Laboratory of Experimental Endocrinology, IRCCS Istituto Ortopedico Galeazzi, 20161 Milan, Italy.
Department of Biomedical, Surgical and Dental Sciences, University of Milan, 20122 Milan, Italy.
Int J Mol Sci. 2021 Feb 18;22(4):2016. doi: 10.3390/ijms22042016.
The Hippo pathway is involved in human tumorigenesis and tissue repair. Here, we investigated the Hippo coactivator Yes-associated protein 1 (YAP1) and the kinase large tumor suppressor 1/2 (LATS1/2) in tumors of the parathyroid glands, which are almost invariably associated with primary hyperparathyroidism. Compared with normal parathyroid glands, parathyroid adenomas (PAds) and carcinomas show variably but reduced nuclear YAP1 expression. The kinase LATS1/2, which phosphorylates YAP1 thus promoting its degradation, was also variably reduced in PAds. Further, silencing reduces the expression of the key parathyroid oncosuppressor , while silencing increases expression. Treatment of patient-derived PAds-primary cell cultures and Human embryonic kidney 293A (HEK293A) cells expressing the calcium-sensing receptor (CASR) with the CASR agonist R568 induces YAP1 nuclear accumulation. This effect was prevented by the incubation of the cells with RhoA/Rho-associated coiled-coil-containing protein kinase (ROCK) inhibitors Y27632 and H1152. Lastly, CASR activation increased the expression of the YAP1 gene targets , , and , and this effect was blunted by silencing. Concluding, here we provide preliminary evidence of the involvement of the Hippo pathway in human tumor parathyroid cells and of the existence of a CASR-ROCK-YAP1 axis. We propose a tumor suppressor role for YAP1 and LATS1/2 in parathyroid tumors.
Hippo 通路参与人类肿瘤发生和组织修复。在这里,我们研究了 Hippo 共激活因子 Yes 相关蛋白 1(YAP1)和激酶大肿瘤抑制因子 1/2(LATS1/2)在甲状旁腺肿瘤中的作用,这些肿瘤几乎总是与原发性甲状旁腺功能亢进有关。与正常甲状旁腺相比,甲状旁腺瘤(PAd)和癌显示出不同程度但减少的核 YAP1 表达。磷酸化 YAP1 从而促进其降解的激酶 LATS1/2 在 PAd 中也不同程度减少。此外,沉默会降低关键的甲状旁腺癌抑制基因的表达,而沉默会增加其表达。用钙敏感受体(CASR)激动剂 R568 处理源自患者的 PAd-原代细胞培养物和人胚肾 293A(HEK293A)细胞,可诱导 YAP1 核积累。该效应可通过用 RhoA/Rho 相关卷曲螺旋蛋白激酶(ROCK)抑制剂 Y27632 和 H1152 孵育细胞来预防。最后,CASR 激活增加了 YAP1 基因靶标、、和的表达,而沉默会削弱这种作用。总之,我们在这里提供了 Hippo 通路参与人类肿瘤甲状旁腺细胞以及存在 CASR-ROCK-YAP1 轴的初步证据。我们提出 YAP1 和 LATS1/2 在甲状旁腺瘤中的肿瘤抑制作用。