BMC Cancer | |
Downregulation of GPR155 as a prognostic factor after curative resection of hepatocellular carcinoma | |
Shinichi Umeda1  Masamichi Hayashi1  Yasuhiro Kodera1  Mitsuro Kanda1  Naoki Iwata1  Haruyoshi Tanaka1  Daisuke Kobayashi1  Yukiko Niwa1  Chie Tanaka1  Suguru Yamada1  Tsutomu Fujii1  Hiroyuki Sugimoto1  Hideki Takami1  Michitaka Fujiwara1  | |
[1] Department of Gastroenterological Surgery (Surgery II), Nagoya University Graduate School of Medicine; | |
关键词: Hepatocellular carcinoma; GPR155; Expression; Recurrence; Biomarker; | |
DOI : 10.1186/s12885-017-3629-2 | |
来源: DOAJ |
【 摘 要 】
Abstract Background Molecular biomarkers capable of predicting recurrence patterns and prognosis are helpful for risk stratification and providing appropriate treatment to patients with hepatocellular carcinoma (HCC). In this study, we focused on G protein-coupled receptor 155 (GPR155), a cell surface signaling protein, as a candidate biomarker. Methods We analyzed GPR155 expression, DNA methylation, and copy number in HCC cell lines. The clinical significance of GPR155 expression was evaluated using 144 pairs of surgically resected liver and normal tissues with subgroup analysis based on hepatitis virus infection. Results GPR155 mRNA expression levels were differential and were decreased in 89% of HCC cell lines. No DNA methylation was detected, whereas copy number alterations were present in five (56%) HCC cell lines. GPR155 mRNA expression level was independent of background liver status and significantly lower in HCC tissues than corresponding normal liver tissues. The expression patterns of GPR155 protein by immunohistochemical staining were significantly associated with those of GPR155 mRNA. Downregulation of GPR155 was significantly associated with more aggressive HCC phenotypes including high preoperative α-fetoprotein, poor differentiation, serosal infiltration, vascular invasion, and advanced disease stage. Patients with downregulation of GPR155 were more likely to have worse prognosis after curative resection irrespective of hepatitis virus infection. Patients who experienced extrahepatic (distant) recurrences had significantly lower GPR155 expression than those with intrahepatic (liver confined) recurrences. Conclusions Downregulation of GPR155 may serve as a prognosticator that also predicts initial recurrence sites independent of hepatitis virus infection.
【 授权许可】
Unknown