Xu Michelle Z, Yao Tzy-Jyun, Lee Nikki P Y, Ng Irene O L, Chan Yuk-Tat, Zender Lars, Lowe Scott W, Poon Ronnie T P, Luk John M
Department of Surgery and Center for Cancer Research, the University of Hong Kong, Pokfulam, Hong Kong.
Cancer. 2009 Oct 1;115(19):4576-85. doi: 10.1002/cncr.24495.
Yes-associated protein (YAP), a downstream target of the Hippo signaling pathway, was recently linked to hepatocarcinogenesis in a mouse hepatocellular carcinoma (HCC) model. The objective of the current study was to investigate the clinical significance of YAP in HCC and its prognostic values in predicting survival and tumor recurrence.
The authors collected 177 pairs of tumor and adjacent nontumor tissue from HCC patients with definitive clinicopathologic and follow-up data. YAP expression was determined by immunohistochemistry, Western blot analysis, and quantitative polymerase chain reaction. Association of YAP with each clinicopathologic feature was analyzed by Pearson chi-square test, and HCC-specific disease-free survival and overall survival by Kaplan-Meier curves and log-rank test. Multivariate Cox regression analyses of YAP in HCC were also performed.
YAP was expressed in the majority of HCC cases (approximately 62%) and mainly accumulated in the tumor nucleus. Overexpression of YAP in HCC was significantly associated with poorer tumor differentiation (Edmonson grade; P = .021) and high serum alpha-fetoprotein (AFP) level (P < .001). Kaplan-Meier and Cox regression data indicated that YAP was an independent predictor for HCC-specific disease-free survival (hazards ratio [HR], 1.653; 95% confidence interval [95% CI], 1.081-2.528 [P = .02]) and overall survival (HR, 2.148; 95% CI, 1.255-3.677 [P = .005]).
YAP is an independent prognostic marker for overall survival and disease-free survival times of HCC patients and clinicopathologically associated with tumor differentiation and serum AFP level. It is a potential therapeutic target for this aggressive malignancy.
Yes相关蛋白(YAP)是Hippo信号通路的下游靶点,最近在小鼠肝细胞癌(HCC)模型中与肝癌发生相关。本研究的目的是探讨YAP在HCC中的临床意义及其在预测生存和肿瘤复发方面的预后价值。
作者收集了177对来自HCC患者的肿瘤组织和癌旁非肿瘤组织,并具有明确的临床病理和随访数据。通过免疫组织化学、蛋白质印迹分析和定量聚合酶链反应来确定YAP的表达。采用Pearson卡方检验分析YAP与各临床病理特征的相关性,采用Kaplan-Meier曲线和对数秩检验分析HCC特异性无病生存期和总生存期。还对HCC中的YAP进行了多因素Cox回归分析。
YAP在大多数HCC病例中表达(约62%),且主要在肿瘤细胞核中积聚。HCC中YAP的过表达与较差的肿瘤分化(Edmonson分级;P = 0.021)和高血清甲胎蛋白(AFP)水平(P < 0.001)显著相关。Kaplan-Meier和Cox回归数据表明,YAP是HCC特异性无病生存期(风险比[HR],1.653;95%置信区间[95%CI],1.081 - 2.528 [P = 0.02])和总生存期(HR,2.148;95%CI,1.255 - 3.677 [P = 0.005])的独立预测因子。
YAP是HCC患者总生存期和无病生存期的独立预后标志物,在临床病理上与肿瘤分化和血清AFP水平相关。它是这种侵袭性恶性肿瘤的潜在治疗靶点。