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Featured researches published by Junjiro Sano.


Japanese Journal of Cancer Research | 1988

Pepsinogens I and II in Gastric Cancer: An Immunohistochemical Study Using Monoclonal Antibodies

Shih-Che Huang; Kazumasa Miki; Junjiro Sano; Masao Ichinose; Norio Kawamura; Hiroshi Oka; Kazuyuki Hirano; Chie Furihata; Yozo Masugi; Kenji Takahashi

Monoclonal antibodies were used to examine the immunohistochemical expression of pepsinogens I and II in 31 early and 76 advanced gastric cancers. Of the 107 carcinomas studied, 19 contained pepsinogen II and only 3, found exclusively in pepsinogen II‐positive cases, contained pepsinogen I. Gastric cancer produces pepsinogen II more frequently than pepsinogen I, and production of the latter is significantly associated with the former. Historically, there were 54 intestinal‐type and 53 diffuse‐type cancers. The former produced pepsinogen II more frequently than the latter. In the diffuse type, the four pepsinogen II‐positive cases were found exclusively in females. Although the pepsinogen expression was independent of the macroscopic features in advanced gastric cancer, it was found that the protruded‐type early gastric cancer produced pepsinogen II more frequently than the depressed type. Incidences of pepsinogen positivity were not different between early and advanced gastric cancers or between cancers with or without lymph node metastasis, suggesting that production of pepsinogen is independent of tumor growth.


Pathology International | 1989

In Situ Localization of Pepsinogens I and II mRNA in Human Gastric Mucosa

Junjiro Sano; Kazumasa Miki; Masao Ichinose; Masayoshi Kimura; Kiyoshi Kurokawa; Takeo Aida; Masamichi Ishizaki; Goro Asano; Yozo Masugi; Ricky N.S. Wong; Kenji Takahashi

Localization of pepsinogens I and II mRNA in the human gastric mucosa was investigated by an in situ hybridization method using digoxigenin labeled cDNA probes. Gastric fundic mucosa from healthy volunteers, which was stained with digoxigenin labeled pepsinogens I and II cDNA probes, showed positive staining in the cytoplasm of both chief cells and mucous neck cells. In contrast, gastric antral mucosa stained with the pepsinogen I cDNA probe showed no positive reaction in the surface mucous cells or pyloric glands. On the other hand, the pyloric glands were stained positively with the pepsinogen II cDNA probe and the staining appeared to be identical to that obtained with the anti pepsinogens I and II monoclonal antibodies using the avidin biotin peroxidase complex technique. These results are consistent with those of previous studies that have employed immunochemical and immunohistochemical techniques. Acta Pathol Jpn 39: 765 771, 1989.


Japanese Journal of Cancer Research | 1991

Methylation and Expression of Human Pepsinogen Genes in Normal Tissues and Their Alteration in Stomach Cancer

Masao Ichinose; Kazumasa Miki; Ricky N. S. Wong; Masae Tatematsu; Chie Furihata; Toshiro Konishi; Masashi Matsushima; Masao Tanji; Junjiro Sano; Kiyoshi Kurokawa; Takayuki Takahashi; Takashi Kageyama; Jordan J. N. Tang; Kenji Takahashi

In normal human tissues, pepsinogen A mRNA was expressed only in the fundic mucosa of the stomach, whereas pepsinogen C mRNA was expressed in all regions of the stomach mucosa and also in the proximal duodenal mucosa. The distributions of these mRNAs were consistent with those of pepsinogens A and C in the gastroduodenal mucosa. Methylation analysis of DNAs from normal tissues with methylation‐sensitive restriction enzymes, Hpa II and Hha I, revealed that pepsinogen A and C genes are hypomethylated in tissues producing pepsinogens A and C, suggesting a role of DNA methylation in the regulation of the differential expression of the genes for the two human pepsinogens during normal differentiation. In stomach cancer tissues and cancer cell lines, the expressions of the pepsinogen genes were decreased or lost, in good accordance with their pepsinogen productions. No gross structural changes of the pepsinogen genes were observed in these cancers, but the methylation patterns of the pepsinogen genes were found to be altered in different ways in different cancers. The functional significance of the altered methylation is unknown; however, these results suggest that considerable heterogeneity of the methylation patterns occurs in human stomach cancers.


Journal of Clinical Gastroenterology | 1995

Lansoprazole for maintenance therapy of peptic ulcer disease: weekend full-dose or everyday half-dose administration?

Etsuo Hoshino; Noritsugu Umeda; Junjiro Sano; Kazumasa Miki; Naohisa Yahagi; Masashi Oka; Masayoshi Kimura; Hideo Miyashita

Seventy-one patients with peptic ulcer (44 gastric ulcer and 27 duodenal ulcer patients) were enrolled in this study. After the ulcers had healed with 2 months of treatment with lansoprazole (LPZ) 30 mg/day, patients were divided into two groups: 43 in the half-dose q.d. group and 28 in the weekend full-dose group. Fourteen (23%) of the 43 patients in the half-dose q.d. group and 14 of the 28 (50%) in the weekend full-dose group failed to continue taking the drug for 6 months owing to poor compliance (p < 0.05). None of the 30 patients who continued to take the maintenance dose of LPZ experienced ulcer recurrence during the 6-month follow-up period, whereas 71% of the patients who stopped taking LPZ experienced recurrence (p < 0.01). In conclusion, maintenance therapy using the half-dose q.d. administration schedule was superior to weekend full-dose administration because of the better patient compliance and a lower ulcer recurrence rate.


Digestive Endoscopy | 1990

A Case of Extensive Gastrointestinal Involvement of Malignant Lymphoma Associated with Early Gastric Carcinoma

Nobuyuki Kakei; Kazumasa Miki; Masayoshi Kimura; Junjiro Sano; Masao Ichinose; Etsuo Hoshino; Norio Kawamura; Takao Tashiro; Masashi Matsushima; Kiyoshi Kurokawa

Abstract: Described is a 59 year old Japanese man With malignant lymphoma involving the stomach, duodenum, terminal ileum, colon and rectum, who developed early gastric carcinoma. Repeated gastroduodenoscopy revealed various appearances of the gastrointestinal involvement in malignant lymphoma, such as giant folds, polypoid lesions, and ulcerations, in addition to a depressed lesion of early gastric carcinoma. Colonoscopy also showed multiple polypoid lesions throughout the large bowel. Though the gastrointestinal involvement in malignant lymphoma is not rare, diffuse multiple polypoid lesions in the entire large bowel as seen in our case have rarely been endoscopically described.


Digestive Endoscopy | 1989

Ascending Colon Stenosis:A Rare Presentation of Perforated Appendicitis

Nobuyuki Kakei; Kazumasa Miki; Masayoshi Kimura; Masao Ichinose; Etsuo Hoshino; Junjiro Sano; Norio Kawamura; Takao Tashiro; Masashi Matsushima; Kiyoshi Kurokawa; Daijo Hashimoto; Yasuo Idezuki

Abstract: Described is a 49‐year‐old Japanese male who developed an ascending colon stenosis secondary to perforated appendicitis. The patient was examined at our hospital because of an abdominal pain and the presence of a firm mass in the right flank. A barium enema and colonoscopic examination revealed an ascending colon stenosis with multiple nodular elevations. On laparotomy, an inflammatory mass, originating from a ruptured appendix, was found adhered to the cecum and the ascending colon. Thus, a right hemicolectomy was performed. Microscopic examination revealed a periappendiceal abscess with marked submucosal fibrosis and lymphoid hyperplasia of the ascending colon and cecum.


Japanese Journal of Cancer Research | 1989

The Significance of Low Serum Pepsinogen Levels to Detect Stomach Cancer Associated with Extensive Chronic Gastritis in Japanese Subjects

Kazumasa Miki; Masao Ichinose; Norio Kawamura; Masashi Matsushima; Haron Bin Ahmad; Masayoshi Kimura; Junjiro Sano; Takao Tashiro; Nobuyuki Kakei; Hiroshi Oka; Chie Furihata; Kenji Takahashi


Journal of Cellular Physiology | 1985

Activation of collagen synthesis in primary culture of rat liver parenchymal cells (hepatocytes)

Ryu-Ichiro Hata; Yoshifumi Ninomiya; Junjiro Sano; Hiroshi Konomi; Hisae Hori; Hironobu Sunada; Shizuko Tanaka; Keiichiro Kabuki; Yutaka Nagai; Yutaka Tsukada


Biomedical Research-tokyo | 1980

The presence of Thy-1.1 antigen in rat glomerular mesangial cells.

Masamichi Ishizaki; Shigeru Sato; Junjiro Sano; Yuh Fukuda; Yuhichi Sugisaka; Yozo Masugi


Biomedical Research-tokyo | 1981

IMMUNOHISTOCHEMICAL LOCALIZATION OF TYPES I, III AND IV (BASEMENT MEMBRANE) COLLAGENS IN THE LYMPH NODE: CO-DISTRIBUTION OF TYPES I AND III COLLAGENS IN THE RETICULAR FIBERS

Hiroshi Konomi; Junjiro Sano; Yutaka Nagai

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Masao Ichinose

Wakayama Medical University

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Hiroshi Konomi

Tokyo Medical and Dental University

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Kiyoshi Kurokawa

National Graduate Institute for Policy Studies

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