Expression of Amphiregulin in Enchondromas and Central Chondrosarcomas

Authors

DOI:

https://doi.org/10.6061/clinics/2021/e2914

Keywords:

Bone Tumors, Amphiregulin, Enchondroma, Chondrosarcoma, Immunohistochemistry

Abstract

OBJECTIVES: The aim of this study was to evaluate the role of amphiregulin protein, an epidermal growth factor receptor ligand, in cartilaginous tumors.

METHODS: Amphiregulin expression was examined in 31 enchondromas and 67 chondrosarcomas using immunohistochemistry analysis.

RESULTS: Overall, 15 enchondromas (48.40%) and 24 chondrosarcomas (35.82%) were positive for amphiregulin. According to the receiver operating characteristic curve test, no difference in amphiregulin expression was observed between enchondromas and low-grade chondrosarcomas (p=0.0880). Additionally, 39 lesions (16 in short bones, 13 in long bones, and 10 in flat bones) were positive for amphiregulin, exhibiting a higher percentage of positive cells (p=0.0030) and intensity of immunohistochemical expression (p=0.0055) in short bone lesions than in others. Among 25 enchondromas localized in short bones, 15 expressed amphiregulin; however, all 6 cases localized in long bones were negative for this marker (p=0.0177).

CONCLUSIONS: Amphiregulin did not help in distinguishing enchondromas from low-grade chondrosarcomas. The present study is the first to document the expression of this immunohistochemical marker in enchondromas. Furthermore, amphiregulin expression in enchondromas was localized in short bones, indicating a phenotypic distinction from that in long bones. This distinction may contribute to an improved understanding of the pathogenesis of these lesions.

Downloads

Download data is not yet available.

Downloads

Published

2021-08-27

Issue

Section

Original Articles

How to Cite

Losada, D. M., Ribeiro, A. L. da C., Cintra, F. F., Mendonça, G. R. A. de, Etchebehere, M., & Amstalden, E. M. I. (2021). Expression of Amphiregulin in Enchondromas and Central Chondrosarcomas. Clinics, 76, e2914. https://doi.org/10.6061/clinics/2021/e2914