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肾细胞癌骨转移

Bone Metastasis from Renal Cell Carcinoma.

作者信息

Chen Szu-Chia, Kuo Po-Lin

机构信息

Graduate Institute of Clinical Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.

Division of Nephrology, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung 807, Taiwan.

出版信息

Int J Mol Sci. 2016 Jun 22;17(6):987. doi: 10.3390/ijms17060987.

Abstract

About one-third of patients with advanced renal cell carcinoma (RCC) have bone metastasis that are often osteolytic and cause substantial morbidity, such as pain, pathologic fracture, spinal cord compression and hypercalcemia. The presence of bone metastasis in RCC is also associated with poor prognosis. Bone-targeted treatment using bisphosphonate and denosumab can reduce skeletal complications in RCC, but does not cure the disease or improve survival. Elucidating the molecular mechanisms of tumor-induced changes in the bone microenvironment is needed to develop effective treatment. The "vicious cycle" hypothesis has been used to describe how tumor cells interact with the bone microenvironment to drive bone destruction and tumor growth. Tumor cells secrete factors like parathyroid hormone-related peptide, transforming growth factor-β and vascular endothelial growth factor, which stimulate osteoblasts and increase the production of the receptor activator of nuclear factor κB ligand (RANKL). In turn, the overexpression of RANKL leads to increased osteoclast formation, activation and survival, thereby enhancing bone resorption. This review presents a general survey on bone metastasis in RCC by natural history, interaction among the immune system, bone and tumor, molecular mechanisms, bone turnover markers, therapies and healthcare burden.

摘要

约三分之一的晚期肾细胞癌(RCC)患者会发生骨转移,这些转移灶通常为溶骨性,会导致严重的发病情况,如疼痛、病理性骨折、脊髓压迫和高钙血症。RCC患者出现骨转移也与预后不良相关。使用双膦酸盐和地诺单抗进行骨靶向治疗可减少RCC的骨骼并发症,但无法治愈疾病或提高生存率。需要阐明肿瘤诱导骨微环境变化的分子机制以开发有效的治疗方法。“恶性循环”假说已被用于描述肿瘤细胞如何与骨微环境相互作用以驱动骨破坏和肿瘤生长。肿瘤细胞分泌甲状旁腺激素相关肽、转化生长因子-β和血管内皮生长因子等因子,这些因子刺激成骨细胞并增加核因子κB受体活化因子配体(RANKL)的产生。反过来,RANKL的过度表达导致破骨细胞形成、活化和存活增加,从而增强骨吸收。本文综述了RCC骨转移的自然史、免疫系统、骨与肿瘤之间的相互作用、分子机制、骨转换标志物、治疗方法及医疗负担等方面的概况。

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