A possible role of microRNAs as predictive markers for the recurrence of hepatocellular carcinoma after liver transplantation

被引:37
|
作者
Liese, Juliane [1 ]
Peveling-Oberhag, Jan [2 ]
Doering, Claudia [3 ]
Schnitzbauer, Andreas A. [1 ]
Herrmann, Eva [4 ]
Zangos, Stephan [5 ]
Hansmann, Martin L. [3 ]
Moench, Christian [6 ]
Welker, Martin W. [2 ]
Zeuzem, Stefan [2 ]
Bechstein, Wolf O. [1 ]
Ulrich, Frank [1 ,7 ]
机构
[1] Goethe Univ Frankfurt, Univ Hosp Frankfurt, Dept Gen & Visceral Surg, Theodor Stern Kai 7, D-60590 Frankfurt, Germany
[2] Goethe Univ Frankfurt, Univ Hosp Frankfurt, Dept Internal Med 1, Theodor Stern Kai 7, D-60590 Frankfurt, Germany
[3] Goethe Univ Frankfurt, Univ Hosp Frankfurt, Dr Senckenberg Inst Pathol, Theodor Stern Kai 7, D-60590 Frankfurt, Germany
[4] Goethe Univ Frankfurt, Univ Hosp Frankfurt, Inst Biostat & Math Modelling, Theodor Stern Kai 7, D-60590 Frankfurt, Germany
[5] Goethe Univ Frankfurt, Univ Hosp Frankfurt, Ctr Radiol, Theodor Stern Kai 7, D-60590 Frankfurt, Germany
[6] Westpfalz Klinikum, Gen Visceral & Transplantat Surg, Kaiserslautern, Germany
[7] Klinikum Wetzlar, Gen & Visceral Surg, Wetzlar, Germany
关键词
biomarker; hepatocellular carcinoma; liver transplantation; microRNA; tumour recurrence; DOWN-REGULATION; GROWTH-FACTOR; TUMOR-SUPPRESSOR; SURVIVAL; CANCER; EXPRESSION; CIRRHOSIS; GENES; MILAN;
D O I
10.1111/tri.12733
中图分类号
R61 [外科手术学];
学科分类号
摘要
With favourable 5-year survival rates up to 75%, liver transplantation (LT) is the treatment of choice for hepatocellular carcinoma (HCC). Nonetheless, tumour recurrence after LT remains a challenge. The aim of this retrospective study was to develop a predictive score for tumour recurrence after LT by combining clinical parameters with HCC biomarkers (microRNA). A microRNA (miRNA) microarray analysis was used to compare miRNA expression patterns in tissue samples of 40 patients with and without HCC recurrence after LT. In a screening cohort (n = 18), the miRNA analysis identified significant differences in the expression of 13 miRNAs in patients with tumour recurrence. Using the most significant miRNAs in this screening cohort, we could develop a predictive score, which combined the expression levels of miR-214, miR-3187 and the Milan criteria, and we could define low- and high-risk groups for tumour recurrence and death. The above score was evaluated in a second and independent cohort (n = 22). In contrast to the Milan criteria alone, this score was significantly associated with tumour recurrence. Our analysis indicated that the use of a specific miRNA expression pattern in combination with a limited tumour burden as defined by the Milan criteria may lead to a more accurate prediction of tumour recurrence.
引用
收藏
页码:369 / 380
页数:12
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