Pontisso Patrizia
Department of Medicine, University of Padua, Italy.
Ann Hepatol. 2014 Nov-Dec;13(6):722-7.
SERPINB3 (formerly known as squamous cell carcinoma antigen-1 or SCCA1) is a member of the family of serine-protease inhibitors. SERPINB3 protects cells from oxidative stress conditions, but in chronic liver damage this serpin may lead to hepatocellular carcinoma through different strategies, including inhibition of apoptosis, induction of epithelial to mesenchymal transition and decrease of desmosomal junctions, cell proliferation and invasiveness. SERPINB3 may also contribute to tumor cell resistance to anti-neoplastic drugs through its binding to the respiratory Complex I, protecting cells from the pro-oxidant action of chemotherapeutic agents. Mechanisms of tumor growth promotion induced by SERPINB3 include the inhibition of intratumor infiltration of natural killer cells, up-regulation of Myc oncogene and the recent identification of this serpin as a Ras-responsive factor. In the liver SERPINB3 and SERPINBB4 isoforms (known as squamous cell carcinoma antigen or SCCA) are undetectable in normal hepatocytes, but their expression progressively increases in chronic liver diseases, dysplastic nodules and hepatocellular carcinoma. High SERPINB3 levels have been recently detected in HCC tissue of patients with early tumor recurrence after surgical resection. In serum SERPINB3/4 isoforms (or SCCA) are detectable bound to IgMs (SCCA-IgM) in the majority of HCV infected patients with HCC and in patients with cirrhosis their levels and/or the progressive increase have been found correlated to the risk of HCC development. Preliminary findings in patients with HCC revealed that SCCA-IgM was predictive of HCC prognosis, since low levels of this biomarker were able to identify HCC patients with long overall and progression-free survival.
丝氨酸蛋白酶抑制剂B3(以前称为鳞状细胞癌抗原-1或SCCA1)是丝氨酸蛋白酶抑制剂家族的成员。丝氨酸蛋白酶抑制剂B3保护细胞免受氧化应激条件的影响,但在慢性肝损伤中,这种丝氨酸蛋白酶抑制剂可能通过不同策略导致肝细胞癌,包括抑制细胞凋亡、诱导上皮-间质转化以及减少桥粒连接、细胞增殖和侵袭性。丝氨酸蛋白酶抑制剂B3还可能通过与呼吸复合体I结合,使肿瘤细胞对抗肿瘤药物产生耐药性,保护细胞免受化疗药物的促氧化作用。丝氨酸蛋白酶抑制剂B3诱导肿瘤生长促进的机制包括抑制自然杀伤细胞的肿瘤内浸润、上调Myc癌基因以及最近将这种丝氨酸蛋白酶抑制剂鉴定为Ras反应因子。在肝脏中,正常肝细胞中检测不到丝氨酸蛋白酶抑制剂B3和丝氨酸蛋白酶抑制剂B4亚型(称为鳞状细胞癌抗原或SCCA),但它们在慢性肝病、发育异常结节和肝细胞癌中的表达逐渐增加。最近在手术切除后早期肿瘤复发患者的肝癌组织中检测到高丝氨酸蛋白酶抑制剂B3水平。在血清中,大多数丙型肝炎病毒感染的肝癌患者以及肝硬化患者中可检测到与IgM结合的丝氨酸蛋白酶抑制剂B3/4亚型(或SCCA)(SCCA-IgM),其水平和/或逐渐升高与肝癌发生风险相关。肝癌患者的初步研究结果显示,SCCA-IgM可预测肝癌预后,因为这种生物标志物水平较低能够识别总体生存期和无进展生存期较长的肝癌患者。