Serum macrophage-colony stimulating factor levels in colorectal cancer patients correlate with lymph node metastasis and poor prognosis

被引:86
作者
Mroczko, Barbara
Groblewska, Magdalena
Wereszczynska-Siemiatkowska, Urszula
Okulczyk, Bogna
Kedra, Boguslaw
Laszewicz, Wiktor
Dabrowski, Andrzej
Smitkowski, Maciej
机构
[1] Med Univ, Dept Biochem Diagnost, PL-15276 Bialystok, Poland
[2] Med Univ, Dept Gastroenterol, Bialystok, Poland
[3] Med Univ, Dept Gen Surg 2, Bialystok, Poland
关键词
M-CSF; serum; colorectal cancer; prognosis; survival;
D O I
10.1016/j.cca.2007.02.037
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Elevated serum concentrations of macrophage-colony stimulating factor (M-CSF) have been found in a variety of malignant diseases. The aim of our study was to assess correlations between serum levels of M-CSF and clinicopathological features and survival rates in patients with colorectal cancer (CRC). Patients/methods: M-CSF and the established tumor markers (carcinoembryonic antigen - CEA and carbohydrate antigen - CA 19-9) were investigated in the sera of 116 colorectal cancer patients and correlated with the clinical parameters of the disease and with the survival of patients. We compared M-CSF serum levels in CRC with colorectal adenoma patients. M-CSF was determined using enzyme-linked immunosorbent assay (ELISA). Tumor markers were measured by microparticle enzyme immunoassays (MEIA). Results: CRC patients had significantly higher M-CSF and tumor markers levels compared to healthy controls and colorectal adenoma patients, with a significant association between M-CSF levels, disease stage and lymph node metastasis. Serum levels of M-CSF and CEA decreased significantly after radical resection of the tumor. Moreover, the multivariate analysis showed that the serum level of M-CSF in CRC patients was an independent prognostic factor. Conclusion: These findings suggest the potential clinical use of circulating M-CSF measurements, particularly in estimating prognosis for patients with CRC. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:208 / 212
页数:5
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