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PMID: 3185287 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

DNA polymerase beta in human thyroid of Graves' disease and thyroid tumors.

Metabolism: clinical and experimental ·Vol. 37 ·No. 11 ·1988-11-00 ·Pages 1051-4

Nagasaka A, Yoshida S, Nakai A, Ohyama T, Iwase K, Ohtani S, Shinoda S, Masunaga R, Nakagawa H

Abstract

We have shown that the level of DNA polymerase beta of rat adrenal cortex is regulated by pituitary trophic hormones and may correlate with their endocrine function. Here we measured DNA polymerase beta activity in human thyroid tissues of various benign and malignant thyroid disorders in order to verify the correlation between DNA polymerase beta activity and endocrine function. In Graves' disease (hyperfunction), the level of DNA polymerase beta per cell was three times higher than in normal thyroid, while in undifferentiated thyroid carcinomas this enzyme level was lower than normal. Furthermore, DNA polymerase beta in the crude extracts of cancer cells showed larger molecular forms, ranging from five to 12S, upon sucrose gradient sedimentation. These observations further support the hypothesis that the activity of DNA polymerase beta correlates, in part, with the functional level of the endocrine organ and with cell differentiation.

MeSH Terms
Adenoma/enzymology,surgery Adult Aged Carcinoma/enzymology,surgery DNA Polymerase II/metabolism Female Graves Disease/enzymology Humans Kinetics Male Middle Aged Thyroid Gland/enzymology,surgery Thyroid Neoplasms/enzymology,surgery Thyroidectomy
Chemicals
DNA Polymerase II
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Nagasaka A
Department of Internal Medicine and Surgery, Fujita-Gakuen Health University School of Medicine, Aichi, Japan.
Yoshida S
Nakai A
Ohyama T
Iwase K
Ohtani S
Shinoda S
Masunaga R
Nakagawa H
Article Info
Journal
Metabolism: clinical and experimental
Abbr.
Metabolism
ISSN
0026-0495
Published
1988-11-00
Pages
1051-4
Language
English
Region
United States
NLM ID
0375267
Subset
IM
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