Powers James F, Picard Kristen L, Nyska Abraham, Tischler Arthur S
Department of Pathology, Tufts-New England Medical Center, Boston, MA 02111, USA.
Endocr Pathol. 2008 Spring;19(1):9-16. doi: 10.1007/s12022-008-9019-1.
Pheochromocytomas are catecholamine-producing tumors of the adult adrenal medulla. They are rare in humans and most other species but common in laboratory rats. However, the relevance of rat pheochromocytomas as a model for their human counterparts is uncertain. Previous studies of spontaneous and drug-induced rat pheochromocytomas and the PC12 pheochromocytoma cell line suggested a distinctive noradrenergic phenotype, possibly reflecting origin from a progenitor not present in the adult human adrenal. In this study, we studied 31 pheochromocytomas derived from test and control male and female rats in toxicologic studies for expression of the epinephrine-synthesizing enzyme phenylethanolamine-N-methyltransferase (PNMT) and the receptor tyrosine kinase Ret. PNMT, which defines adrenergic chromaffin cells, is frequently expressed in human pheochromocytomas, often in tumors that also overexpress RET. We also tested for the expression of the cell cycle checkpoint protein p27(Kip1), which recently was reported absent in pheochromocytomas from a strain of rats with a hereditary mixed multiple endocrine neoplasia (MEN)-like syndrome. Using immunoblots, we demonstrated PNMT expression in almost 50% of the 31 tumors, although often at lower levels than in normal rat adrenal medulla. The majority of tumors overexpressed Ret. There was no apparent correlation between PNMT and Ret. However, in this study, PNMT expression was strongly associated with tumors arising in female rats, while overexpression of Ret did not show a sex predilection. Robust expression of p27(Kip1) was seen in all tumors from the toxicologic studies and also in a small sample of pheochromocytomas from Long-Evans rats, which were reported to have a mixed MEN-like syndrome in the 1980s. The present results show that rat pheochromocytomas have greater phenotypic diversity than previously believed and greater similarity to their human counterparts with respect to these two important markers. Loss of p27(Kip1) does not appear to account for the high frequency of pheochromocytomas in commonly utilized rat strains.
嗜铬细胞瘤是成人肾上腺髓质产生儿茶酚胺的肿瘤。它们在人类和大多数其他物种中很少见,但在实验大鼠中很常见。然而,大鼠嗜铬细胞瘤作为人类嗜铬细胞瘤模型的相关性尚不确定。先前对自发性和药物诱导的大鼠嗜铬细胞瘤以及PC12嗜铬细胞瘤细胞系的研究表明,其具有独特的去甲肾上腺素能表型,这可能反映了其起源于成年人类肾上腺中不存在的祖细胞。在本研究中,我们研究了来自毒理学研究中试验组和对照组雄性及雌性大鼠的31个嗜铬细胞瘤,以检测肾上腺素合成酶苯乙醇胺 - N - 甲基转移酶(PNMT)和受体酪氨酸激酶Ret的表达。定义肾上腺素能嗜铬细胞的PNMT在人类嗜铬细胞瘤中经常表达,通常在同时过表达RET的肿瘤中表达。我们还检测了细胞周期检查点蛋白p27(Kip1)的表达,最近有报道称,在患有遗传性混合性多内分泌腺瘤(MEN)样综合征的大鼠品系的嗜铬细胞瘤中不存在该蛋白。使用免疫印迹法,我们在31个肿瘤中的近50%中证实了PNMT的表达,尽管其水平通常低于正常大鼠肾上腺髓质。大多数肿瘤过表达Ret。PNMT和Ret之间没有明显的相关性。然而,在本研究中,PNMT的表达与雌性大鼠产生的肿瘤密切相关,而Ret的过表达没有显示出性别偏好。在毒理学研究的所有肿瘤以及一小部分来自Long - Evans大鼠的嗜铬细胞瘤样本中都观察到了p27(Kip1)的强表达,据报道,Long - Evans大鼠在20世纪80年代患有混合性MEN样综合征。目前的结果表明,大鼠嗜铬细胞瘤的表型多样性比以前认为的更大,并且在这两个重要标志物方面与人类嗜铬细胞瘤更相似。p27(Kip1)的缺失似乎并不能解释常用大鼠品系中嗜铬细胞瘤的高发病率。