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Reciprocal changes in the expression of transcription factors GATA-4 and GATA-6 accompany adrenocortical tumorigenesis in mice and humans.

机译:转录因子GATA-4和GATA-6表达的相互变化伴随着小鼠和人类的肾上腺皮质肿瘤发生。

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摘要

While certain genetic changes are frequently found in adrenocortical carcinoma cells, the molecular basis of adrenocortical tumorigenesis remains poorly understood. Given that the transcription factors GATA-4 and GATA-6 have been implicated in gene expression and cellular differentiation in a variety of tissues, including endocrine organs such as testis, we have now examined their expression in the developing adrenal gland, as well as in adrenocortical cell lines and tumors from mice and humans. Northern blot analysis and in situ hybridization revealed abundant GATA-6 mRNA in the fetal and postnatal adrenal cortex of the mouse. In contrast, little or no GATA-4 expression was detected in adrenal tissue during normal development. In vivo stimulation with ACTH or suppression with dexamethasone did not affect the expression of GATA-4 or GATA-6 in the murine adrenal gland. To assess whether changes in the expression of GATA-4 or GATA-6 accompany adrenocortical tumorigenesis, we employed an established mouse model. When gonadectomized, inhibin alpha/SV40 T-antigen transgenic mice develop adrenocortical tumors in a gonadotropin-dependent fashion. In striking contrast to the normal adrenal glands, GATA-6 mRNA was absent from adrenocortical tumors or tumor-derived cell lines, while GATA-4 mRNA and protein were abundantly expressed in the tumors and tumor cell lines. Analogous results were obtained with human tissue samples; GATA-4 expression was detected in human adrenocortical carcinomas but not in normal tissue, adenomas, or pheochromocytomas. Taken together these results suggest different roles for GATA-4 and GATA-6 in the adrenal gland, and implicate GATA-4 in adrenal tumorigenesis. Immunohistochemical detection of GATA-4 may serve as a useful marker in the differential diagnosis of human adrenal tumors.
机译:尽管在肾上腺皮质癌细胞中经常发现某些遗传变化,但对肾上腺皮质肿瘤发生的分子基础仍然知之甚少。鉴于转录因子GATA-4和GATA-6与多种组织(包括内分泌器官,如睾丸)的基因表达和细胞分化有关,因此我们现在研究了它们在发育中的肾上腺以及在肾上腺中的表达。小鼠和人类的肾上腺皮质细胞系和肿瘤。 Northern印迹分析和原位杂交揭示了小鼠的胎儿和出生后肾上腺皮质中丰富的GATA-6 mRNA。相反,在正常发育过程中在肾上腺组织中几乎没有检测到GATA-4表达。 ACTH的体内刺激或地塞米松的抑制作用不影响鼠肾上腺中GATA-4或GATA-6的表达。为了评估GATA-4或GATA-6表达的变化是否伴随肾上腺皮质肿瘤发生,我们采用了已建立的小鼠模型。淋巴切除后,抑制素α/ SV40 T-抗原转基因小鼠以促性腺激素依赖性方式发展肾上腺皮质肿瘤。与正常的肾上腺形成鲜明对比的是,肾上腺皮质肿瘤或肿瘤衍生的细胞系中没有GATA-6 mRNA,而在肿瘤和肿瘤细胞系中GATA-4 mRNA和蛋白大量表达。用人体组织样品获得了相似的结果。在人肾上腺皮质癌中检测到GATA-4表达,但在正常组织,腺瘤或嗜铬细胞瘤中未检测到。总之,这些结果表明GATA-4和GATA-6在肾上腺中的不同作用,并暗示了GATA-4在肾上腺肿瘤发生中的作用。 GATA-4的免疫组织化学检测可作为鉴别人类肾上腺肿瘤的有用标志物。

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