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Serum macrophage migration‐inhibitory factor as a diagnostic and prognostic biomarker for gastric cancer
Authors:Harry Hua‐Xiang Xia PhD  Yi Yang PhD  Kent‐Man Chu MBBS  MS  Qing Gu PhD  Yuan‐Yuan Zhang PhD  Hua He MPhil  Wai Man Wong MD  PhD  Suet‐Yi Leung MD  Siu‐Tsan Yuen MBBS  Man‐Fung Yuen MD  PhD  Annie O.O. Chan MD  PhD  Benjamin C.Y. Wong MD  PhD
Affiliation:1. Department of Medicine, University of Hong Kong, Hong Kong, China;2. HHX Xia's current address is Senior Medical Scientific Expert of Novartis Pharmaceuticals Corporation, East Hanover, New Jersey;3. Y. Yang, postdoctoral fellow at McKusick‐Nathans Institute of Genetic Medicine, Johns Hopkins University, Baltimore, Maryland;4. and H. He, English editor of the Chinese Journal of Cancer, Guangzhou, China.;5. Department of Surgery, University of Hong Kong, Hong Kong, China;6. Department of Microbiology and Microbial Engineering, School of Life Sciences, Fudan University, Shanghai, China;7. Department of Pathology, University of Hong Kong, Hong Kong, China;8. Fax: (011) 852‐2904 9443
Abstract:

BACKGROUND:

This study aimed to determine the potential diagnostic value of migration‐inhibitory factor (MIF) for gastric cancer in patients presenting with dyspepsia and its prognostic value for gastric cancer.

METHODS:

A cohort of 97 patients with histologically confirmed gastric adenocarcinoma and 222 patients with dyspepsia were recruited. Enzyme‐linked immunosorbent assay was used to measure serum MIF and carcinoembryonic antigen (CEA).

RESULTS:

The serum MIF concentrations were 6554.0 ± 204.1 pg/mL and 1453.7 ± 79.9 pg/mL, respectively, in gastric cancer patients and dyspeptic patients (P < .001). Serum MIF levels increased with the advancing gastric pathologies (P < .001). With the cutoff value of 3230 pg/mL, serum MIF had sensitivity, specificity, and accuracy of 83.5%, 92.3%, and 89.7%, respectively, in diagnosing gastric cancer, whereas the rates were 60.8%, 83.3%, and 76.5%, respectively, for serum CEA. Gastric cancer patients with serum MIF levels above 6600 pg/mL had a lower 5‐year survival rate than those with serum MIF level below that level (P = .012). Higher serum CEA levels were also associated with poor survival. The prediction for 5‐year survival was even better (P = .0001), using a combination of serum MIF and CEA.

CONCLUSIONS:

Serum MIF level, which correlates with gastric MIF expression, is a better molecular marker than CEA in diagnosing gastric cancer in patients presenting with dyspepsia. A combination of serum MIF and CEA predicts 5‐year survival better than the individual test. Cancer 2009. © 2009 American Cancer Society.
Keywords:macrophage migration‐inhibitory factor  carcinoembryonic antigen  gastric cancer  diagnosis  prognosis
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