Anticoagulant drugs increase natural killer cell activity in lung cancer

In preclinical studies in animal models and in initial clinical trials, anticoagulation drugs have been shown to be effective in the prevention and treatment of haematogenous metastasis, and in the prolongation of survival in animal models. However, only a few studies have been performed on the dire...

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Published inLung cancer (Amsterdam, Netherlands) Vol. 47; no. 2; pp. 215 - 223
Main Authors Bobek, V., Boubelik, M., Fišerová, A., L’uptovcová, M., Vannucci, L., Kacprzak, G., Kolodzej, J., Majewski, A.M., Hoffman, R.M.
Format Journal Article
LanguageEnglish
Published Shannon Elsevier Ireland Ltd 01.02.2005
Elsevier Science
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Online AccessGet full text
ISSN0169-5002
1872-8332
DOI10.1016/j.lungcan.2004.06.012

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Abstract In preclinical studies in animal models and in initial clinical trials, anticoagulation drugs have been shown to be effective in the prevention and treatment of haematogenous metastasis, and in the prolongation of survival in animal models. However, only a few studies have been performed on the direct influence of anticoagulation drugs on the immune system. The purpose of this study is to determine the effect of warfarin, unfractioned heparin, low molecular weight heparins (LMWHs), and acetylsalicylic acid anticoagulants on the functional activity of natural killer (NK) cells. Cytotoxic activity in patients with early, operable stages of non-small-cell lung cancer was compared with healthy volunteers. Cytotoxic studies were also carried out in tumor-bearing animals. Lung-cancer patients were characterized by significantly lower NK cell cytotoxicity (7.07 ± 3.15) than healthy donors (44.12 ± 10.62, P < 0.001). NK cell activation was found in both in vitro experiments using peripheral blood mononuclear cells (PBMC) from healthy donors and ex vivo in lung carcinoma patients after treatment with unfractionated heparin and fraxiparine. Similarly, potentiation of NK cell activity in Lewis lung carcinoma-bearing mice was found after therapy with unfractionated heparin. NK cell activity is lower in lung cancer patients than in normal subjects. NK cell activation was increased by LMWHs. Other anticoagulants augment the effector function of NK cells in cancer patients and in an animal model of lung cancer. This is a novel effect of these compounds, which were thought previously to exert their effect only via their anticoagulant properties.
AbstractList In preclinical studies in animal models and in initial clinical trials, anticoagulation drugs have been shown to be effective in the prevention and treatment of haematogenous metastasis, and in the prolongation of survival in animal models. However, only a few studies have been performed on the direct influence of anticoagulation drugs on the immune system. The purpose of this study is to determine the effect of warfarin, unfractioned heparin, low molecular weight heparins (LMWHs), and acetylsalicylic acid anticoagulants on the functional activity of natural killer (NK) cells. Cytotoxic activity in patients with early, operable stages of non-small-cell lung cancer was compared with healthy volunteers. Cytotoxic studies were also carried out in tumor-bearing animals. Lung-cancer patients were characterized by significantly lower NK cell cytotoxicity (7.07 +/- 3.15) than healthy donors (44.12 +/- 10.62, P < 0.001). NK cell activation was found in both in vitro experiments using peripheral blood mononuclear cells (PBMC) from healthy donors and ex vivo in lung carcinoma patients after treatment with unfractionated heparin and fraxiparine. Similarly, potentiation of NK cell activity in Lewis lung carcinoma-bearing mice was found after therapy with unfractionated heparin. NK cell activity is lower in lung cancer patients than in normal subjects. NK cell activation was increased by LMWHs. Other anticoagulants augment the effector function of NK cells in cancer patients and in an animal model of lung cancer. This is a novel effect of these compounds, which were thought previously to exert their effect only via their anticoagulant properties.
In preclinical studies in animal models and in initial clinical trials, anticoagulation drugs have been shown to be effective in the prevention and treatment of haematogenous metastasis, and in the prolongation of survival in animal models. However, only a few studies have been performed on the direct influence of anticoagulation drugs on the immune system. The purpose of this study is to determine the effect of warfarin, unfractioned heparin, low molecular weight heparins (LMWHs), and acetylsalicylic acid anticoagulants on the functional activity of natural killer (NK) cells. Cytotoxic activity in patients with early, operable stages of non-small-cell lung cancer was compared with healthy volunteers. Cytotoxic studies were also carried out in tumor-bearing animals. Lung-cancer patients were characterized by significantly lower NK cell cytotoxicity (7.07 ± 3.15) than healthy donors (44.12 ± 10.62, P < 0.001). NK cell activation was found in both in vitro experiments using peripheral blood mononuclear cells (PBMC) from healthy donors and ex vivo in lung carcinoma patients after treatment with unfractionated heparin and fraxiparine. Similarly, potentiation of NK cell activity in Lewis lung carcinoma-bearing mice was found after therapy with unfractionated heparin. NK cell activity is lower in lung cancer patients than in normal subjects. NK cell activation was increased by LMWHs. Other anticoagulants augment the effector function of NK cells in cancer patients and in an animal model of lung cancer. This is a novel effect of these compounds, which were thought previously to exert their effect only via their anticoagulant properties.
In preclinical studies in animal models and in initial clinical trials, anticoagulation drugs have been shown to be effective in the prevention and treatment of haematogenous metastasis, and in the prolongation of survival in animal models. However, only a few studies have been performed on the direct influence of anticoagulation drugs on the immune system.BACKGROUNDIn preclinical studies in animal models and in initial clinical trials, anticoagulation drugs have been shown to be effective in the prevention and treatment of haematogenous metastasis, and in the prolongation of survival in animal models. However, only a few studies have been performed on the direct influence of anticoagulation drugs on the immune system.The purpose of this study is to determine the effect of warfarin, unfractioned heparin, low molecular weight heparins (LMWHs), and acetylsalicylic acid anticoagulants on the functional activity of natural killer (NK) cells.OBJECTIVEThe purpose of this study is to determine the effect of warfarin, unfractioned heparin, low molecular weight heparins (LMWHs), and acetylsalicylic acid anticoagulants on the functional activity of natural killer (NK) cells.Cytotoxic activity in patients with early, operable stages of non-small-cell lung cancer was compared with healthy volunteers. Cytotoxic studies were also carried out in tumor-bearing animals.PATIENTS AND METHODCytotoxic activity in patients with early, operable stages of non-small-cell lung cancer was compared with healthy volunteers. Cytotoxic studies were also carried out in tumor-bearing animals.Lung-cancer patients were characterized by significantly lower NK cell cytotoxicity (7.07 +/- 3.15) than healthy donors (44.12 +/- 10.62, P < 0.001). NK cell activation was found in both in vitro experiments using peripheral blood mononuclear cells (PBMC) from healthy donors and ex vivo in lung carcinoma patients after treatment with unfractionated heparin and fraxiparine. Similarly, potentiation of NK cell activity in Lewis lung carcinoma-bearing mice was found after therapy with unfractionated heparin. NK cell activity is lower in lung cancer patients than in normal subjects.RESULTSLung-cancer patients were characterized by significantly lower NK cell cytotoxicity (7.07 +/- 3.15) than healthy donors (44.12 +/- 10.62, P < 0.001). NK cell activation was found in both in vitro experiments using peripheral blood mononuclear cells (PBMC) from healthy donors and ex vivo in lung carcinoma patients after treatment with unfractionated heparin and fraxiparine. Similarly, potentiation of NK cell activity in Lewis lung carcinoma-bearing mice was found after therapy with unfractionated heparin. NK cell activity is lower in lung cancer patients than in normal subjects.NK cell activation was increased by LMWHs. Other anticoagulants augment the effector function of NK cells in cancer patients and in an animal model of lung cancer. This is a novel effect of these compounds, which were thought previously to exert their effect only via their anticoagulant properties.CONCLUSIONSNK cell activation was increased by LMWHs. Other anticoagulants augment the effector function of NK cells in cancer patients and in an animal model of lung cancer. This is a novel effect of these compounds, which were thought previously to exert their effect only via their anticoagulant properties.
Author Fišerová, A.
Majewski, A.M.
Kolodzej, J.
L’uptovcová, M.
Kacprzak, G.
Hoffman, R.M.
Bobek, V.
Vannucci, L.
Boubelik, M.
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  surname: Kolodzej
  fullname: Kolodzej, J.
  organization: Department of Thoracic Surgery of Medical Academy, Lower Silesian Centre of Lung Diseases, Grabiszynska 105, 53-439 Wroclaw, Poland
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  surname: Majewski
  fullname: Majewski, A.M.
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  surname: Hoffman
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  organization: AntiCancer, Inc., 7917 Ostrow Street, San Diego, CA 92111, USA
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Issue 2
Keywords Natural killer cell
Anticoagulants
LMWHs
Warfarin
Lewis lung cancer
Heparin
NK activity
Cancer
Drug
Lung disease
Respiratory disease
Lung cancer
Activity
Anticoagulant
Increase
Malignant tumor
Natural
Natural iller cell
Blood group
Bronchus disease
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Snippet In preclinical studies in animal models and in initial clinical trials, anticoagulation drugs have been shown to be effective in the prevention and treatment...
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SubjectTerms Aged
Animals
Anticoagulants
Anticoagulants - pharmacology
Anticoagulants - therapeutic use
Biological and medical sciences
Cancer
Carcinoma, Lewis Lung - immunology
Carcinoma, Non-Small-Cell Lung - immunology
Case-Control Studies
Female
Heparin
Humans
Killer Cells, Natural - immunology
Lewis lung cancer
LMWHs
Lung Neoplasms - immunology
Male
Medical sciences
Mice
Middle Aged
Natural killer cell
NK activity
Pneumology
Tumor Cells, Cultured
Tumors of the respiratory system and mediastinum
Warfarin
Title Anticoagulant drugs increase natural killer cell activity in lung cancer
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0169500204003101
https://dx.doi.org/10.1016/j.lungcan.2004.06.012
https://www.ncbi.nlm.nih.gov/pubmed/15639720
https://www.proquest.com/docview/67355649
Volume 47
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