Differential expression of N-cadherin in pleural mesotheliomas and E- cadherin in lung adenocarcinomas in formalin-fixed, paraffin-embedded tissues

Aaron C. Han, Alejandro Peralta-Soler, Karen A. Knudsen, Margaret J. Wheelock, Keith R. Johnson, Hernando Salazar

Research output: Contribution to journalArticle

76 Citations (Scopus)

Abstract

The differential diagnosis of pleural mesotheliomas and lung adenocarcinomas presents a continued challenge in the practice of surgical pathology. Paraffin immunohistochemistry (IHC) using different panels of antibodies can be helpful in some cases, but, as yet, no antigen is expressed specifically in mesotheliomas nor in adenocarcinomas. Using well characterized monoclonal antibodies (MAb) that recognized distinct mesenchymal and epithelial adhesion proteins, N-cadherin (13A9 MAb) and E- cadherin (E9 MAb), respectively, we found previously that in frozen-section IHC mesotheliomas and adenocarcinomas had distinct cadherin phenotypes: mesotheliomas were positive for N-cadherin, and lung adenocarcinomas were positive for E-cadherin. Using antigen-retrieval methods, we successfully extended our study to formalin-fixed, paraffin-embedded tissue sections. Tumors from 28 patients (14 originally diagnosed as mesotheliomas, and 14 diagnosed as adenocarcinomas) were stained with 13A9 MAb and E9 MAb. Review of hematoxylin-eosin sections excluded from analysis one case previously diagnosed as mesothelioma, which represented a hemangiopericytoma. Of the remaining 27 cases, 12 of 13 mesotheliomas were positive for N-cadherin and negative for E-cadherin. The exception was a multifocal microscopic papillary tumor of apparent mesothelial origin, which was negative for both N-cadherin and E-cadherin. Conversely, 13 of 14 adenocarcinomas were E-cadherin positive and N-cadherin negative except for one adenocarcinoma with focal N-cadherin expression. One case of a poorly differentiated adenocarcinoma invading skeletal muscle was negative for both 13A9 and E9. These studies confirmed the utility of die cadherin antibodies in distinguishing pleural mesotheliomas from lung adenocarcinomas. The reactivity of the cadherin- specific antibodies with antigens in paraffin sections make them powerful and reliable markers in the practice of diagnostic surgical pathology.

Original languageEnglish (US)
Pages (from-to)641-645
Number of pages5
JournalHuman Pathology
Volume28
Issue number6
DOIs
StatePublished - Jan 1 1997

Fingerprint

Mesothelioma
Cadherins
Paraffin
Formaldehyde
Adenocarcinoma
Monoclonal Antibodies
Surgical Pathology
Adenocarcinoma of lung
Antigens
Antibodies
Immunohistochemistry
Hemangiopericytoma
Frozen Sections
Hematoxylin
Eosine Yellowish-(YS)
Neoplasms
Skeletal Muscle
Differential Diagnosis

Keywords

  • Cadherins
  • Lung adenocarcinoma
  • Paraffin immunohistochemistry
  • Pleural mesothelioma

ASJC Scopus subject areas

  • Pathology and Forensic Medicine

Cite this

Differential expression of N-cadherin in pleural mesotheliomas and E- cadherin in lung adenocarcinomas in formalin-fixed, paraffin-embedded tissues. / Han, Aaron C.; Peralta-Soler, Alejandro; Knudsen, Karen A.; Wheelock, Margaret J.; Johnson, Keith R.; Salazar, Hernando.

In: Human Pathology, Vol. 28, No. 6, 01.01.1997, p. 641-645.

Research output: Contribution to journalArticle

Han, Aaron C. ; Peralta-Soler, Alejandro ; Knudsen, Karen A. ; Wheelock, Margaret J. ; Johnson, Keith R. ; Salazar, Hernando. / Differential expression of N-cadherin in pleural mesotheliomas and E- cadherin in lung adenocarcinomas in formalin-fixed, paraffin-embedded tissues. In: Human Pathology. 1997 ; Vol. 28, No. 6. pp. 641-645.
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AB - The differential diagnosis of pleural mesotheliomas and lung adenocarcinomas presents a continued challenge in the practice of surgical pathology. Paraffin immunohistochemistry (IHC) using different panels of antibodies can be helpful in some cases, but, as yet, no antigen is expressed specifically in mesotheliomas nor in adenocarcinomas. Using well characterized monoclonal antibodies (MAb) that recognized distinct mesenchymal and epithelial adhesion proteins, N-cadherin (13A9 MAb) and E- cadherin (E9 MAb), respectively, we found previously that in frozen-section IHC mesotheliomas and adenocarcinomas had distinct cadherin phenotypes: mesotheliomas were positive for N-cadherin, and lung adenocarcinomas were positive for E-cadherin. Using antigen-retrieval methods, we successfully extended our study to formalin-fixed, paraffin-embedded tissue sections. Tumors from 28 patients (14 originally diagnosed as mesotheliomas, and 14 diagnosed as adenocarcinomas) were stained with 13A9 MAb and E9 MAb. Review of hematoxylin-eosin sections excluded from analysis one case previously diagnosed as mesothelioma, which represented a hemangiopericytoma. Of the remaining 27 cases, 12 of 13 mesotheliomas were positive for N-cadherin and negative for E-cadherin. The exception was a multifocal microscopic papillary tumor of apparent mesothelial origin, which was negative for both N-cadherin and E-cadherin. Conversely, 13 of 14 adenocarcinomas were E-cadherin positive and N-cadherin negative except for one adenocarcinoma with focal N-cadherin expression. One case of a poorly differentiated adenocarcinoma invading skeletal muscle was negative for both 13A9 and E9. These studies confirmed the utility of die cadherin antibodies in distinguishing pleural mesotheliomas from lung adenocarcinomas. The reactivity of the cadherin- specific antibodies with antigens in paraffin sections make them powerful and reliable markers in the practice of diagnostic surgical pathology.

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