Membranous and nuclear staining of CLDN18 in HPV‐independent and HPV‐associated endocervical adenocarcinomas

Abstract Objectives A classification system for endocervical adenocarcinoma (ECA) based on high‐risk human papillomavirus (HPV) status has been established; however, the immunohistochemical markers distinguishing HPV‐independent and HPV‐associated ECAs have not been fully described. Here, we aimed t...

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Published in:Cancer Medicine
Main Authors: Xiuzhen Du, Yanjiao Hu, Xiaoyu Ji, Lei Sui, Qingmei Zheng, Kejuan Song, Teng Lv, Yulong Chen, Han Zhao, Shuzhen Dai, Peng Zhao, Qin Yao
Format: Article
Language:English
Published: Wiley 2023-01-01
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Online Access:https://doi.org/10.1002/cam4.5029
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author Xiuzhen Du
Yanjiao Hu
Xiaoyu Ji
Lei Sui
Qingmei Zheng
Kejuan Song
Teng Lv
Yulong Chen
Han Zhao
Shuzhen Dai
Peng Zhao
Qin Yao
author_facet Xiuzhen Du
Yanjiao Hu
Xiaoyu Ji
Lei Sui
Qingmei Zheng
Kejuan Song
Teng Lv
Yulong Chen
Han Zhao
Shuzhen Dai
Peng Zhao
Qin Yao
author_sort Xiuzhen Du
collection DOAJ
container_title Cancer Medicine
description Abstract Objectives A classification system for endocervical adenocarcinoma (ECA) based on high‐risk human papillomavirus (HPV) status has been established; however, the immunohistochemical markers distinguishing HPV‐independent and HPV‐associated ECAs have not been fully described. Here, we aimed to characterize ECA immunopathological features. Methods We evaluated the immunohistochemical profile of CLDN18, CDX2, PAX8, p16, p53, and CEA in 60 ECAs comprising 10 HPV‐independent ECAs and 50 HPV‐associated ECAs. Both the membranous and nuclear expression levels of CLDN18 were analyzed. Results Membranous CLDN18 (CLDN18 [M]) was found to be expressed in the mucinous epithelium of all HPV‐independent ECAs, including eight gastric‐type ECAs (G‐ECAs), one endometrioid ECA, and one clear cell ECA, but no nuclear CLDN18 (CLDN18 [N]) expression was detected in HPV‐independent ECAs. Among HPV‐associated ECAs, CLDN18 (M) expression levels in intestinal‐type (I‐ECAs) and usual‐type ECAs (U‐ECAs) were significantly different from those in invasive stratified mucin‐producing (iSMILE) carcinomas (p = 0.036). Positive CLDN18 (M) staining was present in 55.6% (5/9) of intestinal‐type and 39.4% (13/33) of usual‐type ECAs and was not present in iSMILE ECAs. Silva pattern C cancers expressed higher levels of CLDN18 (M) than Silva pattern A and B cancers (p = 0.004), whereas the CLDN18 (N) expression levels in cancers showing Silva pattern A were significantly higher than those in cancers exhibiting Silva patterns B and C (p < 0.001). Conclusion Membranous CLDN18 is expressed in ECAs and is particularly frequently expressed in HPV‐independent ECAs, and membranous CLDN18 expression has potential as a therapeutic target. Nuclear staining of CLDN18 is a new immunohistochemical marker for diagnosing Silva pattern A HPV‐associated ECAs and is associated with a good prognosis. Further studies should investigate the therapeutic and prognostic significance of membranous and nuclear CLDN18 expression and develop a related test that can be implemented in the clinical evaluation of ECAs.
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spelling doaj-art-133579de95724aecb60e58664f4da1702025-08-19T19:25:52ZengWileyCancer Medicine2045-76342023-01-011221441145010.1002/cam4.5029Membranous and nuclear staining of CLDN18 in HPV‐independent and HPV‐associated endocervical adenocarcinomasXiuzhen Du0Yanjiao Hu1Xiaoyu Ji2Lei Sui3Qingmei Zheng4Kejuan Song5Teng Lv6Yulong Chen7Han Zhao8Shuzhen Dai9Peng Zhao10Qin Yao11Department of Obstetrics and Gynecology The Affiliated Hospital of Qingdao University Qingdao Shandong ChinaDepartment of Pathology The affiliated Hospital of Qingdao University Qingdao Shandong ChinaDepartment of Obstetrics and Gynecology The Affiliated Hospital of Qingdao University Qingdao Shandong ChinaDepartment of Obstetrics and Gynecology The Affiliated Hospital of Qingdao University Qingdao Shandong ChinaDepartment of Obstetrics and Gynecology The Affiliated Hospital of Qingdao University Qingdao Shandong ChinaDepartment of Obstetrics and Gynecology The Affiliated Hospital of Qingdao University Qingdao Shandong ChinaDepartment of Obstetrics and Gynecology The Affiliated Hospital of Qingdao University Qingdao Shandong ChinaDepartment of Obstetrics and Gynecology The Affiliated Hospital of Qingdao University Qingdao Shandong ChinaDepartment of Pathology The affiliated Hospital of Qingdao University Qingdao Shandong ChinaDepartment of Obstetrics and Gynecology The Affiliated Hospital of Qingdao University Qingdao Shandong ChinaDepartment of Pathology The affiliated Hospital of Qingdao University Qingdao Shandong ChinaDepartment of Obstetrics and Gynecology The Affiliated Hospital of Qingdao University Qingdao Shandong ChinaAbstract Objectives A classification system for endocervical adenocarcinoma (ECA) based on high‐risk human papillomavirus (HPV) status has been established; however, the immunohistochemical markers distinguishing HPV‐independent and HPV‐associated ECAs have not been fully described. Here, we aimed to characterize ECA immunopathological features. Methods We evaluated the immunohistochemical profile of CLDN18, CDX2, PAX8, p16, p53, and CEA in 60 ECAs comprising 10 HPV‐independent ECAs and 50 HPV‐associated ECAs. Both the membranous and nuclear expression levels of CLDN18 were analyzed. Results Membranous CLDN18 (CLDN18 [M]) was found to be expressed in the mucinous epithelium of all HPV‐independent ECAs, including eight gastric‐type ECAs (G‐ECAs), one endometrioid ECA, and one clear cell ECA, but no nuclear CLDN18 (CLDN18 [N]) expression was detected in HPV‐independent ECAs. Among HPV‐associated ECAs, CLDN18 (M) expression levels in intestinal‐type (I‐ECAs) and usual‐type ECAs (U‐ECAs) were significantly different from those in invasive stratified mucin‐producing (iSMILE) carcinomas (p = 0.036). Positive CLDN18 (M) staining was present in 55.6% (5/9) of intestinal‐type and 39.4% (13/33) of usual‐type ECAs and was not present in iSMILE ECAs. Silva pattern C cancers expressed higher levels of CLDN18 (M) than Silva pattern A and B cancers (p = 0.004), whereas the CLDN18 (N) expression levels in cancers showing Silva pattern A were significantly higher than those in cancers exhibiting Silva patterns B and C (p < 0.001). Conclusion Membranous CLDN18 is expressed in ECAs and is particularly frequently expressed in HPV‐independent ECAs, and membranous CLDN18 expression has potential as a therapeutic target. Nuclear staining of CLDN18 is a new immunohistochemical marker for diagnosing Silva pattern A HPV‐associated ECAs and is associated with a good prognosis. Further studies should investigate the therapeutic and prognostic significance of membranous and nuclear CLDN18 expression and develop a related test that can be implemented in the clinical evaluation of ECAs.https://doi.org/10.1002/cam4.5029CLDN18endocervical adenocarcinomaHPVimmunohistochemistrymembranous expressionnuclear expression
spellingShingle Xiuzhen Du
Yanjiao Hu
Xiaoyu Ji
Lei Sui
Qingmei Zheng
Kejuan Song
Teng Lv
Yulong Chen
Han Zhao
Shuzhen Dai
Peng Zhao
Qin Yao
Membranous and nuclear staining of CLDN18 in HPV‐independent and HPV‐associated endocervical adenocarcinomas
CLDN18
endocervical adenocarcinoma
HPV
immunohistochemistry
membranous expression
nuclear expression
title Membranous and nuclear staining of CLDN18 in HPV‐independent and HPV‐associated endocervical adenocarcinomas
title_full Membranous and nuclear staining of CLDN18 in HPV‐independent and HPV‐associated endocervical adenocarcinomas
title_fullStr Membranous and nuclear staining of CLDN18 in HPV‐independent and HPV‐associated endocervical adenocarcinomas
title_full_unstemmed Membranous and nuclear staining of CLDN18 in HPV‐independent and HPV‐associated endocervical adenocarcinomas
title_short Membranous and nuclear staining of CLDN18 in HPV‐independent and HPV‐associated endocervical adenocarcinomas
title_sort membranous and nuclear staining of cldn18 in hpv independent and hpv associated endocervical adenocarcinomas
topic CLDN18
endocervical adenocarcinoma
HPV
immunohistochemistry
membranous expression
nuclear expression
url https://doi.org/10.1002/cam4.5029
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