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Using public data of normal human tissues, we found that <jats:styled-content style=\"fixed-case\">mRNA<\/jats:styled-content> and protein levels of mucin 5B (<jats:styled-content style=\"fixed-case\">MUC<\/jats:styled-content>5B) and carbonic anhydrase 9 (<jats:styled-content style=\"fixed-case\">CA<\/jats:styled-content>9) were highly increased in gallbladder tissues. In addition, previous evidence has shown that claudin 18 (<jats:styled-content style=\"fixed-case\">CLDN<\/jats:styled-content>18) protein expression is higher in <jats:styled-content style=\"fixed-case\">GBC<\/jats:styled-content>. The aim of this study was to perform an analysis of these cell surface proteins during the histological progression of <jats:styled-content style=\"fixed-case\">GBC<\/jats:styled-content> in order to identify their theranostic potential.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods and results<\/jats:title><jats:p><jats:styled-content style=\"fixed-case\">MUC<\/jats:styled-content>5B expression, <jats:styled-content style=\"fixed-case\">CA<\/jats:styled-content>9 expression and <jats:styled-content style=\"fixed-case\">CLDN<\/jats:styled-content>18 expression were examined by immunohistochemistry in a series of 179 chronic cholecystitis (including 16 metaplastic tissues), 15 dysplasia and 217 <jats:styled-content style=\"fixed-case\">GBC<\/jats:styled-content> samples by the use of tissue microarray analysis. A composite staining score was calculated from staining intensity and percentage of positive cells. Immunohistochemical analysis showed high expression of <jats:styled-content style=\"fixed-case\">MUC<\/jats:styled-content>5B and <jats:styled-content style=\"fixed-case\">CA<\/jats:styled-content>9 among normal epithelium, metaplastic tissues, and dysplastic tissues. However, expression of both proteins was observed in roughly 50% of <jats:styled-content style=\"fixed-case\">GBC<\/jats:styled-content> samples. In contrast, <jats:styled-content style=\"fixed-case\">CLDN<\/jats:styled-content>18 was absent in normal epithelium, but its expression was higher in metaplastic cells. Among <jats:styled-content style=\"fixed-case\">GBC<\/jats:styled-content> cases, approximately half showed high <jats:styled-content style=\"fixed-case\">CLDN<\/jats:styled-content>18 expression. No associations were found between <jats:styled-content style=\"fixed-case\">MUC<\/jats:styled-content>5B, <jats:styled-content style=\"fixed-case\">CA<\/jats:styled-content>9 and <jats:styled-content style=\"fixed-case\">CLDN<\/jats:styled-content>18 expression and any clinicopathological features.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p><jats:styled-content style=\"fixed-case\">CLDN<\/jats:styled-content>18 is a new metaplasia marker in gallbladder tissues, and is conserved in approximately half of <jats:styled-content style=\"fixed-case\">GBC<\/jats:styled-content> cases. <jats:styled-content style=\"fixed-case\">MUC<\/jats:styled-content>5B and <jats:styled-content style=\"fixed-case\">CA<\/jats:styled-content>9 are highly conserved during <jats:styled-content style=\"fixed-case\">GBC<\/jats:styled-content> histological progression. The three markers are potential theranostic markers, in particular <jats:styled-content style=\"fixed-case\">CA<\/jats:styled-content>9 and <jats:styled-content style=\"fixed-case\">CLDN<\/jats:styled-content>18, for which there are already targeted therapies available.<\/jats:p><\/jats:sec>","DOI":"10.1111\/his.13797","type":"journal-article","created":{"date-parts":[[2018,12,19]],"date-time":"2018-12-19T14:29:08Z","timestamp":1545229748000},"page":"597-607","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":21,"title":["Mucin 5B, carbonic anhydrase 9 and claudin 18 are potential theranostic markers of gallbladder carcinoma"],"prefix":"10.1111","volume":"74","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-0731-2715","authenticated-orcid":false,"given":"Jaime A","family":"Espinoza","sequence":"first","affiliation":[{"name":"SciLifeLab Division of Genome Biology Department of Medical Biochemistry and Biophysics Karolinska Institutet, Solna Stockholm Sweden"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ismael","family":"Riquelme","sequence":"additional","affiliation":[{"name":"Instituto de Ciencias Biom\u00e9dicas Facultad de Ciencias de la Salud Universidad Aut\u00f3noma de Chile Temuco Chile"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Eduardo A","family":"Sagredo","sequence":"additional","affiliation":[{"name":"Centro de Investigaci\u00f3n y Tratamiento del C\u00e1ncer Facultad de Medicina Universidad de Chile Santiago Chile"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lorena","family":"Rosa","sequence":"additional","affiliation":[{"name":"Department of Pathology School of Medicine Pontificia Universidad Cat\u00f3lica de Chile Santiago Chile"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Patricia","family":"Garc\u00eda","sequence":"additional","affiliation":[{"name":"Department of Pathology School of Medicine Pontificia 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