骨保护素
兰克尔
骨转移
医学
转移
免疫组织化学
前列腺癌
原发性肿瘤
初生骨
骨重建
激活剂(遗传学)
病理
肿瘤科
受体
内科学
癌症研究
癌症
作者
Daniele Santini,Giuseppe Perrone,Ilaria Roato,Laura Godio,Francesco Pantano,Donatella Grasso,Antonio Russo,Bruno Vincenzi,Maria Elisabetta Fratto,Roberto Sabbatini,Chiara Della Pepa,Camillo Porta,Alessandro Del Conte,Gaia Schiavon,Alfredo Berruti,Rosa Maria Tomasino,Mauro Papotti,Nicola Papapietro,Andrea Onetti Muda,Vincenzo Denaro,Giuseppe Tonini
摘要
Abstract Receptor activator of NFκB ligand (RANKL), RANK, and osteoprotegerin (OPG) represent the key regulators of bone metabolism both in normal and pathological conditions, including bone metastases. To our knowledge, no previous studies investigated and compared RANK expression in primary tumors and in bone metastases from the same patient. We retrospectively examined RANK expression by immunohistochemistry in 74 bone metastases tissues from solid tumors, mostly breast, colorectal, renal, lung, and prostate cancer. For 40 cases, tissue from the corresponding primary tumor was also analyzed. Sixty‐six (89%) of the 74 bone metastases were RANK‐positive and, among these, 40 (59.5%) showed more than 50% of positive tumor cells. The median percentage of RANK‐positive cells was 60% in primary tumors and metastases, without any statistically significant difference between the two groups ( P = 0.194). The same percentage was obtained by considering only cases with availability of samples both from primary and metastasis. Our study shows that RANK is expressed by solid tumors, with high concordance between bone metastasis and corresponding primary tumor. These data highlight the central role of RANK/RANKL/OPG pathway as potential therapeutic target not only in bone metastasis management, but also in the adjuvant setting. J. Cell. Physiol. 226: 780–784, 2011. © 2010 Wiley‐Liss, Inc.
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