuman
dc.keywordsMucin 1
dc.keywordsMucin 2
dc.keywordsMucin 5AC
dc.keywordsMucin 6
dc.language.isoeng
dc.publisherFederation of Turkish Pathology Societies
dc.relation.ispartofTurk Patoloji Dergisi
dc.subjectPathology
dc.titleEvaluation of MUC1, MUC2, MUC5AC, and MUC6 expression differences in lung adenocarcinoma subtypes by using a final immunoreactivity score (FIRS)
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorFırat, Pınar Arıkan
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

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