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使用甲胎蛋白高敏感岩藻糖基化组分早期检测肝细胞癌复发

Early Detection of Hepatocellular Carcinoma Recurrence Using the Highly Sensitive Fucosylated Fraction of Alpha-Fetoprotein.

作者信息

Setsu Toru, Tsuchiya Atsunori, Watanabe Takayuki, Nagoya Takuro, Ikarashi Satoshi, Hayashi Kazunao, Yokoyama Junji, Yamagiwa Satoshi, Terai Shuji

机构信息

Division of Gastroenterology and Hepatology, Graduate School of Medical and Dental Science, Niigata University, Niigata, Japan.

出版信息

Case Rep Gastroenterol. 2017 Mar 21;11(1):142-147. doi: 10.1159/000462969. eCollection 2017 Jan-Apr.

DOI:10.1159/000462969
PMID:28611567
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5465790/
Abstract

Alpha-fetoprotein (AFP)-L3 was originally reported as a hepatocellular carcinoma (HCC)-specific tumor marker, and recent accumulation of evidence has revealed that AFP-L3 frequency predicts the biological malignancy potential of HCC. However, AFP-L3 elevation from undetectable levels after curative treatment could not be discussed due to the difficulties of calculating AFP-L3 concentrations when serum AFP levels were low. Here, as a novel method, we used highly sensitive AFP-L3 frequency to predict HCC recurrence after curative treatment. Our cases illustrate that recognizing elevation of AFP-L3 from undetectable levels led to the early detection of recurrent HCC due to more careful surveillance.

摘要

甲胎蛋白异质体(AFP-L3)最初被报道为肝细胞癌(HCC)特异性肿瘤标志物,最近越来越多的证据表明,AFP-L3频率可预测HCC的生物学恶性潜能。然而,由于血清AFP水平较低时计算AFP-L3浓度存在困难,因此无法讨论根治性治疗后AFP-L3从不可检测水平升高的情况。在此,作为一种新方法,我们使用高灵敏度AFP-L3频率来预测根治性治疗后HCC的复发。我们的病例表明,由于更仔细的监测,识别AFP-L3从不可检测水平升高可导致复发性HCC的早期检测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2cf/5465790/7773fd1f541e/crg-0011-0142-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2cf/5465790/1923f1aead96/crg-0011-0142-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2cf/5465790/7773fd1f541e/crg-0011-0142-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2cf/5465790/1923f1aead96/crg-0011-0142-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2cf/5465790/7773fd1f541e/crg-0011-0142-g02.jpg

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本文引用的文献

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J Hepatol. 2016 Nov;65(5):888-898. doi: 10.1016/j.jhep.2016.05.022. Epub 2016 May 26.
2
Value of highly sensitive fucosylated fraction of alpha-fetoprotein for prediction of hepatocellular carcinoma recurrence after curative treatment.甲胎蛋白中高灵敏度岩藻糖基化片段对预测根治性治疗后肝细胞癌复发的价值。
Dig Dis Sci. 2013 Aug;58(8):2406-12. doi: 10.1007/s10620-013-2661-6. Epub 2013 Apr 18.
3
基于 LCA 磁阳离子聚合物脂质体的血清甲胎蛋白 L3 变体自动时间分辨荧光免疫分析提高肝癌诊断准确性。
Int J Nanomedicine. 2020 Jul 10;15:4933-4941. doi: 10.2147/IJN.S242527. eCollection 2020.
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Novel biomarkers for the management of chronic hepatitis B.用于慢性乙型肝炎管理的新型生物标志物。
Clin Mol Hepatol. 2020 Jul;26(3):261-279. doi: 10.3350/cmh.2020.0032. Epub 2020 Jun 15.
5
Diverse perspectives to address for the future treatment of heterogeneous hepatocellular carcinoma.应对异质性肝细胞癌未来治疗的多种观点。
Heliyon. 2019 Mar 11;5(3):e01325. doi: 10.1016/j.heliyon.2019.e01325. eCollection 2019 Mar.
6
Clinical outcome of hepatocellular carcinoma can be predicted by the expression of hepatic progenitor cell markers and serum tumour markers.肝细胞癌的临床结局可通过肝祖细胞标志物的表达和血清肿瘤标志物来预测。
Oncotarget. 2018 Apr 24;9(31):21844-21860. doi: 10.18632/oncotarget.25074.
Prognostic significance of a combination of pre- and post-treatment tumor markers for hepatocellular carcinoma curatively treated with hepatectomy.
术前和术后肿瘤标志物联合对肝癌根治性切除术后的预后意义。
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Dig Dis Sci. 2010 Jul;55(7):2095-101. doi: 10.1007/s10620-009-0954-6.