Evaluation of serum amyloid A as a biomarker for gastric cancer

被引:103
作者
Chan, De-Chuan [1 ]
Chen, Cheng-Jueng
Chu, Heng-Cheng
Chang, Wei-Kuo
Yu, Jyh-Cherng
Chen, Yu-Ju
Wen, Li-Li
Huang, Su-Ching
Ku, Chih-Hung
Liu, Yao-Chi
Chen, Jenn-Han
机构
[1] Natl Def Med Ctr, Tri Serv Gen Hosp, Div Gen Surg, Taipei, Taiwan
[2] Natl Def Med Ctr, Tri Serv Gen Hosp, Div Gastroenterol, Taipei, Taiwan
[3] Acad Sinica, Inst Chem, Taipei, Taiwan
[4] En Chu Kong Hosp, Dept Clin Lab, Taipei, Taiwan
[5] Natl Def Univ, Natl Def Med Ctr, Tri Serv Gen Hosp, Dept Dent, Taipei 114, Taiwan
[6] Natl Def Med Ctr, Sch Publ Hlth, Taipei, Taiwan
关键词
serum amyloid A (SAA) protein; stomach neoplasm; serum marker; mass spectrometry (MS);
D O I
10.1245/s10434-006-9091-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Serum amyloid A (SAA) is a useful biomarker for gastric cancer in an animal model. We investigated the potential of SAA as a biomarker for gastric cancer in humans. Methods: Serum levels of SAA from 96 gastric cancer patients were measured before and after curative gastrectomy; 32 patients with gastric ulcers and 52 healthy subjects were the control groups. The immunohistochemical study was performed to evaluate the protein expression over gastric cancer tissue slides. Results: The mean SAA concentration was higher in gastric cancer patients (88.54 +/- 50.44 mg/l) than in healthy subjects (3.36 +/- 2.29 mg/l) and gastric ulcer patients (10.48 +/- 8.97 mg/l) (P < .05). The SAA concentration was associated with tumor stage (P = .0244) and location (P = .0016) but not with Lauren's histological type (P = .839). In the multivariate analysis, SAA level was correlated with tumor location (P < .0001) and lymph node status (P < .05). During follow-up, the mean SAA concentration increased significantly in 24 patients with tumor recurrence (P < .05) but did not change in 77 patients without recurrence. In the survival analysis, patients with SAA levels > 97 mg/l had a nearly fourfold increase in risk of death. Immunoreactivity was most prominent in blood vessel regions but not within cancer cells. Conclusions: These data not only demonstrated SAA was useful in predicting survival of patients with gastric cancer, but they also showed that SAA was a valuable tool for postoperative follow-up.
引用
收藏
页码:84 / 93
页数:10
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