Yuka Miyasaka
Tokyo Medical and Dental University
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Yuka Miyasaka.
Journal of Gastroenterology and Hepatology | 2001
Junichi Tazawa; Manabu Maeda; Yoshinori Sakai; Michio Yamane; Hideo Ohbayashi; Sei Kakinuma; Yuka Miyasaka; Kazuyoshi Nagayama; Nobuyuki Enomoto; Chifumi Sato
The aim of this study was to examine the effectiveness and toxicity of radiation therapy in combination with transcatheter arterial chemoembolization (TACE) for hepatocellular carcinoma (HCC) with extensive portal vein tumor thrombus (PVTT).
British Journal of Cancer | 2001
Yuka Miyasaka; Nobuyuki Enomoto; Kazuyoshi Nagayama; Namiki Izumi; Fumiaki Marumo; Mamoru Watanabe; Chifumi Sato
The genetic basis of hepatocellular carcinoma (HCC) has not yet been fully understood. Although various methods have been developed to detect differentially expressed genes in malignant diseases, efficient analysis from clinical specimens is generally difficult to perform due to the requirement of a large amount of samples. In the present study, we analysed differentially expressed genes with a small amount of human HCC samples using suppression subtractive hybridization (SSH). Total RNA were obtained from the hepatitis C virus-associated HCC and adjacent non-HCC liver tissues. cDNA was synthesized using modified RT-PCR, and then tester cDNA was ligated with 2 different kinds of adaptors and hybridized with an excess amount of driver cDNA. Tester specific cDNA was obtained by suppression PCR and the final PCR product was subcloned and sequenced. We identified 7 known genes (focal adhesion kinase, deleted in colon cancer, guanine binding inhibitory protein α, glutamine synthetase, ornithine aminotransferase, M130, and pepsinogen C) and 2 previously unknown genes as being overexpressed in HCC, and 1 gene (decorin) as suppressed in HCC. Quantitative analysis of gene expression using quantitative RT-PCR demonstrated the differential expression of these genes in the original and other HCC samples. These findings demonstrated that it is possible to identify the previously unknown, differential gene expression from a small amount of clinical samples. Information about such alterations in gene expression could be useful for elucidating the genetic events in HCC pathogenesis, developing the new diagnosic markers, or determining novel therapeutic targets.
The American Journal of Gastroenterology | 1999
Kazuyoshi Nagayama; Junichi Tazawa; Yoshinori Sakai; Yuka Miyasaka; Shin-Han Yu; Ikuo Sakuma; Shinya Maekawa; Hideo Obayashi; Fumaiaki Marumo; Chifumi Sato
Objective:Although endoscopic clipping is used widely for the treatment of bleeding gastroduodenal ulcers, clinical trials on its efficacy are scarce. The aim of this study is to assess the efficacy and safety of endoscopic clipping for hemostasis from bleeding gastroduodenal ulcers.Methods:The present study was designed as a retrospective study using historical controls. One hundred consecutive patients with bleeding gastroduodenal ulcers were treated by endoscopic clipping. The preceding 91 consecutive patients treated by endoscopic pure ethanol injection were regarded as controls. Forty-nine of the clipping group and 41 of the ethanol group had lesions at sites difficult to perform endoscopic manipulation. Hemostatic rates, rebleeding rates, amounts of blood transfusion, and durations of hospital stay were analyzed.Results:The hemostatic rate was 96% in both clipping and ethanol groups, whereas the rebleeding rate was lower (15%vs 29%, p= 0.023) in the former than the latter. In technically difficult cases, the hemostatic rate was comparable (96 vs 90%).Conclusion:In patients with bleeding gastroduodenal ulcers, endoscopic clipping may be a choice of therapy because of a low rebleeding rate compared with pure ethanol injection.
The Journal of Infectious Diseases | 2003
Yuka Miyasaka; Nobuyuki Enomoto; Masayuki Kurosaki; Naoya Sakamoto; Nobuhiko Kanazawa; Takahiro Kohashi; Eri Ueda; Shinya Maekawa; Hideki Watanabe; Namiki Izumi; Chifumi Sato; Mamoru Watanabe
To analyze the influence of hepatitis C virus nonstructural protein 5A (NS5A) on apoptosis, we established Huh7 cells that stably express NS5A, and induced apoptosis using tumor necrosis factor (TNF)-alpha. The viability of control Huh7 cells was reduced to 40%, compared with untreated cells, after TNF-alpha treatment, whereas that of Huh7-NS5A cells was reduced only to 80%. DNA fragmentation also decreased to <50% in Huh7-NS5A compared with control cells. Nuclear factor-kappaB activation was the same in both cell types, whereas caspase-8, -9, and -3 activity was decreased in Huh7-NS5A cells, compared with control cells, which indicates that the inhibition of caspase-8 activation is responsible for the antiapoptotic effect of the NS5A protein. The coexpression of NS5A did not inhibit apoptosis induced by caspase-8 or Fas-associating death domain protein expression. These findings suggest that the NS5A protein inhibits the apoptotic effect of TNF-alpha upstream of caspase-8 in the apoptosis cascade.
The American Journal of Gastroenterology | 2001
Kazuyoshi Nagayama; Nobuyuki Enomoto; Yuka Miyasaka; Masayuki Kurosaki; Cheng-Hsin Chen; Naoya Sakamoto; Mina Nakagawa; Chifumi Sato; Junichi Tazawa; Takaaki Ikeda; Namiki Izumi; Mamoru Watanabe
OBJECTIVE:To clarify gene expression profiles in the liver may elucidate the pathogenesis of type I autoimmune hepatitis (AIH). Using suppression subtractive hybridization (SSH), we identified genes overexpressed in the liver of AIH.METHODS:A small liver biopsy sample from a patient with definite AIH was available to be analyzed in our system. By mixing cDNA synthesized from this sample as a ‘tester’ and cDNA from a normal liver as a ‘driver,’ we subtracted cDNA to enrich genes overexpressed in AIH. After polymerase chain reaction (PCR) amplification and subcloning, we identified subtracted genes by sequencing 50 randomly selected clones.RESULTS:Only one cDNA fragment, which is identical to interferon inducible protein 10 (IP-10), was overexpressed by >10 times in the liver of AIH, as compared with control. We confirmed IP-10 overexpression in all eight patients with AIH by reverse transcription PCR. Immunohistochemical analysis demonstrated increased IP-10 expression in hepatocytes in the liver of AIH. Reverse transcription PCR analysis of 63 liver biopsy samples with various liver diseases revealed that IP-10 expression was significantly higher in AIH (p = 0.025) and chronic hepatitis C (p = 0.0043) than in other liver diseases. Interestingly, the amount of IP-10 mRNA expression was correlated with serum ALT values in AIH (p = 0.0006), but not in chronic hepatitis C (p = 0.43).CONCLUSION:These results indicate the IP-10 expression in the liver might be used as a preferential marker of AIH, and that IP-10 has some pathophysiological roles in the liver damage of AIH.
British Journal of Cancer | 2004
H Takenawa; Masayuki Kurosaki; Nobuyuki Enomoto; Yuka Miyasaka; Nobuhiko Kanazawa; Naoya Sakamoto; Takaaki Ikeda; Namiki Izumi; Chifumi Sato; Mamoru Watanabe
Gastric adenomas may eventually progress to adenocarcinomas at varying rates. The purpose of the present study was to identify gene-expression profiles linked to the heterogeneous nature of gastric adenoma as compared to adenocarcinoma. Suppression subtractive hybridisation analysis was performed to extract relevant genes from two cases of low- and high-grade gastric adenomas. The identified genes were quantified by RT–PCR in 14 low-grade adenoma, nine high-grade adenoma and nine adenocarcinoma samples, followed by hierarchical clustering analysis to separate tumours into groups according to their gene-expression profiles. Nine genes previously implicated in carcinogenesis in a variety of organs, including three genes related to gastric adenocarcinoma, were identified. The overexpression of these genes in gastric adenoma has not been reported previously. The clustering analysis of these nine genes across 32 cases identified three groups, one of which consisted primarily of adenocarcinomas, whereas the other two groups consisted of adenomas. One group of adenomas, characterised by larger tumour size, exhibited gene-expression profiles of an intestinal cell lineage implicated in the pathogenesis of an intestinal-type gastric adenocarcinoma. Another adenoma group consisting of low-grade adenomas with smaller tumour size exhibited a unique expression profile. In conclusion, clustering analysis of expression profiles using a limited number of genes may serve as molecular markers for gastric adenoma with different biological properties. Although the prognostic values of these gene-expression profiles need to be evaluated in further follow-up study of adenoma cases, these findings add new insights to (a) our understanding of the pathogenesis of gastric tumours, (b) the development of specific tumour markers for clinical practice, and (c) the design of novel therapeutic targets.
Journal of Clinical Gastroenterology | 2000
Junichi Tazawa; Yoshinori Sakai; Michio Yamane; Sei Kakinuma; Manabu Maeda; Keiko Suzuki; Yuka Miyasaka; Kazuyoshi Nagayama; Fumihiko Kusano; Chifumi Sato
Two patients with hepatocellular carcinoma (HCC) were treated with transjugular intrahepatic portosystemic stent-shunt (TIPS) and followed for 22 and 58 months thereafter. HCC was well controlled by transcatheter arterial chemoembolization. Hepatic failure or metastasis, especially in the lung, was not observed in the long-term observation. TIPS seems to be useful even in patients with HCC, provided HCC is controlled.
Hepatology | 2000
Kazuyoshi Nagayama; Masayuki Kurosaki; Nobuyuki Enomoto; Yuka Miyasaka; Fumiaki Marumo; Chifumi Sato
Virology | 1999
Kazuyoshi Nagayama; Masayuki Kurosaki; Nobuyuki Enomoto; Shinya Maekawa; Yuka Miyasaka; Junichi Tazawa; Namiki Izumi; Fumiaki Marumo; Chifumi Sato
Internal Medicine | 1997
Kazuyoshi Nagayama; Namiki Izumi; Yuka Miyasaka; Kazunori Saito; Keiichi Ono; Osamu Noguchi; Yuji Hoshino; Masakatsu Uchihara; Shozo Miyake; Nobuyuki Enomoto; Yujiro Tanaka; Fumiaki Marumo; Chifumi Sato