Goldman Radoslav, Ressom Habtom W, Abdel-Hamid Mohamed, Goldman Lenka, Wang Antai, Varghese Rency S, An Yanming, Loffredo Christopher A, Drake Steven K, Eissa Sohair A, Gouda Iman, Ezzat Sameera, Moiseiwitsch Francoise Seillier
Georgetown University, Lombardi Comprehensive Cancer Center, 3970 Reservoir Road Northwest, Washington, DC 20057, USA.
Carcinogenesis. 2007 Oct;28(10):2149-53. doi: 10.1093/carcin/bgm177. Epub 2007 Aug 27.
Hepatocellular carcinoma (HCC) represents an important public health problem in Egypt where up to 90% of HCC cases are attributable to hepatitis C viral (HCV) infection. Serum alpha-fetoprotein is elevated in only approximately 60% of HCC patients. The development of effective markers for the detection of HCC could have an impact on cancer mortality and significant public health implications worldwide. The objective of our study was to assess six candidate markers for detection of HCC identified by mass spectrometric analysis of enriched serum. The study examined 78 HCC cases and 72 age- and gender-matched cancer-free controls recruited from the Egyptian population. Matrix-assisted laser desorption-ionization time-of-flight mass spectrometric analysis of enriched low-molecular weight fraction of serum was used for identification of the candidate markers. Our analyses show that all six candidate markers are associated with HCC after adjustment for important covariates including HCV and hepatitis B viral infections. The marker candidates are independently predictive of HCC with areas under the receiver operating characteristic (AuROC) curve ranging from 63-93%. A combination of the six markers improves prediction accuracy to 100% sensitivity, 91% specificity and 98% AuROC curve in an independent test set of 50 patients. Two of the candidate markers were identified by sequencing as fragments of complement C3 and C4. In conclusion, a set of six peptides distinguished with high prediction accuracy HCC from controls in an Egyptian population with a high rate of chronic HCV infection. Further evaluation of these marker candidates for the diagnosis of HCC is needed.
肝细胞癌(HCC)是埃及一个重要的公共卫生问题,在埃及,高达90%的HCC病例归因于丙型肝炎病毒(HCV)感染。仅约60%的HCC患者血清甲胎蛋白升高。开发有效的HCC检测标志物可能会对癌症死亡率产生影响,并在全球范围内具有重大的公共卫生意义。我们研究的目的是评估通过富集血清的质谱分析确定的六个HCC检测候选标志物。该研究检查了从埃及人群中招募的78例HCC病例和72例年龄和性别匹配的无癌对照。采用基质辅助激光解吸电离飞行时间质谱分析富集的血清低分子量组分,以鉴定候选标志物。我们的分析表明,在对包括HCV和乙型肝炎病毒感染在内的重要协变量进行调整后,所有六个候选标志物均与HCC相关。候选标志物可独立预测HCC,受试者操作特征(AuROC)曲线下面积范围为63%-93%。在一个由50名患者组成的独立测试集中,六个标志物的组合将预测准确率提高到100%的灵敏度、91%的特异性和98%的AuROC曲线。通过测序鉴定出两个候选标志物为补体C3和C4的片段。总之,在慢性HCV感染率较高的埃及人群中,一组六个肽段以高预测准确率区分了HCC和对照。需要进一步评估这些候选标志物用于HCC诊断的价值。