Institute of Public Health, School of Medicine, National Yang-Ming University, Taipei, Taiwan, ROC.
Anticancer Res. 2013 Jun;33(6):2763-9.
Glycine N-methyltransferase (GNMT) is a tumor suppressor of hepatocellular carcinoma (HCC). High proportions of GNMT knockout mice developed HCC. We previously identified a potential novel marker from Gnmt knockout mice, FK506 binding protein 11 (FKBP11). Here, we determined the clinical usefulness of FKBP11.
FKBP11 expression levels were analyzed in 123 paired tumor and tumor-adjacent non-tumorous (TA) tissue samples from patients with HCC and in 29 benign liver samples from patients with hemangioma using quantitative real-time polymerase-chain-reaction.
FKBP11 was expressed at a higher level in tumor tissues compared to TA tissues (p<0.01). Moreover, we observed a significantly higher level of FKBP11 in TA tissues than in benign liver samples (p<0.01). Interestingly, expression of FKBP11 was higher in hepatitis viral-infected TA and benign tissues than in samples without viral etiology (p<0.05).
These results suggest a progressively elevated expression of FKBP11 during the development of HCC and FKBP11 has the potential to be an early marker for HCC.
甘氨酸 N-甲基转移酶(GNMT)是肝细胞癌(HCC)的肿瘤抑制因子。高比例的 GNMT 敲除小鼠发展为 HCC。我们之前从 Gnmt 敲除小鼠中鉴定出一种潜在的新型标志物 FK506 结合蛋白 11(FKBP11)。在这里,我们确定了 FKBP11 的临床用途。
使用实时定量聚合酶链反应分析了 123 对来自 HCC 患者的肿瘤和肿瘤相邻非肿瘤(TA)组织样本以及 29 对来自血管瘤患者的良性肝样本中的 FKBP11 表达水平。
与 TA 组织相比,肿瘤组织中 FKBP11 的表达水平更高(p<0.01)。此外,我们观察到 TA 组织中 FKBP11 的水平明显高于良性肝样本(p<0.01)。有趣的是,在乙型肝炎病毒感染的 TA 和良性组织中,FKBP11 的表达高于无病毒病因的样本(p<0.05)。
这些结果表明,FKBP11 在 HCC 的发展过程中表达逐渐升高,并且 FKBP11 有可能成为 HCC 的早期标志物。