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Featured researches published by Ryuji Nakano.


Annals of Otology, Rhinology, and Laryngology | 1995

Analysis of expression of matrix metalloproteinases-2 and -9 in hypopharyngeal squamous cell carcinoma by in situ hybridization.

Yoshimi Miyajima; Ryuji Nakano; Minoru Morimatsu

The gene expression of two type IV collagenases (matrix metalloproteinase [MMP]-2, a 72 kd type IV collagenase, and MMP-9, a 92 kd type IV collagenase) was investigated in carcinomas of the hypopharynx. We examined 27 cases operated on in our hospital by an in situ hybridization technique to detect their messenger RNA signals in cancer cells and surrounding stroma. Both signals were detected in all cancer nests and in stromal cells in the same specimens. Clinicopathologic studies showed a significant relationship between MMP-2 expression in the primary cancer and the outcome of treatment. Our present study suggests that hypopharyngeal squamous cell carcinoma producing MMP-2 has a high potential for invasion and metastasis and a poor outcome. The analysis of MMPs will be useful for treatment planning in hypopharyngeal carcinoma and for prognosis.


Modern Pathology | 2012

Association of microRNA-21 expression with its targets, PDCD4 and TIMP3, in pancreatic ductal adenocarcinoma.

Yuichi Nagao; Masanori Hisaoka; Atsuji Matsuyama; Shuichi Kanemitsu; Tetsuo Hamada; Tokihiko Fukuyama; Ryuji Nakano; Akihiko Uchiyama; Masahiko Kawamoto; Koji Yamaguchi; Hiroshi Hashimoto

Since the discovery of small non-coding RNAs, the analyses of microRNA (miRNA) expression patterns in human cancer have provided new insights into cancer biology. miRNA-21 has been suggested to be one of the miRNAs that have an important role in the development or biological behavior of a variety of malignancies, including pancreatic cancer. This study was conducted to evaluate the relationship between the expression of miRNA-21 and that of its molecular targets, programmed cell death 4 (PDCD4) and tissue inhibitor of metalloproteinase (TIMP3), in pancreatic ductal adenocarcinoma. The study included 65 pancreatic ductal adenocarcinomas and 5 normal pancreatic tissue specimens for comparison. The miRNA expression profiling of five selected pancreatic ductal adenocarcinomas and five normal pancreatic specimens was performed using a microarray platform, and was evaluated by a hierarchical clustering analysis. The miRNA most highly expressed in pancreatic ductal adenocarcinomas (ie, miRNA-21) was further assessed by quantitative real-time reverse transcription PCR (RT-PCR) assays in the 65 pancreatic ductal adenocarcinoma cases. The expression pattern of its molecular targets (eg, PDCD4 and TIMP3) in pancreatic ductal adenocarcinoma was examined immunohistochemically. In the microarray analyses, 28 miRNAs were upregulated in pancreatic ductal adenocarcinoma compared with normal pancreatic tissue, whereas 48 miRNAs were downregulated. miRNA-21 was the most significantly overexpressed miRNA in the pancreatic ductal adenocarcinomas analyzed, and was also highly expressed in 75% of the 65 pancreatic ductal adenocarcinomas examined by real-time RT-PCR. High miRNA-21 expression was correlated with a worse prognosis in the pancreatic ductal adenocarcinoma patients (P=0.045). The immunohistochemical expression patterns of PDCD4 (reduced nuclear staining pattern) and TIMP3 (downregulated expression) were significantly associated with both the upregulated miR-21 expression (P<0.05) and the poor survival of the patients (P<0.001 and P=0.001, respectively). Our data suggest that an overexpression of miRNA-21 is, therefore, associated with the biological behavior of pancreatic ductal adenocarcinoma via the downregulation of the expression of tumor suppressors, PDCD4 and TIMP3, thus resulting in tumor progression and the adverse clinical course of pancreatic ductal adenocarcinoma.


Fetal and Pediatric Pathology | 1989

Thirty-One Autopsy Cases of Trisomy 18: Clinical Features and Pathological Findings

Masaham Kinoshita; Yasuhiro Nakamura; Ryuji Nakano; Minoru Morimatsu; Seiichi Fukuda; Yasuhiro Nishimi; Takeo Hashimoto

The clinical features and morphological findings in 31 Japanese infants with trisomy 18 are presented. The majority were small-for-date infants. There was no sex predominance in our series, as opposed to male:female ratios of 1:3 reported in the literature. The average age at death was greater in females than in males. Cardiovascular anomalies were consistently present; ventricular septar defect and patent ductus arteriosus being the most common malformations. Various other internal malformations including the Arnold-Chiari malformation were observed.


Virchows Archiv B Cell Pathology Including Molecular Pathology | 1991

Collagenase production by immortalized human aortic endothelial cells infected with simian virus 40

Yasuyuki Sasaguri; Hidetaka Yanagi; Hideaki Nagase; Ryuji Nakano; Shyuichi Fukuda; Minoru Morimatsu

SummaryHuman aortic endothelial cells, isolated at autopsy from a 52-year-old male dying from lung cancer, were treated with simian virus 40 (SV40). One colony was isolated from the infected endothelial cell culture 4 weeks after infection. The cells expressed SV40 large T antigen and p53 protein (p53) in their nuclei but lacted the characteristics of a transformed phenotype. The cells grew well in a monolayer over the 97th passage and exhibited Factor Vlll-related antigen, Ulex europaeus 1 agglutinin (UEA-1) as endothelial cell markers, and a well-developed fibronectin network. The amount of prostacyclin synthesized by the cells was less than the amount synthesized by normal aortic or umbilical cord vein endothelial cells. The cells produced relatively large amounts of procollagenase, and 12-o-tetradecanoyl-phorbol-13-acetate (TPA) augmented the ability of the cells to produce this enzyme. These immortalized human aortic endothelial cells, which have some characteristics of normal endothelial cells and, like capillary endothelial cells, have the ability to produce collagenase, will probably prove useful for studies of atherosclerosis and angiogenesis.


Pathology International | 1984

Anaplastic Giant Cell Tumor With Mucinous Cystadenocarcinoma of The Ovary Origin of the Giant Cells

Kazunari Yamana; Toshihiko Kinoshita; Ryuji Nakano; Minoru Morimatsu; Teruyuki Nakashima

The present case is that of a 27 years old woman who had received right oophorectomy for ovarian cancer nine years previously. The histological diagnosis at that time was mucinous cystadenocarcinoma with anaplastic areas. The patient expired ten years after oophorectomy due to widespread metastases of the tumor. Review of the histological slides revealed ovarian giant cell tumor which was considered to be of epithelial origin differing from those appearing in giant cell tumor of bone.


Pathology International | 1984

Ultrastructure Of Anaplastic Carcinoma (Spindle And Giant Cell Type) With Large Calcification In The Thyroid Gland

Kazunari Yamanay; Ryuji Nakano; Toshihiko Kinoshita; Minoru Morimatsu; Teruyuki Nakashima

Calcification is rare in undifferentiated thyroid carcinoma, because of its rapid progress. We report here such a case seen in a 73‐year‐old male who terminated from pulmonary metastases 4 months after initial diagnosis of spindle and giant cell carcinoma of the thyroid gland. ACTA PATHOL. JPN. 34: 585–592, 1984.


Medical Molecular Morphology | 1995

Ki-1 positive B-cell lymphoma with bizarre giant cells

Yoshimi Miyajima; Ryuji Nakano; Yasuyuki Sasaguri

A 55-year-old woman had complained of swelling on the left side of the neck for 3 weeks. The tumor involved lateral cervical, and inguinal lymph nodes and the faucial tonsil on the left side. The histological diagnosis was Ki-1 positive, non-Hodgkin B-cell lymphoma, with diffuse large cells and bizarre giant cells. Under electron microscopic examination, the tumor cells contained markedly cleaved nuclei, many mitchondria and lamellar rough endoplasmic reticulum. This is the fourth case of Ki-1 positive B-cell lymphoma reported in Japanese literature.


Cardiovascular Pathology | 2017

Calcifying giant cell cardiomyopathy: a possible new entity

Ke-Yong Wang; Sohsuke Yamada; Shohei Shimajiri; Ryuji Nakano; Naoki Yamashita; Tetsuya So; Akihide Tanimoto

We demonstrated an extremely unusual case of an 83-year-old males sudden death secondary to characteristic myocardial necrosis and fibrosis with calcification and multinucleated giant cells infiltration, possibly due to sepsis and Stage IV pulmonary pleomorphic carcinoma-induced cachexia after postmortem study. We propose that this calcifying giant cell cardiomyopathy (CGC) would be a new entity especially from the pathological viewpoints and should be considered in the classification of noninfectious myocarditis. Further prospective studies are needed to validate the presence and significance of CGC and the association with any triggers of somewhat microvascular dysfunction and/or toxic agents, after collecting and investigating a larger number of CGC cases examined.


Journal of Clinical Biochemistry and Nutrition | 1987

Formation of Lipid-Laden Cells from Cultured Aortic Smooth Muscle Cells and Macrophages by Linoleic Acid Hydroperoxide and Low Density Lipoprotein

Kunio Yagi; Taisuke Inagaki; Yasuyuki Sasaguri; Ryuji Nakano; Teruyuki Nakashima


Journal of Surgical Oncology | 1995

Ovarian mucinous cystadenocarcinoma with sarcoma‐like mural nodules

Tetsuo Hamada; Takakazu Sasaguri; Akihide Tanimoto; Nobuyuki Arima; Ryuji Nakano; Yasuyuki Sasaguri; Haruhiko Miyayama

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