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Whole-genome sequencing reveals the evolutionary trajectory of HBV-related hepatocellular carcinoma early recurrence

Patients with hepatocellular carcinoma (HCC) have poor long-term survival following curative resection because of the high rate of tumor early recurrence. Little is known about the trajectory of genomic evolution from primary to early-recurrent HCC. In this study, we performed whole-genome sequencin...

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Autores principales: Zhou, Shao-Lai, Zhou, Zheng-Jun, Song, Cheng-Li, Xin, Hao-Yang, Hu, Zhi-Qiang, Luo, Chu-Bin, Luo, Yi-Jie, Li, Jia, Dai, Zhi, Yang, Xin-Rong, Shi, Ying-Hong, Wang, Zheng, Huang, Xiao-Wu, Fan, Jia, Zhou, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789859/
https://www.ncbi.nlm.nih.gov/pubmed/35078970
http://dx.doi.org/10.1038/s41392-021-00838-3
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author Zhou, Shao-Lai
Zhou, Zheng-Jun
Song, Cheng-Li
Xin, Hao-Yang
Hu, Zhi-Qiang
Luo, Chu-Bin
Luo, Yi-Jie
Li, Jia
Dai, Zhi
Yang, Xin-Rong
Shi, Ying-Hong
Wang, Zheng
Huang, Xiao-Wu
Fan, Jia
Zhou, Jian
author_facet Zhou, Shao-Lai
Zhou, Zheng-Jun
Song, Cheng-Li
Xin, Hao-Yang
Hu, Zhi-Qiang
Luo, Chu-Bin
Luo, Yi-Jie
Li, Jia
Dai, Zhi
Yang, Xin-Rong
Shi, Ying-Hong
Wang, Zheng
Huang, Xiao-Wu
Fan, Jia
Zhou, Jian
author_sort Zhou, Shao-Lai
collection PubMed
description Patients with hepatocellular carcinoma (HCC) have poor long-term survival following curative resection because of the high rate of tumor early recurrence. Little is known about the trajectory of genomic evolution from primary to early-recurrent HCC. In this study, we performed whole-genome sequencing (WGS) on 40 pairs of primary and early-recurrent hepatitis B virus (HBV)-related HCC tumors from patients who received curative resection, and from four patients whose primary and recurrent tumor were extensively sampled. We identified two recurrence patterns: de novo recurrence (18/40), which developed genetically independently of the primary tumor and carried different HCC drivers, and ancestral recurrence (22/40), which was clonally related to the primary tumor and progressed more rapidly than de novo recurrence. We found that the recurrence location was predictive of the recurrence pattern: distant recurrence tended to display the de novo pattern, whereas local recurrence tended to display the ancestral pattern. We then uncovered the evolutionary trajectories based on the subclonal architecture, driver-gene mutations, and mutational processes observed in the primary and recurrent tumors. Multi-region WGS demonstrated spatiotemporal heterogeneity and polyclonal, monophyletic dissemination in HCC ancestral recurrence. In addition, we identified recurrence-specific mutations and copy-number gains in BCL9, leading to WNT/β-catenin signaling activation and an immune-excluded tumor microenvironment, which suggests that BCL9 might serve as a new therapeutic target for recurrent HCC. Collectively, our results allow us to view with unprecedented clarity the genomic evolution during HBV-related HCC early recurrence, providing an important molecular foundation for enhanced understanding of HCC with implications for personalized therapy to improve patient survival.
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spelling pubmed-87898592022-02-07 Whole-genome sequencing reveals the evolutionary trajectory of HBV-related hepatocellular carcinoma early recurrence Zhou, Shao-Lai Zhou, Zheng-Jun Song, Cheng-Li Xin, Hao-Yang Hu, Zhi-Qiang Luo, Chu-Bin Luo, Yi-Jie Li, Jia Dai, Zhi Yang, Xin-Rong Shi, Ying-Hong Wang, Zheng Huang, Xiao-Wu Fan, Jia Zhou, Jian Signal Transduct Target Ther Article Patients with hepatocellular carcinoma (HCC) have poor long-term survival following curative resection because of the high rate of tumor early recurrence. Little is known about the trajectory of genomic evolution from primary to early-recurrent HCC. In this study, we performed whole-genome sequencing (WGS) on 40 pairs of primary and early-recurrent hepatitis B virus (HBV)-related HCC tumors from patients who received curative resection, and from four patients whose primary and recurrent tumor were extensively sampled. We identified two recurrence patterns: de novo recurrence (18/40), which developed genetically independently of the primary tumor and carried different HCC drivers, and ancestral recurrence (22/40), which was clonally related to the primary tumor and progressed more rapidly than de novo recurrence. We found that the recurrence location was predictive of the recurrence pattern: distant recurrence tended to display the de novo pattern, whereas local recurrence tended to display the ancestral pattern. We then uncovered the evolutionary trajectories based on the subclonal architecture, driver-gene mutations, and mutational processes observed in the primary and recurrent tumors. Multi-region WGS demonstrated spatiotemporal heterogeneity and polyclonal, monophyletic dissemination in HCC ancestral recurrence. In addition, we identified recurrence-specific mutations and copy-number gains in BCL9, leading to WNT/β-catenin signaling activation and an immune-excluded tumor microenvironment, which suggests that BCL9 might serve as a new therapeutic target for recurrent HCC. Collectively, our results allow us to view with unprecedented clarity the genomic evolution during HBV-related HCC early recurrence, providing an important molecular foundation for enhanced understanding of HCC with implications for personalized therapy to improve patient survival. Nature Publishing Group UK 2022-01-26 /pmc/articles/PMC8789859/ /pubmed/35078970 http://dx.doi.org/10.1038/s41392-021-00838-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zhou, Shao-Lai
Zhou, Zheng-Jun
Song, Cheng-Li
Xin, Hao-Yang
Hu, Zhi-Qiang
Luo, Chu-Bin
Luo, Yi-Jie
Li, Jia
Dai, Zhi
Yang, Xin-Rong
Shi, Ying-Hong
Wang, Zheng
Huang, Xiao-Wu
Fan, Jia
Zhou, Jian
Whole-genome sequencing reveals the evolutionary trajectory of HBV-related hepatocellular carcinoma early recurrence
title Whole-genome sequencing reveals the evolutionary trajectory of HBV-related hepatocellular carcinoma early recurrence
title_full Whole-genome sequencing reveals the evolutionary trajectory of HBV-related hepatocellular carcinoma early recurrence
title_fullStr Whole-genome sequencing reveals the evolutionary trajectory of HBV-related hepatocellular carcinoma early recurrence
title_full_unstemmed Whole-genome sequencing reveals the evolutionary trajectory of HBV-related hepatocellular carcinoma early recurrence
title_short Whole-genome sequencing reveals the evolutionary trajectory of HBV-related hepatocellular carcinoma early recurrence
title_sort whole-genome sequencing reveals the evolutionary trajectory of hbv-related hepatocellular carcinoma early recurrence
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789859/
https://www.ncbi.nlm.nih.gov/pubmed/35078970
http://dx.doi.org/10.1038/s41392-021-00838-3
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