Differential expression of CD44S and hyaluronic acid in malignant mesotheliomas, adenocarcinomas, and reactive mesothelial hyperplasias

Alaa M Afify, Robert Stern, Greg Jobes, Joyce L. Bailey, Bruce A. Werness

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

Many characteristics of epithelial cells are moderated through interactions with adjacent stromal components. In tumor cells, abnormal interactions between cells and stroma can be important determinants of malignant progression, including invasion and metastasis. Evidence has accumulated for the importance of the interaction between the stromal component hyaluronic acid (HA) and its major cell surface receptor, CD44S, in invasion and metastasis. Because malignant mesotheliomas are characterized by the accumulation of abundant HA, we chose to evaluate this group of tumors for the presence of stromal HA, cellular HA, and CD44S, the CD44 molecule that is principal receptor for HA. For comparison, we also analyzed a group of lung adenocarcinomas and several reactive mesothelial hyperplasias, two entities that are often included in the differential diagnosis of malignant mesothelioma. In 10 of 12 (83%) reactive mesothelial hyperplasias, 14 of 22 (63%) mesotheliomas, and 9 of 26 (34%) adenocarcinomas, membrane immunoreactivity with CD44S could be demonstrated, a difference that was statistically significant between adenocarcinomas and reactive mesothelial hyperplasias (p = 0.0128) and approached significance between adenocarcinomas and mesotheliomas (p = 0.0810). Adenocarcinomas, when positive, were more likely to show more focal staining compared with the more common diffuse staining in mesotheliomas. Although a high percentage of samples from all three groups showed stromal HA, cellular HA was much more common in mesothelioma cells (20 of 22; 91%) than in either adenocarcinomas (4 of 26; 15%, p < 0.0001) or mesothelial hyperplasias (2 of 12; 17%, p = 0.0001). Comparison of HA staining with standard immunohistochemical markers is needed to demonstrate the diagnostic utility of this stain.

Original languageEnglish (US)
Pages (from-to)11-15
Number of pages5
JournalApplied Immunohistochemistry
Volume6
Issue number1
DOIs
StatePublished - 1998
Externally publishedYes

Fingerprint

Hyaluronic Acid
Hyperplasia
Adenocarcinoma
Mesothelioma
Staining and Labeling
Neoplasm Metastasis
Malignant Mesothelioma
Cell Surface Receptors
Cell Communication
Neoplasms
Differential Diagnosis
Coloring Agents
Epithelial Cells
Membranes

Keywords

  • Adenocarcinoma
  • CD44S
  • Hyaluronic acid
  • Malignant mesothelioma
  • Mesothelial hyperplasia

ASJC Scopus subject areas

  • Anatomy
  • Medical Laboratory Technology

Cite this

Differential expression of CD44S and hyaluronic acid in malignant mesotheliomas, adenocarcinomas, and reactive mesothelial hyperplasias. / Afify, Alaa M; Stern, Robert; Jobes, Greg; Bailey, Joyce L.; Werness, Bruce A.

In: Applied Immunohistochemistry, Vol. 6, No. 1, 1998, p. 11-15.

Research output: Contribution to journalArticle

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abstract = "Many characteristics of epithelial cells are moderated through interactions with adjacent stromal components. In tumor cells, abnormal interactions between cells and stroma can be important determinants of malignant progression, including invasion and metastasis. Evidence has accumulated for the importance of the interaction between the stromal component hyaluronic acid (HA) and its major cell surface receptor, CD44S, in invasion and metastasis. Because malignant mesotheliomas are characterized by the accumulation of abundant HA, we chose to evaluate this group of tumors for the presence of stromal HA, cellular HA, and CD44S, the CD44 molecule that is principal receptor for HA. For comparison, we also analyzed a group of lung adenocarcinomas and several reactive mesothelial hyperplasias, two entities that are often included in the differential diagnosis of malignant mesothelioma. In 10 of 12 (83{\%}) reactive mesothelial hyperplasias, 14 of 22 (63{\%}) mesotheliomas, and 9 of 26 (34{\%}) adenocarcinomas, membrane immunoreactivity with CD44S could be demonstrated, a difference that was statistically significant between adenocarcinomas and reactive mesothelial hyperplasias (p = 0.0128) and approached significance between adenocarcinomas and mesotheliomas (p = 0.0810). Adenocarcinomas, when positive, were more likely to show more focal staining compared with the more common diffuse staining in mesotheliomas. Although a high percentage of samples from all three groups showed stromal HA, cellular HA was much more common in mesothelioma cells (20 of 22; 91{\%}) than in either adenocarcinomas (4 of 26; 15{\%}, p < 0.0001) or mesothelial hyperplasias (2 of 12; 17{\%}, p = 0.0001). Comparison of HA staining with standard immunohistochemical markers is needed to demonstrate the diagnostic utility of this stain.",
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