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维生素K拮抗剂-II诱导蛋白作为生物标志物在肝细胞癌中的临床应用

Clinical application of protein induced by vitamin K antagonist-II as a biomarker in hepatocellular carcinoma.

作者信息

Xing Hao, Yan Cunling, Cheng Liming, Wang Nianyue, Dai Shuyang, Yuan Jianyong, Lu Wenfeng, Wang Zhouchong, Han Jun, Zheng Yijie, Yang Tian

机构信息

Department of Hepatic Surgery, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, 200438, China.

Department of Clinical Laboratory, Peking University First Hospital, Beijing, China.

出版信息

Tumour Biol. 2016 Dec;37:15447–15456. doi: 10.1007/s13277-016-5443-x. Epub 2016 Oct 13.

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.

摘要

肝细胞癌(HCC)是全球癌症死亡的第三大主要原因。早期诊断可改善预后。维生素K拮抗剂-II诱导蛋白(PIVKA-II)是用于HCC诊断和预后的一种有效的血清生物标志物。与另一种血清生物标志物甲胎蛋白(AFP)联合使用时,HCC诊断的敏感性和特异性可分别提高至最高94%和98.5%。单独使用PIVKA-II或与AFP和/或AFP-L3联合使用,在预测根治性肝切除、化疗、靶向治疗、放疗及肝移植的治疗反应和临床结局方面均有效。日本临床指南推荐联合使用PIVKA-II和AFP用于HCC诊断、高危人群管理及抗癌治疗的预后评估。此外,PIVKA-II作为一个功能靶点,通过激活c-Met及其他信号转导通路促进HCC细胞的增殖、侵袭和转移。抑制PIVKA-II可能为HCC提供一种选择性且有效的治疗方法。

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