Interrelationship between angiogenesis, inflammation and oxidative stress in Indian patients with multiple myeloma
Background Multiple myeloma (MM) is a B-cell malignancy characterized by the accumulation of clonal population of plasma cells in the bone marrow (BM). A variety of angiogenic factors, proteases, reactive oxygen species and inflammatory cytokines induce the formation of an extensive and suitable BM...
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Published in | Clinical & translational oncology Vol. 18; no. 2; pp. 132 - 137 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Milan
Springer Milan
01.02.2016
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Subjects | |
Online Access | Get full text |
ISSN | 1699-048X 1699-3055 |
DOI | 10.1007/s12094-015-1344-5 |
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Abstract | Background
Multiple myeloma (MM) is a B-cell malignancy characterized by the accumulation of clonal population of plasma cells in the bone marrow (BM). A variety of angiogenic factors, proteases, reactive oxygen species and inflammatory cytokines induce the formation of an extensive and suitable BM microenvironment. Previous studies have established the importance of angiogenic factors, inflammatory molecules and oxidative stress in MM but their interplay and effect on each other are not being taken together.
Methods
Circulatory levels of VEGF, angiopoietin-2 (Ang-2), IL-6 and TNF-α along with the activity of superoxide dismutase (SOD) and glutathione peroxidase (GPx) were investigated in 112 subjects including 62 MM patients and 50 healthy controls. Inter-stage analysis was done to evaluate the association of these molecules with the severity of disease. Pearson correlation was determined to find interrelationship, if any, between these molecules.
Results
We have observed elevated levels of VEGF, Ang-2, IL-6, TNF-α and decreased activity of SOD, GPx in MM patients in comparison to controls. All these molecules also showed a trend with the severity of disease. We have found strong association between these factors upon their correlation and regression analysis.
Conclusion
This study is a step toward understanding the indepth contribution of angiogenesis, inflammation and oxidative stress together in making BM microenvironment suitable for growth, survival and proliferation of malignant plasma cells in MM. |
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AbstractList | Background
Multiple myeloma (MM) is a B-cell malignancy characterized by the accumulation of clonal population of plasma cells in the bone marrow (BM). A variety of angiogenic factors, proteases, reactive oxygen species and inflammatory cytokines induce the formation of an extensive and suitable BM microenvironment. Previous studies have established the importance of angiogenic factors, inflammatory molecules and oxidative stress in MM but their interplay and effect on each other are not being taken together.
Methods
Circulatory levels of VEGF, angiopoietin-2 (Ang-2), IL-6 and TNF-α along with the activity of superoxide dismutase (SOD) and glutathione peroxidase (GPx) were investigated in 112 subjects including 62 MM patients and 50 healthy controls. Inter-stage analysis was done to evaluate the association of these molecules with the severity of disease. Pearson correlation was determined to find interrelationship, if any, between these molecules.
Results
We have observed elevated levels of VEGF, Ang-2, IL-6, TNF-α and decreased activity of SOD, GPx in MM patients in comparison to controls. All these molecules also showed a trend with the severity of disease. We have found strong association between these factors upon their correlation and regression analysis.
Conclusion
This study is a step toward understanding the indepth contribution of angiogenesis, inflammation and oxidative stress together in making BM microenvironment suitable for growth, survival and proliferation of malignant plasma cells in MM. Multiple myeloma (MM) is a B-cell malignancy characterized by the accumulation of clonal population of plasma cells in the bone marrow (BM). A variety of angiogenic factors, proteases, reactive oxygen species and inflammatory cytokines induce the formation of an extensive and suitable BM microenvironment. Previous studies have established the importance of angiogenic factors, inflammatory molecules and oxidative stress in MM but their interplay and effect on each other are not being taken together. Circulatory levels of VEGF, angiopoietin-2 (Ang-2), IL-6 and TNF-α along with the activity of superoxide dismutase (SOD) and glutathione peroxidase (GPx) were investigated in 112 subjects including 62 MM patients and 50 healthy controls. Inter-stage analysis was done to evaluate the association of these molecules with the severity of disease. Pearson correlation was determined to find interrelationship, if any, between these molecules. We have observed elevated levels of VEGF, Ang-2, IL-6, TNF-α and decreased activity of SOD, GPx in MM patients in comparison to controls. All these molecules also showed a trend with the severity of disease. We have found strong association between these factors upon their correlation and regression analysis. This study is a step toward understanding the indepth contribution of angiogenesis, inflammation and oxidative stress together in making BM microenvironment suitable for growth, survival and proliferation of malignant plasma cells in MM. |
Author | Khan, R. Kumar, L. Joshi, S. Gupta, N. Kumar, R. Sharma, A. Sharma, M. |
Author_xml | – sequence: 1 givenname: S. surname: Joshi fullname: Joshi, S. organization: Department of Biochemistry, All India Institute of Medical Sciences – sequence: 2 givenname: N. surname: Gupta fullname: Gupta, N. organization: Department of Biochemistry, All India Institute of Medical Sciences – sequence: 3 givenname: R. surname: Khan fullname: Khan, R. organization: Department of Biochemistry, All India Institute of Medical Sciences – sequence: 4 givenname: R. surname: Kumar fullname: Kumar, R. organization: Department of Biochemistry, All India Institute of Medical Sciences – sequence: 5 givenname: M. surname: Sharma fullname: Sharma, M. organization: Department of Radiation Oncology, Maulana Azad Medical College – sequence: 6 givenname: L. surname: Kumar fullname: Kumar, L. organization: Department of Medical Oncology, All India Institute of Medical Sciences – sequence: 7 givenname: A. surname: Sharma fullname: Sharma, A. email: dralpanasharma@gmail.com organization: Department of Biochemistry, All India Institute of Medical Sciences |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26169214$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1016/j.bbagen.2009.03.006 10.1155/2014/513170 10.1016/j.lfs.2004.05.021 10.2174/1381612811319150006 10.1113/jphysiol.2004.068114 10.4103/0022-3859.132319 10.1038/nature09421 10.1007/s00277-012-1572-5 10.1016/j.clinbiochem.2011.01.010 10.1158/1078-0432.CCR-06-2416 10.1111/j.1525-1438.2007.01089.x 10.1038/nm1351 10.1089/ars.2012.5149 10.1056/NEJMra1011442 10.1126/science.284.5422.1994 10.1172/JCI57322 10.1016/j.ejim.2006.02.012 10.1007/s00432-014-1731-2 10.1016/j.urolonc.2008.12.010 10.4103/0970-9185.130055 10.1159/000090949 10.1073/pnas.172161899 10.1007/s00535-011-0392-z 10.1007/s00011-012-0498-7 10.1080/10428190902802323 10.1016/j.devcel.2009.01.003 10.1080/09674845.2007.11732751 10.1007/s00277-002-0558-0 |
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Keywords | Angiogenesis Oxidative stress Inflammation Multiple myeloma Bone marrow microenvironment |
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Snippet | Background
Multiple myeloma (MM) is a B-cell malignancy characterized by the accumulation of clonal population of plasma cells in the bone marrow (BM). A... Multiple myeloma (MM) is a B-cell malignancy characterized by the accumulation of clonal population of plasma cells in the bone marrow (BM). A variety of... |
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SubjectTerms | Adult Aged Bone Marrow - pathology Enzyme-Linked Immunosorbent Assay Female Humans India Inflammation - pathology Male Medicine Medicine & Public Health Middle Aged Multiple Myeloma - blood supply Multiple Myeloma - pathology Neovascularization, Pathologic - pathology Oncology Oxidative Stress - physiology Research Article Tumor Microenvironment - physiology |
Title | Interrelationship between angiogenesis, inflammation and oxidative stress in Indian patients with multiple myeloma |
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