Tischler Arthur S., Semple Joseph
Endocr Pathol. 1996 Winter;7(4):265-272. doi: 10.1007/BF02739833.
Clues to mechanisms regulating development and tumorigenesis may be provided by studies of unusual diseases. Beckwit-Wiedemann syndrome (BWS) is a rare congenital disorder apparently related to abnormal regulation of insulin-like growth factor-2 (IGF-2) production. IGF2 mRNA has been previously localized to the chief cells of extra-adrenal paraganglia and to adult, but not fetal, adrenal medulla. Expression of IGF-2 by neuroblastomas has been hypothesized to reflect extra-adrenal paraganglionic differentiation. In the adrenals of a fetus with 8W5, we have observed both increased numbers of chromaffin cells and organoid nodules resembling extra-adrenal paraganglia. Immunoreactive IGF-2 was observed in both cell types, but was also observed in chromaffin cells in the normal fetal adrenal. The findings suggest autocrine or paracrine influences of IGF-2 in regulating the number and phenotype of cells derived from sympathoadrenal precursors in the developing adrenal medulla as well as in extra-adrenal paraganglia. These results have implications for the interpretation of data from neuroblastoma studies.
对罕见疾病的研究可能会为调控发育和肿瘤发生的机制提供线索。贝克威思-维德曼综合征(BWS)是一种罕见的先天性疾病,显然与胰岛素样生长因子2(IGF-2)产生的异常调节有关。IGF2 mRNA先前已定位到肾上腺外副神经节的主细胞以及成年肾上腺髓质,但未定位到胎儿肾上腺髓质。有人推测神经母细胞瘤中IGF-2的表达反映了肾上腺外副神经节的分化。在患有8W5的胎儿肾上腺中,我们观察到嗜铬细胞数量增加以及类似肾上腺外副神经节的类器官结节。在这两种细胞类型中均观察到免疫反应性IGF-2,但在正常胎儿肾上腺的嗜铬细胞中也观察到了。这些发现表明IGF-2在调节发育中的肾上腺髓质以及肾上腺外副神经节中源自交感肾上腺前体的细胞数量和表型方面具有自分泌或旁分泌作用。这些结果对神经母细胞瘤研究数据的解释具有启示意义。