| Literature DB >> 27739028 |
Hao Xing1, Cunling Yan2, Liming Cheng3, Nianyue Wang4, Shuyang Dai1, Jianyong Yuan1, Wenfeng Lu1, Zhouchong Wang1, Jun Han1, Yijie Zheng5, Tian Yang6.
Abstract
Hepatocellular carcinoma (HCC) is the third leading cause of cancer deaths worldwide. Early diagnosis improves the prognosis. Protein induced by vitamin K antagonist-II (PIVKA-II) is an effective serum biomarker for HCC diagnosis and prognosis. Combined with another serum biomarker α-fetoprotein (AFP), the sensitivity and specificity of HCC diagnosis can be improved to a maximum of 94 and 98.5 %, respectively. PIVKA-II alone or in combination with AFP and/or AFP-L3 was effective in predicting the treatment response and clinical outcome of curative hepatic resection, chemotherapy, targeted therapy, radiotherapy, and liver transplantation. Japanese clinical guidelines recommend the combined use of PIVKA-II and AFP for the diagnosis of HCC, management of high-risk population, and prognosis of anticancer treatment. Further, PIVKA-II as a functional target promoted HCC cell proliferation, invasion, and metastasis by activating c-Met and other signal transduction pathways. Inhibition of PIVKA-II may provide a selective and effective therapy for HCC.Entities:
Keywords: Biomarker; Diagnosis; Hepatocellular carcinoma; Protein induced by vitamin K antagonist-II; Treatment outcome
Year: 2016 PMID: 27739028 DOI: 10.1007/s13277-016-5443-x
Source DB: PubMed Journal: Tumour Biol ISSN: 1010-4283