Hosokawa Y, Pollak M R, Brown E M, Arnold A
Endocrine Oncology Laboratory, Massachusetts General Hospital, Boston 02114, USA.
J Clin Endocrinol Metab. 1995 Nov;80(11):3107-10. doi: 10.1210/jcem.80.11.7593409.
Despite recent progress, such as the identification of PRAD1/cyclin D1 as a parathyroid oncogene, it is likely that many genes involved in the molecular pathogenesis of parathyroid tumors remain unknown. Individuals heterozygous for inherited mutations in the extracellular Ca(2+)-sensing receptor gene that reduce its biological activity exhibit a disorder termed familial hypocalciuric hypercalcemia or familial benign hypercalcemia, which is characterized by reduced responsiveness of parathyroid and kidney to calcium and by PTH-dependent hypercalcemia. Those who are homozygous for such mutations present with neonatal severe hyperparathyroidism and have marked parathyroid hypercellularity. Thus, the Ca(2+)-sensing receptor gene is a candidate parathyroid tumor suppressor gene, with inactivating mutations plausibly explaining set-point abnormalities in the regulation of both parathyroid cellular proliferation and PTH secretion by extracellular Ca2+ similar to those seen in hyperparathyroidism. Using a ribonuclease A protection assay that has detected multiple mutations in the Ca(2+)-sensing receptor gene in familial hypocalciuric hypercalcemia and covers more than 90% of its coding region, we sought somatic mutations in this gene in a total of 44 human parathyroid tumors (23 adenomas, 4 carcinomas, 5 primary hyperplasias, and 12 secondary hyperplasias). No such mutations were detected in these 44 tumors. Thus, our studies suggest that somatic mutation of the Ca(2+)-sensing receptor gene does not commonly contribute to the pathogenesis of sporadic parathyroid tumors. As such, PTH set-point dysfunction in parathyroid tumors may well be secondary to other clonal proliferative defects and/or mutations in other components of the extracellular Ca(2+)-sensing pathway.
尽管最近取得了一些进展,比如将PRAD1/细胞周期蛋白D1鉴定为甲状旁腺癌基因,但参与甲状旁腺肿瘤分子发病机制的许多基因可能仍然未知。细胞外Ca(2+) 传感受体基因发生遗传性突变的杂合个体,其生物活性降低,表现出一种称为家族性低钙血症性高钙血症或家族性良性高钙血症的病症,其特征是甲状旁腺和肾脏对钙的反应性降低以及甲状旁腺激素依赖性高钙血症。那些此类突变纯合的个体表现为新生儿严重甲状旁腺功能亢进,且甲状旁腺细胞明显增多。因此,Ca(2+) 传感受体基因是甲状旁腺肿瘤抑制基因的候选者,其失活突变可能解释了甲状旁腺细胞增殖和细胞外Ca2+ 对甲状旁腺激素分泌调节中的设定点异常,类似于甲状旁腺功能亢进中所见的情况。我们使用一种核糖核酸酶A保护试验,该试验已在家族性低钙血症性高钙血症中检测到Ca(2+) 传感受体基因的多个突变,且覆盖了其编码区域的90% 以上,我们在总共44个人类甲状旁腺肿瘤(23个腺瘤、4个癌、5个原发性增生和12个继发性增生)中寻找该基因的体细胞突变。在这44个肿瘤中未检测到此类突变。因此,我们的研究表明,Ca(2+) 传感受体基因的体细胞突变通常不参与散发性甲状旁腺肿瘤的发病机制。因此,甲状旁腺肿瘤中的甲状旁腺激素设定点功能障碍很可能继发于其他克隆性增殖缺陷和/或细胞外Ca(2+) 传感途径其他成分的突变。