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Decline in Peripheral Blood Nkg2d+Cd3+Cd56+ Nkt Cells in Metastatic Colorectal Cancer Patients Publisher Pubmed



Gharagozloo M1 ; Rezaei A1 ; Kalantari H2 ; Bahador A3 ; Hassannejad N4 ; Maracy M5 ; Nouri N6 ; Sedghi M6 ; Ghazanfari H1 ; Bayat B7
Authors
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Authors Affiliations
  1. 1. Department of Immunology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
  2. 2. Department of Gasteroenterology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
  3. 3. Department of microbiology, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Department of Cellular and Molecular Biology, Faculty of Sciences, Science and Research Branch of Islamic Azad University, Tehran, Iran
  5. 5. Department of Biostatistics and Epidemiology, School of Public Health, Isfahan University of Medical Sciences, Isfahan, Iran
  6. 6. Genetic lab, Al-Zhohada hospital, Esfahan University of Medical Sciences, Esfahan, Iran
  7. 7. Department of Microbiology, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran

Source: Bratislava Medical Journal Published:2018


Abstract

OBJECTIVE: Colorectal cancer (CRC) is one of the main causes of cancer deaths in the world. This cancer can be divided into non-metastatic and metastatic CRC stages. CD3+CD56+ NKT cell subsets are a minor T cell subset in peripheral blood and conduct the killing of tumor cells in direct manner. Little is obvious about levels and surface markers of these cells such as NKG2D in different cancers, especially in CRC. METHODS: We included 15 non-metastatic (low-grade), 11 non-metastatic (high-grade), 10 metastatic colorectal cancer patients and 18 healthy controls. The percentages of CD3+CD56+ NKT cells and NKG2D+CD56+ NKT cells from samples were analyzed by flow cytometry in peripheral blood mononuclear cells (PBMCs) of samples. RESULTS: We found that there was a significantly lower number of NKG2D+CD3+CD56+ cells in peripheral blood of patients with metastatic colorectal cancer compared with normal controls (77.53 ± 5.79 % vs 90.74 ± 9.84 %; p < 0.01). CONCLUSION: The fact that frequency of NKG2D+CD56+ NKT cells was significantly lower in patients with metastatic colorectal cancer compared to healthy controls strengthens the hypothesis that NKT cells can play a substantial role in the protection against human colorectal cancer, and this opens up avenues for novel studies about elucidating the other aspects of tumor surveillance in CRC progression and immunotherapy.