Expression of serum amyloid A, in normal, dysplastic, and neoplastic human colonic mucosa: Implication for a role in colonic tumorigenesis

被引:74
作者
Gutfeld, O
Prus, D
Ackerman, Z
Dishon, S
Linke, RP
Levin, M
Urieli-Shoval, S [1 ]
机构
[1] Hadassah Hebrew Univ, Med Ctr, Hematol Unit, IL-91240 Jerusalem, Israel
[2] Hadassah Hebrew Univ, Med Ctr, Dept Oncol, IL-91240 Jerusalem, Israel
[3] Hadassah Hebrew Univ, Med Ctr, Dept Pathol, IL-91240 Jerusalem, Israel
[4] Hadassah Hebrew Univ, Med Ctr, Dept Internal Med, IL-91240 Jerusalem, Israel
[5] Max Planck Inst Biochem, D-82152 Martinsried, Germany
关键词
serum amyloid A; colon tissues; colonic neoplasia;
D O I
10.1369/jhc.5A6645.2005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Serum amyloid A (SAA) is an acute phase reactant, whose level in the blood is elevated in response to trauma, infection, inflammation, and neoplasia. Elevated levels of SAA in the serum of cancer patients were suggested to be of liver origin rather than a tumor cell product. The role of SAA in human malignancies has not been elucidated. We investigated the expression of SAA at various stages of human colon carcinoma progression. Nonradioactive in situ hybridization applied on paraffin tissue sections from 26 colon cancer patients revealed barely detected SAA mRNA expression in normal looking colonic epithelium. Expression was increased gradually as epithelial cells progressed through dysplasia to neoplasia. Deeply invading colon carcinoma cells showed the highest levels of SAA. Expression was also found in colon carcinoma metastases. Cells of lymphoid follicles of the intestinal wall, inflammatory cells, ganglion cells, and endothelial cells, also expressed SAA mRNA. Immunohistochemical staining revealed SAA protein expression that colocalized with SAA mRNA expression. RT-PCR analysis confirmed the expression of the SAA1 and SAA4 genes in colon carcinomas, expression that was barely detectable in normal colon tissues. These findings indicate local and differential expression of SAA in human colon cancer tissues and suggest its role in colonic tumorigenesis.
引用
收藏
页码:63 / 73
页数:11
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