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Expression of hydroxyindole-O-methyltransferase enzyme in the human central nervous system and in pineal parenchymal cell tumors.

Abstract
Pineal parenchymal tumor (PPT) cells usually show immunoreactivity for synaptophysin, neuron-specific enolase, neurofilament protein, class III beta-tubulin, tau protein, PGP9.5, chromogranin, serotonin, retinal S-antigen, and rhodopsin, but these markers are not specific for PPTs. Melatonin is produced and secreted mainly bypineal parenchymal cells; hydroxyindole-O-methyltransferase (HIOMT) catalyzes the final reaction in melatonin biosynthesis. We hypothesized that HIOMT could serve as a tumor marker of PPTs, and we investigated HIOMT localization and HIOMT expression in samples of normal human tissue and in PPTs, primitive neuroectodermal tumors, and medulloblastomas. In normal tissue, HIOMT was expressed in retinal cells, pineal parenchymal cells, neurons of the Edinger-Westphal nucleus, microglia, macrophages, thyroid follicular epithelium, principal and oxyphil cells of parathyroid gland, adrenal cortical cells, hepatic parenchymal cells, renal tubule epithelium, and enteroendocrine cells of stomach and duodenum. The HIOMT was also expressed in all 46 PPTs studied. The proportions of HIOMT-immunoreactive cells successively decreased in the following tumors: pineocytoma, pineal parenchymal tumor of intermediate differentiation, and pineoblastoma. A few HIOMT-immunoreactive cells were observed in one of 6 primitive neuroectodermal tumors and 23 of 42 medulloblastomas. These results indicate that HIOMT immunohistochemistry may be useful for the diagnosis of PPTs and be a prognostic factor in PPTs.
AuthorsTakahiro Fukuda, Nobutake Akiyama, Masahiro Ikegami, Hitoshi Takahashi, Atsushi Sasaki, Hidehiro Oka, Takashi Komori, Yuko Tanaka, Youichi Nakazato, Jiro Akimoto, Masahiko Tanaka, Yoshikazu Okada, Saburo Saito
JournalJournal of neuropathology and experimental neurology (J Neuropathol Exp Neurol) Vol. 69 Issue 5 Pg. 498-510 (May 2010) ISSN: 1554-6578 [Electronic] England
PMID20418777 (Publication Type: Journal Article)
Chemical References
  • Arrestin
  • Eye Proteins
  • Nerve Tissue Proteins
  • Plant Lectins
  • RNA, Messenger
  • Ricinus communis agglutinin-1
  • enhanced green fluorescent protein
  • Green Fluorescent Proteins
  • Acetylserotonin O-Methyltransferase
Topics
  • Acetylserotonin O-Methyltransferase (genetics, metabolism)
  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Animals
  • Arrestin (metabolism)
  • Brain Neoplasms (pathology)
  • Cell Line, Tumor
  • Central Nervous System (enzymology, pathology)
  • Child
  • Child, Preschool
  • Eye Proteins (genetics, metabolism)
  • Female
  • Green Fluorescent Proteins (genetics)
  • Humans
  • Infant
  • Male
  • Middle Aged
  • Nerve Tissue Proteins (metabolism)
  • Neurons (metabolism)
  • Pineal Gland (pathology)
  • Pinealoma (pathology)
  • Plant Lectins (metabolism)
  • RNA, Messenger (metabolism)
  • Retina (pathology)
  • Transfection (methods)

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