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恶性肿瘤体液性高钙血症:关于临床特征的一些谜团。

Humoral hypercalcemia of malignancy: some enigmas on the clinical features.

作者信息

Ikeda K, Ogata E

机构信息

Fourth Department of Internal Medicine, University of Tokyo School of Medicine, Japan.

出版信息

J Cell Biochem. 1995 Mar;57(3):384-91. doi: 10.1002/jcb.240570303.

Abstract

Humoral hypercalcemia of malignancy (HHM) is a common paraneoplastic syndrome mediated by tumor-derived parathyroid hormone-related peptide (PTHRP), which bears structural and functional similarities to PTH. Thus the clinical features of HHM are very similar to those of primary hyperparathyroidism (1 degree HPT), a prototype of humoral hypercalcemia caused by PTH. On the other hand, HHM syndrome differs from 1 degree HPT in several aspects, including serum 1,25(OH)2D levels, acid-base balance, and bone remodeling process, the reason of which remains largely unknown. We approached these questions using a unique animal model of HHM, nude rats implanted with PTHRP-overproducing human carcinomas. In this review we will summarize the results and discuss the implications in understanding the disease mechanism.

摘要

恶性肿瘤体液性高钙血症(HHM)是一种常见的副肿瘤综合征,由肿瘤衍生的甲状旁腺激素相关肽(PTHRP)介导,该肽与甲状旁腺激素(PTH)在结构和功能上相似。因此,HHM的临床特征与原发性甲状旁腺功能亢进症(1度HPT)非常相似,原发性甲状旁腺功能亢进症是由PTH引起的体液性高钙血症的典型代表。另一方面,HHM综合征在几个方面与1度HPT不同,包括血清1,25(OH)2D水平、酸碱平衡和骨重塑过程,其原因在很大程度上仍然未知。我们使用一种独特的HHM动物模型来解决这些问题,即植入产生PTHRP的人类癌细胞的裸鼠。在这篇综述中,我们将总结结果并讨论其对理解疾病机制的意义。

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