Abstract

High-grade dysplasia carries significant risk of transformation to hepatocellular carcinoma (HCC). Despite this, at the current standard of care, all non-malignant hepatic nodules including high-grade dysplastic nodules are managed similarly. This is partly related to difficulties in distinguishing high-risk pathology in the liver. We aimed to identify chromosome arm-level somatic copy number alterations (SCNAs) that characterise the transition of liver nodules along the cirrhosis-dysplasia-carcinoma axis. We validated our findings on an independent cohort using blood-derived cell-free DNA. A repository of non-cancer DNA sequences obtained from patients with HCC (n = 389) was analysed to generate cut-off thresholds aiming to minimise false-positive SCNAs. Tissue samples representing stages from the multistep process of hepatocarcinogenesis (n = 184) were subjected to low-pass whole genome sequencing. Chromosome arm-level SCNAs were identified in liver cirrhosis, dysplastic nodules, and HCC to assess their discriminative capacity. Samples positive for 1q+ or 8q+ arm-level duplications were likely to be either HCC or high-grade dysplastic nodules as opposed to low-grade dysplastic nodules or cirrhotic tissue with an odds ratio (OR) of 35.5 (95% CI 11.5-110) and 16 (95% CI 6.4-40.2), respectively (p < 0.0001). In an independent cohort of patients recruited from Nottingham, UK, at least two out of four alterations (1q+, 4q-, 8p-, and 8q+) were detectable in blood-derived cell-free DNA of patients with HCC (n = 22) but none of the control patients with liver cirrhosis (n = 9). Arm-level SCNAs on 1q+ or 8q+ are associated with high-risk liver pathology. These can be detected using low-pass sequencing of cell-free DNA isolated from blood, which may be a future early cancer screening tool for patients with liver cirrhosis. © 2021 The Authors. The Journal of Pathology published by John Wiley & Sons, Ltd. on behalf of The Pathological Society of Great Britain and Ireland.

Highlights

  • Events in hepatocarcinogenesis involve the progression of dysplastic nodules (DNs) to overt hepatocellular carcinoma (HCC)

  • Genomic features common to hepatic dysplasia and carcinoma demonstrate a step-wise increase in chromosome arm-level somatic copy number alterations (SCNAs) [3,4], chromosomal instability [3,5], and TERT promoter mutations [6,7]

  • To identify the potential for arm-level SCNAs in aiding the discrimination of well-differentiated HCC from high-grade DNs, we examined the prevalence of key arm-level SCNAs within both groups

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Summary

Introduction

Events in hepatocarcinogenesis involve the progression of dysplastic nodules (DNs) to overt hepatocellular carcinoma (HCC). Such a contention has been supported by the frequent appearance of nodule-innodule lesions containing both dysplasia and cancer [1]. In comparison to regenerative nodules, DNs have an increased risk of malignant transformation [2]. A histological distinction can be drawn between those that are ‘low-grade’ DNs and those that are ‘high-grade’. The latter are assumed to be the immediate precursors of overt HCC. The rate of HCC development was found to be significantly higher in high-grade DNs than in low-grade DNs and regenerative nodules [8]

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