Characteristic features of disseminated carcinomatosis of the bone marrow due to gastric cancer: The pathogenesis of bone destruction

被引:2
|
作者
Kusumoto, Hiroki
Haraguchi, Masaru
Nozuka, Yoko
Oda, Yoshinao
Tsuneyoshi, Masazumi
Iguchi, Haruo
机构
[1] Kyushu Natl Canc Ctr, Div Gastroenterol Surg, Fukuoka, Japan
[2] Kyushu Univ, Fac Med, Dept Anat Pathol, Fukuoka 812, Japan
[3] Kyushu Natl Canc Ctr, Res Inst, Div Tumor Dynam, Fukuoka, Japan
关键词
gastric cancer; bone marrow invasion; bone destruction; receptor activator of NF-kappa B ligand;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Disseminated carcinimatosis of the bone marrow is accompanied by solid tumors, and gastric cancer accounts for the majority. The prognosis of this condition is poor, however, the pathogenesis for wide-spread bone lesions has yet to be elucidated. In 9 patients with gastric cancer demonstrating disseminated carcinomatosis of the bone marrow, the characteristic clinicopathological features were examined. Immunohistochemistry for receptor activator of NF-kappa B ligand (RANKL) and parathyroid hormone-related protein was also performed on gastric cancer tissue and bone marrow specimens to identify the factors responsible for the occurrence of bone lesions in patients presenting with this condition. The characteristic features of disseminated carcinomatosis of the bone marrow due to gastric cancer include a yonger patient age, an elevation of serum alkaline phosphatase and/or lactate dehydrogenase levels, wide-spread bone metastases with osteolytic bone destruction, a low incidence of hypercalcemia and a histological gastric cancer type of either signet ring cell carcinoma or poorly diffentiated adenocarcinoma. The expression of RANKL, which is one of the master regulators of osteoclastic bone resorption in bone metastasis, was also found in gastric cancer cells obtained from such patients. The RANKL expressed in gastric cancer may therefore play a critical role in the promotion of osteoclast fort-nation, which has been suggested to be involved in the pathogenesis of bone lesions.
引用
收藏
页码:735 / 740
页数:6
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