Ke. Schoedel et al., EXPRESSION OF METALLOPROTEINASES AND TISSUE INHIBITOR IN CARTILAGINOUS NEOPLASMS OF BONE, Applied immunohistochemistry, 5(2), 1997, pp. 111-116
Difficulties may be encountered when attempting to histologically diff
erentiate a low-grade chondrosarcoma from the benign enchondroma. Beca
use many malignant neoplasms demonstrate an imbalance between metallop
roteinases and tissue inhibitors of metalloproteinases, we compared th
e expression of these markers in benign enchondromas and chondrosarcom
as of bone. Eight enchondromas and 11 chondrosarcomas of the long bone
s (six grade 1, two grade 2, and three grade 3) were collected from th
e files of the Department of Pathology at the Hospital for Joint Disea
ses. Immunohistochemistry was performed on paraffin-embedded tissue us
ing antibodies to metalloproteinases (MMP-1, MMP-2, MMP-9) and a tissu
e inhibitor of MMP (TIMP-1). Both enchondromas and chondrosarcomas sho
wed cytoplasmic immunoreactivity for MMP-1 and MMP-2 in the neoplastic
chondroid cells. Furthermore, when the extracellular matrix was evalu
ated, nine chondrosarcomas demonstrated matrix staining for MMP-1 as d
id eight chondrosarcomas for MMP-2. However, none of the eight enchond
romas showed matrix reactivity for MMP-1 or MMP-2. Six enchondromas an
d 10 chondrosarcomas showed cytoplasmic positivity for MMP-9. Matrix s
taining for MMP-9 was observed in two enchondromas and six chondrosarc
omas. Cytoplasmic staining for TIMP-1 was present in all cases. Matrix
staining for TIMP-1 was seen in seven chondrosarcomas and one enchond
roma. The expression of metalloproteinases and tissue inhibitors of me
talloproteinases may have a role in influencing the behavior of chondr
oid neoplasms. However, the presence of MMP-1, MMP-2, and TIMP-1 in th
e extracellular matrix of chondrosarcomas and the increased expression
of MMP-9 in chondrosarcoma as compared with enchondroma suggest abnor
mal regulation in their expression and may be useful markers in distin
guishing benign from malignant chondroid lesions.