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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...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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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. |
format | Online Article Text |
id | pubmed-8789859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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