Literature DB >> 33721119

CD146 immunohistochemical staining for the separation of benign from malignant mesothelial proliferations.

Taylor Salisbury1,2, Andrew Churg3,4.   

Abstract

The separation of benign from malignant mesothelial cells is often a challenging problem. Some studies have suggested that immunohistochemical staining of CD146 can be used to make this distinction, but there are marked differences in the reported results. Here, we assessed CD146 expression in tissue microarray specimens of 32 epithelioid reactive mesothelial hyperplasias, 17 spindle cell reactive mesothelial proliferations, 43 epithelioid mesotheliomas, and 31 sarcomatoid mesotheliomas. We found that, although the specificity of CD146 for epithelioid mesotheliomas versus reactive epithelial mesothelial proliferations was high (94%), staining intensity and extent was usually low and sensitivity was poor (23%). For sarcomatoid mesotheliomas versus reactive spindle cell mesothelial processes, both measures (33% sensitivity, 76% specificity) were inadequate. Furthermore, strong staining of endothelial cells and fibroblasts often created difficulties in interpretation. In comparison, BAP1 was lost in 21/43 (49%) epithelioid and 9/31 (29%) sarcomatoid mesotheliomas and methylthioadenosine phosphorylase (MTAP) was lost in 9/40 (23%) epithelioid and 7/29 (24%) sarcomatoid mesotheliomas from these TMAs. There was no association between CD146 staining and BAP1 or MTAP retention/loss. We conclude that CD146 staining is probably not useful for separating malignant from benign mesothelial proliferations.

Entities:  

Keywords:  Benign mesothelial reactions; CD146; Malignant mesothelioma

Year:  2021        PMID: 33721119     DOI: 10.1007/s00428-021-03077-7

Source DB:  PubMed          Journal:  Virchows Arch        ISSN: 0945-6317            Impact factor:   4.064


  1 in total

1.  Survivin expression as an independent predictor of overall survival in malignant peritoneal mesothelioma.

Authors:  Guozun Zhang; Dong-Liang Yang; Guoqi Zheng; Yufei Liang
Journal:  Oncol Lett       Date:  2020-04-02       Impact factor: 2.967

  1 in total

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