AI Article Synopsis

  • Previous research has indicated changes in cytokine levels in cancer patients, which this study aimed to explore further.
  • The serum levels of specific cytokines (SCF, IL-3, M-CSF, GM-CSF) were measured in 40 pancreatic and ampullary cancer patients compared to 40 healthy volunteers, along with traditional tumor markers (CA 19-9, CEA).
  • The study found that M-CSF and SCF showed significant differences in levels between cancer patients and controls, with M-CSF showing high diagnostic sensitivity, suggesting it could be a valuable tumor marker in future research.

Article Abstract

Background: Previous studies have demonstrated altered levels of hematopoietic cytokines in the serum of patients with different types of cancer.

Methods: We measured the serum levels of the hematopoietic cytokines stem cell factor (SCF), interleukin 3 (IL-3), macrophage-colony stimulating factor (M-CSF) and granulocyte-macrophage-colony stimulating factor (GM-CSF) in 40 pancreatic and ampullary cancer patients and 40 healthy volunteers, using ELISA. We also assessed the most widely used pancreatic tumor markers, carbohydrate antigen 19-9 (CA 19-9) and carcinoembryonic antigen (CEA), in both groups. We then correlated the concentrations of the cytokines' and the tumor markers in the patients' serum and we estimated their diagnostic ability by calculating diagnostic sensitivity and specificity, positive and negative predictive values and the receiver operating characteristic (ROC) curve.

Results: The SCF and IL-3 levels were significantly lower and the M-CSF levels significantly higher in pancreatic cancer patients than in controls. There were significant positive correlations between the serum levels of CEA and M-CSF, GM-CSF and SCF, and between GM-CSF and IL-3. The area under the ROC curve and diagnostic sensitivity of M-CSF were greater than those of SCF and IL-3. The diagnostic sensitivity of the combined use of SCF and M-CSF reached 97.5%.

Conclusion: The diagnostic ability of M-CSF and SCF in pancreatic and ampullary cancer should stimulate further studies evaluating their clinical usefulness as tumor markers.

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Source
http://dx.doi.org/10.5301/JBM.2012.9348DOI Listing

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