Y. Oda et al., IMMUNOHISTOCHEMICAL ANALYSIS OF NM23 PROTEIN EXPRESSION IN MALIGNANT BONE-TUMORS, Journal of cancer research and clinical oncology, 121(11), 1995, pp. 667-673
Expression levels of nm23 protein in 72 malignant bone tumors comprisi
ng 41 osteosarcomas, 22 chondrosarcomas, 6 Ewing's sarcomas, and 2 mal
ignant fibrous histiocytomas were examined immunohistochemically, usin
g anti-nm23 protein polyclonal antibody, and compared with 51 cases of
benign bone tumors or tumor-like lesions. Malignant bone tumors showe
d significantly higher nm23 protein expression than benign bone tumors
or tumor-like lesions (P <0.0001). In chondrosarcoma, nm23 expression
increased in high-grade tumors (grade I versus grade II and III: P =
0.0229). In the cases of osteosarcoma, however, grade IV osteosarcomas
showed decreased expression of nm23 compared with grade III tumors (P
= 0.0122). There was no significant relationship between nm23 express
ion and histological type. nm23 expression had no correlation with met
astatic potential in osteosarcoma, although the therapy was not unifor
m in our cases. Furthermore, in 6 cases of osteosarcoma and 1 case of
Ewing's sarcoma, there was no clear tendency for a decrease of nm23 in
the metastatic sites compared with primary sites, as reported in brea
st cancer. These results showed that, in contrast to reports on breast
cancer and experimental models, nm23 protein expression in human bone
tumors may be associated with malignant potentiality, except in cases
of osteosarcoma.