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Expression of claudin 18.2 in poorly cohesive carcinoma and its association with clinicopathologic parameters in East Asian patients

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dc.contributor.author박지현-
dc.date.accessioned2025-07-09T08:28:06Z-
dc.date.available2025-07-09T08:28:06Z-
dc.date.issued2024-11-
dc.identifier.issn0344-0338-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/206371-
dc.description.abstractBackground: Poorly cohesive carcinoma (PCC) is a distinct subtype of gastric cancer with limited therapeutic options. This study investigated claudin (CLDN) 18.2 expression status in PCCs using a 43-13 A clone. Methods: We retrospectively collected 178 consecutive surgically resected stage Ⅱ-Ⅲ gastric cancer samples. Tissue microarray blocks were constructed for CLDN18.2 immunohistochemical staining. We studied CLDN18.2 expression and its association with clinicopathologic parameters. Results: CLDN18.2 positivity (defined by ≥ 75 % of tumor cells showing moderate to strong membranous positivity) was found in 34.8 % of the PCC cases (62/178). Approximately half of the CLDN18.2 positive PCCs demonstrated heterogeneous expression (51.6 %, 32/62). CLDN18.2 positivity was not associated with any clinicopathologic parameters examined. However, CLDN18.2 positivity tended to be more frequent in E-cadherin-positive PCCs (no loss of expression) than in E-cadherin-negative PCCs (loss of expression) (50 % vs. 27.7 %). The CLDN18.2 expression level, represented by the H-score, gradually decreased as the paraffin block storage time increased (P = 0.046). Overall survival and disease-free survival analyses showed no significant difference between CLDN18.2-positive and negative PCCs. Conclusions: A significant portion of surgically resected PCC specimens showed CLDN18.2 positivity. Additionally, since the expression level of CLDN18.2 gradually decreases with increased paraffin block storage time, reflex testing can be considered at the time of the cancer diagnosis.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish, German, French, English(Summary), German(Summary)-
dc.publisherGustav Fischer Verlag-
dc.relation.isPartOfPATHOLOGY RESEARCH AND PRACTICE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHBiomarkers, Tumor* / analysis-
dc.subject.MESHBiomarkers, Tumor* / metabolism-
dc.subject.MESHCarcinoma / metabolism-
dc.subject.MESHCarcinoma / mortality-
dc.subject.MESHCarcinoma / pathology-
dc.subject.MESHClaudins* / metabolism-
dc.subject.MESHEast Asian People-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPrognosis-
dc.subject.MESHRetrospective Studies-
dc.subject.MESHStomach Neoplasms* / metabolism-
dc.subject.MESHStomach Neoplasms* / pathology-
dc.titleExpression of claudin 18.2 in poorly cohesive carcinoma and its association with clinicopathologic parameters in East Asian patients-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Pathology (병리학교실)-
dc.contributor.googleauthorMoonsik Kim-
dc.contributor.googleauthorByung Woog Kang-
dc.contributor.googleauthorJihyun Park-
dc.contributor.googleauthorJin Ho Baek-
dc.contributor.googleauthorJong Gwang Kim-
dc.identifier.doi10.1016/j.prp.2024.155628-
dc.contributor.localIdA06741-
dc.relation.journalcodeJ02474-
dc.identifier.eissn1618-0631-
dc.identifier.pmid39368365-
dc.subject.keyword43–14A-
dc.subject.keywordCLDN18.2-
dc.subject.keywordImmunohistochemistry-
dc.subject.keywordPoorly cohesive carcinoma-
dc.subject.keywordZolbetuximab-
dc.contributor.alternativeNamePark, Jihyun-
dc.contributor.affiliatedAuthor박지현-
dc.citation.volume263-
dc.citation.startPage155628-
dc.identifier.bibliographicCitationPATHOLOGY RESEARCH AND PRACTICE, Vol.263 : 155628, 2024-11-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers

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