Mendelsohn G, Baylin S B, Eggleston J C
Cancer. 1980 Feb;45(3):498-502. doi: 10.1002/1097-0142(19800201)45:3<498::aid-cncr2820450314>3.0.co;2-r.
Immunoperoxidase studies have been utilized to investigate further the previously reported presence of immunoassayable calcitonin in pheochromocytoma tissue from some patients with MEN II syndromes. We have been able to demonstrate calcitonin in pheochromocytoma tissue only in two patients with MEN II syndromes in whom the pheochromocytomas contained metastatic medullary thyroid carcinoma. In both cases, the calcitonin was present only in the medullary carcinoma. We have not been able to demonstrate immunoreactive calcitonin in normal adrenal glands or in pheochromocytomas of other patients with and without MEN syndromes. Adrenal medullary cells and thyroid C cells are both of neural crest origin and both possess APUD characteristics. The presence of calcitonin in medullary thyroid carcinoma cells and not in pheochromocytes has important implications with regard to cellular differentiation and peptide hormone production.
免疫过氧化物酶研究已被用于进一步调查先前报道的某些患有MEN II综合征患者的嗜铬细胞瘤组织中可免疫测定的降钙素的存在情况。我们仅在两名患有MEN II综合征且嗜铬细胞瘤含有转移性甲状腺髓样癌的患者的嗜铬细胞瘤组织中证实了降钙素的存在。在这两个病例中,降钙素仅存在于髓样癌中。我们未能在正常肾上腺或其他患有或未患有MEN综合征患者的嗜铬细胞瘤中证实免疫反应性降钙素的存在。肾上腺髓质细胞和甲状腺C细胞均起源于神经嵴,且都具有APUD特性。甲状腺髓样癌细胞中存在降钙素而嗜铬细胞中不存在,这对于细胞分化和肽类激素产生具有重要意义。