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[Cancer Research 51, 3544-3549, July 1, 1991]
© 1991 American Association for Cancer Research

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Expression of {alpha}-Amylase Isozymes in Human Thyroid Tissues

Sadayuki Doi1, Naohiro Tomita, Masahiko Higasiyama, Hideoki Yokouchi, Akira Horii, Tadashi Yasuda, Tetsuro Kobayashi, Sinichiro Takai, Michio Ogawa, Takesada Mori and Kenichi Matsubara

Institute for Molecular and Cellular Biology, Osaka University, Yamada-oka, Suita, 565 [S. D., N. T., H. Y., A. H., T. Y., K. M.]; Second Department of Surgery, Osaka University Medical School, Fukushima-ku, Osaka 553 [S. D., N. T., M. H., H. Y., A. H., T. Y., T. K., S. T., T. M.]; Second Department of Surgery, Kumamoto University Medical School, Honjyo, Kumamoto 860 [M. O.], Japan

Expression of {alpha}-amylase genes in thyroid tissues was studied by assaying the total amylase activity as well as by using immunohistochemical and Northern blot analysis. The amylase genes expressed were determined by a combination of the polymerase chain reaction (PCR) and blot analysis using synthetic probes specific for the three known amylase isozyme complementary DNAs. The samples consisted of tissues from 18 human thyroid carcinomas (11 well-differentiated carcinomas, 2 poorly differentiated carcinomas, 1 anaplastic carcinoma, and 4 medullary carcinomas) and 9 specimens of nonmalignant thyroid tissue (2 were from nontumorous regions of resected glands and 7 were thyroid tissue from a patient with Graves' disease). Salivary-type amylase was expressed at a relatively high level in nonmalignant thyroid tissue and well-differentiated carcinoma and could be detected by Northern blot analysis. In poorly differentiated carcinoma, it was detected only by the PCR, while in anaplastic or medullary carcinoma, it was not detected even by the PCR. Thus, the expression of salivary-type amylase was characteristic of well-differentiated follicular cells. These observations suggest that salivary-type amylase expression may be a marker for identifying the histogenesis and stage of differentiation of thyroid cancer. In addition, the AMY2B gene product was detected in all different types of cells examined, although its expression was only detectable by the PCR. Pancreatic type amylase was not detected in any of the samples.

1 To whom requests for reprints should be addressed, at Institute for Molecular and Cellular Biology, Osaka University, Yamada-oka, Suita, 565, Japan.

Received 12/17/90. Accepted 4/23/91.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1991 by the American Association for Cancer Research.