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Oncology Reports
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Print ISSN: 1021-335X Online ISSN: 1791-2431
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November 2004 Volume 12 Issue 5

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Journals

International Journal of Molecular Medicine

International Journal of Molecular Medicine

International Journal of Molecular Medicine is an international journal devoted to molecular mechanisms of human disease.

International Journal of Oncology

International Journal of Oncology

International Journal of Oncology is an international journal devoted to oncology research and cancer treatment.

Molecular Medicine Reports

Molecular Medicine Reports

Covers molecular medicine topics such as pharmacology, pathology, genetics, neuroscience, infectious diseases, molecular cardiology, and molecular surgery.

Oncology Reports

Oncology Reports

Oncology Reports is an international journal devoted to fundamental and applied research in Oncology.

Experimental and Therapeutic Medicine

Experimental and Therapeutic Medicine

Experimental and Therapeutic Medicine is an international journal devoted to laboratory and clinical medicine.

Oncology Letters

Oncology Letters

Oncology Letters is an international journal devoted to Experimental and Clinical Oncology.

Biomedical Reports

Biomedical Reports

Explores a wide range of biological and medical fields, including pharmacology, genetics, microbiology, neuroscience, and molecular cardiology.

Molecular and Clinical Oncology

Molecular and Clinical Oncology

International journal addressing all aspects of oncology research, from tumorigenesis and oncogenes to chemotherapy and metastasis.

World Academy of Sciences Journal

World Academy of Sciences Journal

Multidisciplinary open-access journal spanning biochemistry, genetics, neuroscience, environmental health, and synthetic biology.

International Journal of Functional Nutrition

International Journal of Functional Nutrition

Open-access journal combining biochemistry, pharmacology, immunology, and genetics to advance health through functional nutrition.

International Journal of Epigenetics

International Journal of Epigenetics

Publishes open-access research on using epigenetics to advance understanding and treatment of human disease.

Medicine International

Medicine International

An International Open Access Journal Devoted to General Medicine.

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November 2004 Volume 12 Issue 5

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Article

Loss of maspin expression is associated with development and progression of gastric carcinoma with p53 abnormality

  • Authors:
    • Reiko Ito
    • Hirofumi Nakayama
    • Kazuhiro Yoshida
    • Noriko Oda
    • Wataru Yasui
  • View Affiliations / Copyright

    Affiliations: Department of Molecular Pathology, Hiroshima University Graduate School of Biomedical Sciences, Hiroshima University, Minami-ku, Hiroshima 734-8551, Japan
  • Pages: 985-990
    |
    Published online on: November 1, 2004
       https://doi.org/10.3892/or.12.5.985
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Abstract

Maspin, a serine protease inhibitor related to the serpin family, was originally identified in normal mammary epithelium. Reduced expression of maspin is related with development, invasion and metastasis of certain human cancers. In the present study, the expression of maspin was examined in gastric mucosa, adenoma and carcinoma by immunohistochemistry and RT-PCR. In non-neoplastic mucosa, maspin was expressed in cytoplasm and cell membrane of foveolar epithelia, fundic glandular cells and pyloric glandular cells. Maspin expression was lost in 71% (71/100) of gastric carcinomas, and in 19% (4/21) of adenomas, respectively. Loss of maspin expression was significantly associated with poorly differentiated histology, advanced stage and deep invasion (P<0.001). There was an inverse correlation between maspin expression and abnormal p53 accumulation. Maspin mRNA expression was lost in all of 8 gastric carcinoma cell lines that was retrieved after treatment with demethylation agent 5-aza-2'-deoxycytidine in 5 of 8 cell lines. These results suggest that loss of maspin expression partly due to DNA methylation may participate in tumor development and progression of gastric carcinoma in relation with p53 pathway. Loss of maspin expression may serve as a biological marker of high-grade malignancy.

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Copy and paste a formatted citation
Spandidos Publications style
Ito R, Nakayama H, Yoshida K, Oda N and Yasui W: Loss of maspin expression is associated with development and progression of gastric carcinoma with p53 abnormality. Oncol Rep 12: 985-990, 2004.
APA
Ito, R., Nakayama, H., Yoshida, K., Oda, N., & Yasui, W. (2004). Loss of maspin expression is associated with development and progression of gastric carcinoma with p53 abnormality. Oncology Reports, 12, 985-990. https://doi.org/10.3892/or.12.5.985
MLA
Ito, R., Nakayama, H., Yoshida, K., Oda, N., Yasui, W."Loss of maspin expression is associated with development and progression of gastric carcinoma with p53 abnormality". Oncology Reports 12.5 (2004): 985-990.
Chicago
Ito, R., Nakayama, H., Yoshida, K., Oda, N., Yasui, W."Loss of maspin expression is associated with development and progression of gastric carcinoma with p53 abnormality". Oncology Reports 12, no. 5 (2004): 985-990. https://doi.org/10.3892/or.12.5.985
Copy and paste a formatted citation
x
Spandidos Publications style
Ito R, Nakayama H, Yoshida K, Oda N and Yasui W: Loss of maspin expression is associated with development and progression of gastric carcinoma with p53 abnormality. Oncol Rep 12: 985-990, 2004.
APA
Ito, R., Nakayama, H., Yoshida, K., Oda, N., & Yasui, W. (2004). Loss of maspin expression is associated with development and progression of gastric carcinoma with p53 abnormality. Oncology Reports, 12, 985-990. https://doi.org/10.3892/or.12.5.985
MLA
Ito, R., Nakayama, H., Yoshida, K., Oda, N., Yasui, W."Loss of maspin expression is associated with development and progression of gastric carcinoma with p53 abnormality". Oncology Reports 12.5 (2004): 985-990.
Chicago
Ito, R., Nakayama, H., Yoshida, K., Oda, N., Yasui, W."Loss of maspin expression is associated with development and progression of gastric carcinoma with p53 abnormality". Oncology Reports 12, no. 5 (2004): 985-990. https://doi.org/10.3892/or.12.5.985
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