Biondi Antonio, Malaguarnera Giulia, Vacante Marco, Berretta Massimiliano, D'Agata Velia, Malaguarnera Michele, Basile Francesco, Drago Filippo, Bertino Gaetano
Department of General Surgery, Section of General Surgery and Oncology, Vittorio Emanuele Hospital, Via Plebiscito 628 University of Catania, 95123 Catania, Italy.
BMC Surg. 2012;12 Suppl 1(Suppl 1):S7. doi: 10.1186/1471-2482-12-S1-S7. Epub 2012 Nov 15.
During the past three decades, the incidence of hepatocellular carcinoma in the United States has tripled. The neuroendocrine character has been observed in some tumor cells within some hepatocellular carcinoma nodules and elevated serum chromogranin A also been reported in patients with hepatocellular carcinoma. The aim of this work was to investigate the role of serum concentration of chromogranin A in patients with hepatocellular carcinoma at different stages.
The study population consisted of 96 patients (63 males and 33 females age range 52-84) at their first hospital admission for hepatocellular carcinoma. The control group consisted of 35 volunteers (20 males and 15 females age range 50-80). The hepatocellular carcinoma patients were stratified according the Barcelona-Clinic Liver Cancer classification. Venous blood samples were collected before treatment from each patients before surgery, centrifuged to obtain serum samples and stored at -80° C until assayed.
The chromogranin A serum levels were elevated (> 100 ng/ml) in 72/96 patients with hepatocellular carcinoma. The serum levels of chromogranin A were significantly correlated (p<0.05) with alpha-fetoprotein. In comparison with controls, the hepatocellular carcinoma patients showed a significant increase (p<0.001) vs controls. The chromogranin A levels in the Barcelona staging of hepatocellular carcinoma was higher in stage D compared to stage C (p<0.01), to stage B (p<0.001), and to stage A (p<0.001).
Molecular markers, such as chromogranin A, could be very useful tools for hepatocellular carcinoma diagnosis. However the molecular classification should be incorporated into a staging scheme, which effectively separated patients into groups with homogeneous prognosis and response to treatment, and thus serves to aid in the selection of appropriate therapy.
在过去三十年中,美国肝细胞癌的发病率增长了两倍。在一些肝细胞癌结节内的部分肿瘤细胞中观察到了神经内分泌特征,并且也有报道称肝细胞癌患者血清嗜铬粒蛋白A水平升高。这项研究的目的是调查不同阶段肝细胞癌患者血清嗜铬粒蛋白A浓度的作用。
研究对象包括96例因肝细胞癌首次入院的患者(63例男性,33例女性,年龄范围52 - 84岁)。对照组由35名志愿者组成(20例男性,15例女性,年龄范围50 - 80岁)。肝细胞癌患者根据巴塞罗那临床肝癌分类进行分层。在治疗前、手术前从每位患者采集静脉血样本,离心获得血清样本并储存在 -80°C直至检测。
96例肝细胞癌患者中有72例(>100 ng/ml)血清嗜铬粒蛋白A水平升高。血清嗜铬粒蛋白A水平与甲胎蛋白显著相关(p<0.05)。与对照组相比,肝细胞癌患者血清嗜铬粒蛋白A水平显著升高(p<0.001)。在肝细胞癌的巴塞罗那分期中,D期的嗜铬粒蛋白A水平高于C期(p<0.01)、B期(p<0.001)和A期(p<0.001)。
诸如嗜铬粒蛋白A等分子标志物可能是肝细胞癌诊断的非常有用的工具。然而,分子分类应纳入分期方案,该方案能有效地将患者分为预后和对治疗反应均一的组,从而有助于选择合适的治疗方法。