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Molecular and Clinical Oncology
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Print ISSN: 2049-9450 Online ISSN: 2049-9469
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July-August 2013 Volume 1 Issue 4

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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.

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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.

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Article

Increased IL‑17 production correlates with immunosuppression involving myeloid-derived suppressor cells and nutritional impairment in patients with various gastrointestinal cancers

  • Authors:
    • Takashi Yazawa
    • Masahiko Shibata
    • Kenji Gonda
    • Takeshi Machida
    • Satoshi Suzuki
    • Akira Kenjo
    • Izumi Nakamura
    • Takao Tsuchiya
    • Yoshihisa Koyama
    • Kenichi Sakurai
    • Tatsuo Shimura
    • Ryouichi Tomita
    • Hitoshi Ohto
    • Mitsukazu Gotoh
    • Seiichi Takenoshita
  • View Affiliations / Copyright

    Affiliations: Department of Organ Regulatory Surgery, Fukushima 960‑1295, Japan, Department of Tumor and Host Bioscience, Fukushima 960‑1295, Japan, Department of Immunology, Fukushima 960‑1295, Japan, Department of Regenerative Surgery, Fukushima 960‑1295, Japan, Department of Surgery, Nihon University School of Medicine, Itabashi, Tokyo 173‑8610, Japan, Department of Surgery, Nippon Dental University, Chiyoda, Tokyo 102-8158, Japan, Department of Blood Transfusion and Transplantation Immunology, Fukushima 960‑1295, Japan
  • Pages: 675-679
    |
    Published online on: May 27, 2013
       https://doi.org/10.3892/mco.2013.134
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Abstract

Although a causal relationship between inflammation and innate immunity of cancer is more widely accepted today, many of the precise cell mechanisms mediating this relationship have not been elucidated. Th17 cells, which produce the proinflammatory cytokine interleukin 17 (IL‑17), have been recognized as one of the key factors in the regulation of inflammatory bowel disease and rheumatoid arthritis. This study demonstrated that, in patients with various types of gastrointestinal cancer, IL‑17 production was correlated with myeloid‑derived suppressor cell (MDSC) levels and with markers for nutritional impairment, immune suppression and chronic inflammation. IL‑17 was significantly higher in patients with various types of gastrointestinal cancer compared to normal volunteers. In addition, IL‑17 levels were significantly correlated with neutrophil counts and the neutrophil̸lymphocyte ratio (NLR) and significantly inversely correlated with cell‑mediated immune response indicators [lymphocyte phytohemagglutinin (PHA)‑blastogenesis and IL‑12 induction] and patient nutritional status (prealbumin levels). Circulating MDSC levels were significantly correlated with IL‑17 production. These results suggest that, in human gastrointestinal cancers, chronic inflammation involving IL‑17 may be an important mechanism contributing to disease progression through enhancement of immune suppression or cachexia. Controlling the activation of Th17 cells may prove to be a valuable strategy for the treatment of gastrointestinal cancer patients.
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Copy and paste a formatted citation
Spandidos Publications style
Yazawa T, Shibata M, Gonda K, Machida T, Suzuki S, Kenjo A, Nakamura I, Tsuchiya T, Koyama Y, Sakurai K, Sakurai K, et al: Increased IL‑17 production correlates with immunosuppression involving myeloid-derived suppressor cells and nutritional impairment in patients with various gastrointestinal cancers. Mol Clin Oncol 1: 675-679, 2013.
APA
Yazawa, T., Shibata, M., Gonda, K., Machida, T., Suzuki, S., Kenjo, A. ... Takenoshita, S. (2013). Increased IL‑17 production correlates with immunosuppression involving myeloid-derived suppressor cells and nutritional impairment in patients with various gastrointestinal cancers. Molecular and Clinical Oncology, 1, 675-679. https://doi.org/10.3892/mco.2013.134
MLA
Yazawa, T., Shibata, M., Gonda, K., Machida, T., Suzuki, S., Kenjo, A., Nakamura, I., Tsuchiya, T., Koyama, Y., Sakurai, K., Shimura, T., Tomita, R., Ohto, H., Gotoh, M., Takenoshita, S."Increased IL‑17 production correlates with immunosuppression involving myeloid-derived suppressor cells and nutritional impairment in patients with various gastrointestinal cancers". Molecular and Clinical Oncology 1.4 (2013): 675-679.
Chicago
Yazawa, T., Shibata, M., Gonda, K., Machida, T., Suzuki, S., Kenjo, A., Nakamura, I., Tsuchiya, T., Koyama, Y., Sakurai, K., Shimura, T., Tomita, R., Ohto, H., Gotoh, M., Takenoshita, S."Increased IL‑17 production correlates with immunosuppression involving myeloid-derived suppressor cells and nutritional impairment in patients with various gastrointestinal cancers". Molecular and Clinical Oncology 1, no. 4 (2013): 675-679. https://doi.org/10.3892/mco.2013.134
Copy and paste a formatted citation
x
Spandidos Publications style
Yazawa T, Shibata M, Gonda K, Machida T, Suzuki S, Kenjo A, Nakamura I, Tsuchiya T, Koyama Y, Sakurai K, Sakurai K, et al: Increased IL‑17 production correlates with immunosuppression involving myeloid-derived suppressor cells and nutritional impairment in patients with various gastrointestinal cancers. Mol Clin Oncol 1: 675-679, 2013.
APA
Yazawa, T., Shibata, M., Gonda, K., Machida, T., Suzuki, S., Kenjo, A. ... Takenoshita, S. (2013). Increased IL‑17 production correlates with immunosuppression involving myeloid-derived suppressor cells and nutritional impairment in patients with various gastrointestinal cancers. Molecular and Clinical Oncology, 1, 675-679. https://doi.org/10.3892/mco.2013.134
MLA
Yazawa, T., Shibata, M., Gonda, K., Machida, T., Suzuki, S., Kenjo, A., Nakamura, I., Tsuchiya, T., Koyama, Y., Sakurai, K., Shimura, T., Tomita, R., Ohto, H., Gotoh, M., Takenoshita, S."Increased IL‑17 production correlates with immunosuppression involving myeloid-derived suppressor cells and nutritional impairment in patients with various gastrointestinal cancers". Molecular and Clinical Oncology 1.4 (2013): 675-679.
Chicago
Yazawa, T., Shibata, M., Gonda, K., Machida, T., Suzuki, S., Kenjo, A., Nakamura, I., Tsuchiya, T., Koyama, Y., Sakurai, K., Shimura, T., Tomita, R., Ohto, H., Gotoh, M., Takenoshita, S."Increased IL‑17 production correlates with immunosuppression involving myeloid-derived suppressor cells and nutritional impairment in patients with various gastrointestinal cancers". Molecular and Clinical Oncology 1, no. 4 (2013): 675-679. https://doi.org/10.3892/mco.2013.134
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