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Dive into the research topics where Kayoko Shimizu is active.

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Featured researches published by Kayoko Shimizu.


Clinica Chimica Acta | 1993

Establishment of assay kits for the determination of microheterogeneities of alpha-fetoprotein using lectin-affinity electrophoresis

Kayoko Shimizu; Tomoko Taniichi; Shinji Satomura; Shuji Matsuura; Hiroko Taga; Kazuhisa Taketa

Diagnostic kits for determination of alpha-fetoprotein (AFP) carbohydrate chain microheterogeneity were developed using lectin affinity electrophoresis with Lens culinaris agglutinin-A (LCA-A) and erythro-agglutinating phytohemagglutinin-E4 (PHA-E4). Separated AFP bands by electrophoresis were detected with high sensitivity by antibody-affinity blotting and immunoenzymatic amplification. Densitometry was used to apportion lectin reactive AFPs. The within-run S.D. for proportions of AFP bands was below 3%. Band intensity was linearly related to AFP concentration between 2 and 200 ng/ml. Profiles of lectin reactive AFPs were compared in serum samples from 55 patients having liver diseases. The average values of lectin reactive AFPs for chronic hepatitis and liver cirrhosis patients were both below 13%, but those of hepatocellular carcinoma patients were above 25%. Correlation of data with disease states suggests that the methods can greatly facilitate the discrimination between benign and malignant liver diseases.


Clinica Chimica Acta | 1996

Comparison of carbohydrate structures of serum α-fetoprotein by sequential glycosidase digestion and lectin affinity electrophoresis

Kayoko Shimizu; Hideo Katoh; Fumihiko Yamashita; Masatoshi Tanaka; Kyuichi Tanikawa; Kazuhisa Taketa; Shinji Satomura; Shuji Matsuura

Serum alpha-fetoprotein (AFP) is a glycoprotein of which the sugar chain is considered to show structural changes with malignancies. Microheterogeneity of the serum AFP carbohydrate structure was studied in samples from 35 patients with benign and malignant diseases. Sera were digested directly, extensively, and sequentially with sialidase. beta-galactosidase and beta-N-acetylhexosaminidase. Before and after digestion, sera were examined by means of lectin affinity electrophoresis using eight lectins. Relationships between AFP carbohydrate structures and liver diseases were elucidated by the lectin-reactive profiles and the effect of glycosidase digestion. More than 94% of the AFP carbohydrate structures found in patients with benign and malignant liver diseases were biantennary complex-type oligosaccharides. Changes in the AFP carbohydrate structures at the early stage of hepatocellular carcinoma revealed the addition of alpha 1-->6 fucose to the reducing terminal N-acetylglucosamine and monosialylated AFPs. In both advanced hepatocellular carcinoma and AFP producing extrahepatic malignancies, AFP carbohydrate structures were characterized as the further addition of beta 1-->4 N-acetylglucosamine and heterogeneity in the galactose and N-acetylglucosamine residues. Sequential glycosidase digestion and lectin affinity electrophoresis is useful for analysing the carbohydrate structures of serum glycoprotein.


Clinica Chimica Acta | 2001

Alpha-fetoprotein microheterogeneity: a potential biochemical marker for Down’s syndrome

Ritsu Yamamoto; Masaki Azuma; Yukio Wakui; Tatsuro Kishida; Hideto Yamada; Kazuhiko Okuyama; Tadashi Sagawa; Kayoko Shimizu; Shinji Satomura; Seiichiro Fujimoto

Our purpose was to examine the utility of analyzing alpha-fetoprotein (AFP) microheterogeneity assessed by lectin affinity in Downs syndrome (DS) screening. Maternal sera and amniotic fluids were collected from 18 women who were carrying DS fetuses and 70 unaffected pregnancies around 16 weeks of gestation. The percentages of AFP which reacted with Lens culinaris agglutinin (AFP-L2,3) were determined by lectin affinity electrophoresis. AFP-L2,3 levels were significantly increased (P<0.0001) in both maternal serum and amniotic fluid from DS-affected versus unaffected pregnancies. The fractional areas under the receiver operating characteristic curves were 0.835 and 0.700 (P=0.106) for AFP-L3 and AFP MoM (multiples of the median) in maternal serum. No correlation was found between AFP-L3 and AFP MoM in maternal serum (r=0.006). Our data suggest that the measurement of AFP-L3 in maternal serum is a potential biochemical marker for DS.


Clinical Chemistry and Laboratory Medicine | 2009

Evaluation of a new method for the diagnosis of alterations of Lens culinaris agglutinin binding of thyroglobulin molecules in thyroid carcinoma

Toshiharu Kanai; Masao Amakawa; Ryoji Kato; Kayoko Shimizu; Kenji Nakamura; Ken-ichi Ito; Yoshihisa Hama; Minoru Fujimori; Jun Amano

Abstract Background: The measurement of serum thyroglobulin (Tg) is widely used as a marker for recurrence of thyroid carcinoma following total thyroidectomy. However, this method cannot differentiate between benign and malignant disease. We focused on the sugar chain in the Tg molecule and investigated the usefulness of Lens culinaris agglutinin (LCA)-reactive Tg ratios in sera and wash fluids obtained during fine-needle aspiration (FNA) for the detection of thyroid carcinoma. Methods: The study was performed using 203 serum samples (115 from patients with benign thyroid disease and 88 from patients with thyroid carcinomas) and 176 wash fluid samples (143 benign, 21 malignant, and 12 inconclusive). LCA-reactive Tg ratios were determined using an enzyme-linked immunosorbent assay, and a comparison was made between malignant and benign lesions. Results: In serum, the ratio in patients with malignancy was 79.5±6.0 [mean±standard deviation (SD)], significantly lower than in patients with benign lesions (84.9±3.5). The ratios in wash fluid from malignant lesions (75.8±18.9) were also significantly lower than those from benign lesions (85.6±3.9). Conclusions: These results suggest that this method could distinguish between benign and malignant lesions and may be useful for screening serum and wash samples. Clin Chem Lab Med 2009;47:1285–90.


Acta Obstetricia et Gynecologica Scandinavica | 2003

A study on the microheterogeneity of alpha-fetoproteins produced by yolk sac and germ cell tumors

Ritsu Yamamoto; Toshihiro Ohkouchi; Yukio Wakui; Shinichiro Minobe; Hidemichi Watari; Kayoko Shimizu; Shinji Satomura; Noriaki Sakuragi

Background.  It is generally believed that the lower the grade of differentiation of glycoprotein‐producing cells, the more often modification by bisecting N‐acetylglucosamine (GlcNAc) or fucose (Fuc) at the sugar chain of the glycoprotein or increase in branching of side chains occurs. We examined the characteristics of the alpha‐fetoprotein (AFP) sugar chain stored in amniotic and exocoelomic fluid during 5–9 weeks of gestation and analyzed serum‐derived AFP of patients with germ cell tumors.


Acta Obstetricia et Gynecologica Scandinavica | 2005

A study of oligosaccharide variants of alpha-fetoproteins produced by normal fetuses and fetuses with trisomy 21.

Ritsu Yamamoto; Toshihiro Ohkouchi; Kouichi Tabata; Yasuhiko Ebina; Hidemichi Watari; Masataka Kudo; Kayoko Shimizu; Shinji Satomura; Hisanori Minakami; Noriaki Sakuragi

Background.  The mechanisms of the increase in the percentage of alpha‐fetoproteins (AFPs) that strongly binds to Lens culinaris agglutinin (AFP‐L3) in pregnancies with a trisomy 21 fetus have not been analyzed. To investigate the oligosaccharide variants of AFP produced by normal fetuses and fetuses with trisomy 21, the lectin reactivity of AFP was analyzed.


Clinica Chimica Acta | 2007

The clinical utility of Lens culinaris agglutinin-reactive thyroglobulin ratio in serum for distinguishing benign from malignant conditions of the thyroid

Kayoko Shimizu; Kenji Nakamura; Shinzo Kobatake; Shinji Satomura; Masayuki Maruyama; Fumiko Kameko; Junichi Tajiri; Ryoji Kato


Archive | 1999

METHOD FOR MEASURING THYROGLOBULIN

Ryoji Kato; Masayuki Maruyama; Kenji Nakamura; Kayoko Shimizu; Shinji Satomura


Archive | 1999

Methode zur Messung von Thyroglobulin

Ryoji Kato; Masayuki Maruyama; Kenji Nakamura; Shinji Satomura; Kayoko Shimizu


Archive | 1999

Methode zur Messung von Thyroglobulin Method for measuring thyroglobulin

Ryoji Kato; Masayuki Maruyama; Kenji Nakamura; Shinji Satomura; Kayoko Shimizu

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