Expression and therapeutic potential of macrophage migration inhibitory factor and CD74 in ovarian cancer
1Department of Obstetrics and Gynecology, Daejeon (Republic of Korea)
2Department of General Surgery, College of Medicine, The Catholic University of Korea, Seocho-gu, Seoul
3Department of Pathology, Bucheon St. Mary’s Hospital, College of Medicine,The Catholic University of Korea, Wonmi-gu, Bucheon, Gyeonggi-do
4Department of Pathology, Daejeon St. Mary’s Hospital, College of Medicine, The Catholic University of Korea,Jung-gu, Daejeon (Republic of Korea)
DOI: 10.31083/j.ejgo.2020.01.4887 Vol.41,Issue 1,February 2020 pp.65-69
Published: 15 February 2020
Purpose of Investigation: To evaluate macrophage migration inhibitory factor (MIF) and CD74 expression in ovarian cancer, and to explore whether these expression levels correlate with clinicopathologic parameters. Materials and Methods: A total of 151 tissue samples were collected from May 2009 through May 2015. The collected samples included ten normal ovaries, 41 benign epithelial ovarian tumors, 38 borderline tumors, and 62 malignant epithelial ovarian tumors. CD74 and MIF expression was assessed by immunohistochemistry and a retrospective study was conducted. Results: Immunohistochemical analysis showed that MIF and CD74 expression was significantly higher in ovarian tumors, including ovarian cancer, than in normal ovary tissues. Furthermore, high MIF expression was correlated with lymph node metastasis (p = 0.048) and ovary surface invasion (p = 0.039). Conclusion: The present findings suggest that co-expression of MIF and CD74 in ovarian cancer is associated with poor clinical parameters and may serve as a therapeutic target for the treatment of ovarian cancer
Ovarian tumor; CD74; Macrophage migration inhibitory factor (MIF); Immunohistochemistry
Y. S. Lee,J. M. Baek,E. K. Park,C. J. Kim,H. J. Lee,J. O. Kim. Expression and therapeutic potential of macrophage migration inhibitory factor and CD74 in ovarian cancer. European Journal of Gynaecological Oncology. 2020. 41(1);65-69.
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