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. 2014:2014:274584.
doi: 10.1155/2014/274584. Epub 2014 May 27.

HLA-G expression is an independent predictor for improved survival in high grade ovarian carcinomas

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HLA-G expression is an independent predictor for improved survival in high grade ovarian carcinomas

M J Rutten et al. J Immunol Res. 2014.

Abstract

Aberrant expression of human leukocyte antigens (HLA) class I has prognostic importance in various cancers. Here, we evaluated the prognostic value of classical (A/B/C) and nonclassical (G/E) HLA expression in 169 high grade epithelial ovarian cancer samples and linked that to clinicopathological characteristics and survival. Expression of HLA-A, -B/C, or -E was not correlated with survival. Survival was prolonged when tumours expressed HLA-G (P = 0.008) and HLA-G was an independent predictor for better survival (P = 0.011). In addition, HLA-G expression was associated with longer progression-free survival (P = 0.036) and response to chemotherapy (P = 0.014). Accordingly, high expression of HLA-G mRNA was associated with prolonged disease-free survival (P = 0.037) in 65 corresponding samples. Elevated serum-soluble HLA-G levels as measured by enzyme-linked immunosorbent assay in 50 matched patients were not correlated to HLA-G protein expression or gene expression nor with survival. During treatment, sHLA-G levels declined (P = 0.038). In conclusion, expression of HLA-G is an independent prognostic factor for improved survival in high grade epithelial ovarian cancer and a predictor for platinum sensitivity.

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Figures

Figure 1
Figure 1
Representative examples of HLA immunohistochemical staining, HLA-A ((a)–(c)), HLA-B/C ((d)–(f)), HLA-E ((h)–(j)), and HLA-G ((i)-(j)). Strong expression ((a), (d), (g), and (i)), weak expression ((b) and (e)), and loss of expression ((c), (f), (h), and (j)).
Figure 2
Figure 2
Survival analyses. Kaplan-Meier 5-year survival curves and log-rank test for HLA-G expression (a), HLA-A expression (b), HLA-G expression in tumours with downregulation of HLA-A (c), and HLA-G gene expression at the median expression cut-off of 230.4 fluorescence units (d) (NS = not significant).
Figure 3
Figure 3
Median concentration of sHLA-G (u/mL) at diagnosis, after 2 cycles of chemotherapy, after primary treatment, and at recurrence. ⊥ is the lowest interquartile and is the highest interquartile.

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References

    1. Siegel R, Naishadham D, Jemal A. Cancer statistics, 2012. CA Cancer Journal for Clinicians. 2012;62(1):10–29. - PubMed
    1. Elattar A, Bryant A, Winter-Roach BA, Hatem M, Naik R. Optimal primary surgical treatment for advanced epithelial ovarian cancer. Cochrane Database of Systematic Reviews. 2011;(8):p. CD007565. - PMC - PubMed
    1. Braicu E-I, Sehouli J, Richter R, Pietzner K, Denkert C, Fotopoulou C. Role of histological type on surgical outcome and survival following radical primary tumour debulking of epithelial ovarian, fallopian tube and peritoneal cancers. British Journal of Cancer. 2011;105(12):1818–1824. - PMC - PubMed
    1. Winter WE, III, Maxwell GL, Tian C, et al. Tumor residual after surgical cytoreduction in prediction of clinical outcome in stage IV epithelial ovarian cancer: a Gynecologic Oncology Group study. Journal of Clinical Oncology. 2008;26(1):83–89. - PubMed
    1. Kurman RJ, Shih I-M. Molecular pathogenesis and extraovarian origin of epithelial ovarian cancer—shifting the paradigm. Human Pathology. 2011;42(7):918–931. - PMC - PubMed

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