Stanojevic Boban, Saenko Vladimir, Todorovic Lidija, Petrovic Nina, Nikolic Dragan, Zivaljevic Vladan, Paunovic Ivan, Nakashima Masahiro, Yamashita Shunichi, Dzodic Radan
Atomic Bomb Disease Institute, Nagasaki University, Nagasaki, Japan; Laboratory for Radiobiology and Molecular Genetics, "Vinca" Institute of Nuclear Sciences, University of Belgrade, Belgrade, Serbia.
Atomic Bomb Disease Institute, Nagasaki University, Nagasaki, Japan.
PLoS One. 2014 Dec 9;9(12):e114511. doi: 10.1371/journal.pone.0114511. eCollection 2014.
Alterations of the von Hippel-Lindau (VHL) tumor suppressor gene can cause different hereditary tumors associated with VHL syndrome, but the potential role of the VHL gene in papillary thyroid carcinoma (PTC) has not been characterized. This study set out to investigate the relationship of VHL expression level with clinicopathological features of PTC in an ethnically and geographically homogenous group of 264 patients from Serbia, for the first time. Multivariate logistic regression analysis showed a strong correlation between low level of VHL expression and advanced clinical stage (OR = 5.78, 95% CI 3.17-10.53, P<0.0001), classical papillary morphology of the tumor (OR = 2.92, 95% CI 1.33-6.44, P = 0.008) and multifocality (OR = 1.96, 95% CI 1.06-3.62, P = 0.031). In disease-free survival analysis, low VHL expression had marginal significance (P = 0.0502 by the log-rank test) but did not appear to be an independent predictor of the risk for chance of faster recurrence in a proportion hazards model. No somatic mutations or evidence of VHL downregulation via promoter hypermethylation in PTC were found. The results indicate that the decrease of VHL expression associates with tumor progression but the mechanism of downregulation remains to be elucidated.
冯·希佩尔-林道(VHL)肿瘤抑制基因的改变可导致与VHL综合征相关的不同遗传性肿瘤,但VHL基因在甲状腺乳头状癌(PTC)中的潜在作用尚未明确。本研究首次在来自塞尔维亚的264名种族和地域同质的患者中,探讨VHL表达水平与PTC临床病理特征之间的关系。多因素逻辑回归分析显示,VHL低表达与临床晚期(OR = 5.78,95%CI 3.17 - 10.53,P<0.0001)、肿瘤的经典乳头状形态(OR = 2.92,95%CI 1.33 - 6.44,P = 0.008)和多灶性(OR = 1.96,95%CI 1.06 - 3.62,P = 0.031)密切相关。在无病生存分析中,VHL低表达具有边缘显著性(对数秩检验P = 0.0502),但在比例风险模型中似乎不是复发风险增加的独立预测因素。未发现PTC中有体细胞突变或通过启动子高甲基化导致VHL下调的证据。结果表明,VHL表达降低与肿瘤进展相关,但其下调机制仍有待阐明。