Hepatocellular carcinoma with osteoclast-like giant cells: Possibility of osteoclastogenesis by hepatocyte-derived cells

被引:31
作者
Ikeda, T
Seki, S
Maki, M
Noguchi, N
Kawamura, T
Arii, S
Igari, T
Koike, M
Hirokawa, K
机构
[1] Tokyo Med & Dent Univ, Grad Sch, Dept Pathol & Immunol, Tokyo 1138519, Japan
[2] Tokyo Med & Dent Univ, Grad Sch, Dept Hepatobiliary Surg, Tokyo 1138519, Japan
[3] Tokyo Med & Dent Univ, Grad Sch, Dept Human Pathol, Tokyo 1138519, Japan
[4] Showa Univ, Sch Med, Dept Pathol 1, Tokyo 142, Japan
[5] Tokyo Med & Dent Univ Hosp, Dept Surg Pathol, Tokyo, Japan
关键词
hepatocellular carcinoma; osteoclastogenesis; receptor activator of nuclear factor kappa B; receptor activator of nuclear factor kappa B ligand;
D O I
10.1046/j.1440-1827.2003.01503.x
中图分类号
R36 [病理学];
学科分类号
100104 [病理学与病理生理学];
摘要
Giant cell tumor (GCT) of bone is a primary osteolytic tumor that is characterized by the formation of osteoclast-like giant cells. In addition to GCT of bone, extraskeletal GCT are known to be formed in several soft tissues. Giant cells in GCT of bone were suggested to be identical to osteoclasts, but the characterization of giant cells in extraskeletal GCT remains incomplete. In this study, a case of sarcomatoid hepatocellular carcinoma with osteoclast-like giant cells was analyzed. Immunohistochemistry revealed the expression of almost all markers of osteoclasts: tartrate-resistant acid phosphatase, CD68, CD51, CD54 and matrix metalloprotease-9, in osteoclast-like giant cells in the tumor. In situ hybridization revealed the expression of receptor activator of nuclear factor-kappa B (RANK) in the giant cells and receptor activator of nuclear factor-kappa B ligand (RANKL) in the tumor cells. The hepatic origin of the sarcomatoid hepatocellular carcinoma cells was confirmed by the expression of albumin. This is the first report suggesting that hepatocyte-derived cells possess the potential for osteoclastogenesis. In addition, these findings suggest that osteoclast-like cells in the hepatocellular carcinoma were formed by the same mechanism as osteoclastogenesis in bone.
引用
收藏
页码:450 / 456
页数:7
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