• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

克隆性造血突变的全面景观和干扰:中国泛癌队列。

Comprehensive landscape and interference of clonal haematopoiesis mutations for liquid biopsy: A Chinese pan-cancer cohort.

机构信息

The First School of Clinical Medicine, Southern Medical University, Guangzhou, China.

Department of Thoracic Surgery, General Hospital of Southern Theater Command, PLA, Guangzhou, China.

出版信息

J Cell Mol Med. 2021 Nov;25(21):10279-10290. doi: 10.1111/jcmm.16966. Epub 2021 Oct 17.

DOI:10.1111/jcmm.16966
PMID:34658138
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8572768/
Abstract

Tumour-derived DNA found in the plasma of cancer patients provides the probability to detect somatic mutations from circulating cell-free DNA (cfDNA) in plasma samples. However, clonal hematopoiesis (CH) mutations affect the accuracy of liquid biopsy for cancer diagnosis and treatment. Here, we integrated landscape of CH mutations in 11,725 pan-cancer patients of Chinese and explored effects of CH on liquid biopsies in real-world. We first identified 5933 CHs based on panel sequencing of matched DNA of white blood cell and cfDNA on 301 genes for 5100 patients, in which CH number of patients had positive correlation with their diagnosis age. We observed that canonical genes related to CH, including DNMT3A, TET2, ASXL1, TP53, ATM, CHEK2 and SF3B1, were dominant in the Chinese cohort and 13.29% of CH mutations only appeared in the Chinese cohort compared with the Western cohort. Analysis of CH gene distribution bias indicated that CH tended to appear in genes with functions of tyrosine kinase regulation, PI3K-Akt signalling and TP53 activity, suggesting unfavourable effects of CH mutations in cancer patients. We further confirmed effect of driver genes carried by CH on somatic mutations in liquid biopsy of cancer patients. Forty-eight actionable somatic mutations in 17 driver genes were considered CH genes in 92 patients (1.80%) of the Chinese cohort, implying potential impacts of CH on clinical decision-making. Taken together, this study exhibits strong evidence that gene mutations from CH interfere accuracy of liquid biopsies using cfDNA in cancer diagnosis and treatment in real-world.

摘要

肿瘤来源的 DNA 存在于癌症患者的血浆中,为检测血浆样本中循环无细胞 DNA (cfDNA) 的体细胞突变提供了可能性。然而,克隆性造血 (CH) 突变会影响液体活检在癌症诊断和治疗中的准确性。在这里,我们整合了中国 11725 例泛癌症患者的 CH 突变图谱,并在真实世界中探索了 CH 对液体活检的影响。我们首先基于 301 个基因的白细胞 DNA 和 cfDNA 的匹配 DNA 面板测序,在 5100 例患者中鉴定了 5933 个 CH,其中患者的 CH 数量与他们的诊断年龄呈正相关。我们观察到,与 CH 相关的典型基因,包括 DNMT3A、TET2、ASXL1、TP53、ATM、CHEK2 和 SF3B1,在中国队列中占主导地位,而 13.29%的 CH 突变仅在中国队列中出现,而在西方队列中没有。CH 基因分布偏差分析表明,CH 倾向于出现在与酪氨酸激酶调节、PI3K-Akt 信号和 TP53 活性相关的基因中,提示 CH 突变对癌症患者有不利影响。我们进一步证实了 CH 携带的驱动基因对癌症患者液体活检中体细胞突变的影响。在 92 例中国队列患者 (1.80%)中,有 17 个驱动基因携带 48 个可操作的体细胞突变被认为是 CH 基因,这意味着 CH 对临床决策有潜在影响。总之,这项研究有力地表明,来自 CH 的基因突变会干扰液体活检在癌症诊断和治疗中的准确性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/908c/8572768/c7825311abed/JCMM-25-10279-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/908c/8572768/cb0097ee5402/JCMM-25-10279-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/908c/8572768/63b30da2e0ef/JCMM-25-10279-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/908c/8572768/c543a26e6cf8/JCMM-25-10279-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/908c/8572768/15e1805b9ef9/JCMM-25-10279-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/908c/8572768/c7825311abed/JCMM-25-10279-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/908c/8572768/cb0097ee5402/JCMM-25-10279-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/908c/8572768/63b30da2e0ef/JCMM-25-10279-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/908c/8572768/c543a26e6cf8/JCMM-25-10279-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/908c/8572768/15e1805b9ef9/JCMM-25-10279-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/908c/8572768/c7825311abed/JCMM-25-10279-g002.jpg

相似文献

1
Comprehensive landscape and interference of clonal haematopoiesis mutations for liquid biopsy: A Chinese pan-cancer cohort.克隆性造血突变的全面景观和干扰:中国泛癌队列。
J Cell Mol Med. 2021 Nov;25(21):10279-10290. doi: 10.1111/jcmm.16966. Epub 2021 Oct 17.
2
Clinical significance of clonal hematopoiesis in the interpretation of blood liquid biopsy.克隆性造血在液体活检解读中的临床意义。
Mol Oncol. 2020 Aug;14(8):1719-1730. doi: 10.1002/1878-0261.12727. Epub 2020 Jun 8.
3
High prevalence of clonal hematopoiesis-type genomic abnormalities in cell-free DNA in invasive gliomas after treatment.治疗后侵袭性神经胶质瘤的游离 DNA 中存在高频率的克隆性造血基因组异常。
Int J Cancer. 2021 Jun 1;148(11):2839-2847. doi: 10.1002/ijc.33481. Epub 2021 Feb 5.
4
Chemotherapy-associated clonal hematopoiesis mutations should be taken seriously in plasma cell-free DNA KRAS/NRAS/BRAF genotyping for metastatic colorectal cancer.在对转移性结直肠癌进行血浆无细胞 DNA KRAS/NRAS/BRAF 基因分型时,应认真对待化疗相关的克隆性造血突变。
Clin Biochem. 2021 Jun;92:46-53. doi: 10.1016/j.clinbiochem.2021.03.005. Epub 2021 Mar 15.
5
Clinical relevance of clonal hematopoiesis and its interference in cell-free DNA profiling of patients with gastric cancer.克隆性造血及其对胃癌患者游离 DNA 谱分析干扰的临床相关性。
Clin Chem Lab Med. 2023 Jul 13;62(1):178-186. doi: 10.1515/cclm-2023-0261. Print 2024 Jan 26.
6
Identification of Clonal Hematopoiesis Mutations in Solid Tumor Patients Undergoing Unpaired Next-Generation Sequencing Assays.实体瘤患者在接受非配对下一代测序检测时的克隆性造血基因突变的鉴定。
Clin Cancer Res. 2018 Dec 1;24(23):5918-5924. doi: 10.1158/1078-0432.CCR-18-1201. Epub 2018 Jun 4.
7
Clonal haematopoiesis in chronic ischaemic heart failure: prognostic role of clone size for DNMT3A- and TET2-driver gene mutations.慢性缺血性心力衰竭中的克隆性造血:DNMT3A 和 TET2 驱动基因突变的克隆大小对预后的作用。
Eur Heart J. 2021 Jan 20;42(3):257-265. doi: 10.1093/eurheartj/ehaa845.
8
Clonal hematopoiesis detection in patients with cancer using cell-free DNA sequencing.使用游离细胞 DNA 测序检测癌症患者的克隆性造血。
Sci Transl Med. 2023 Mar 29;15(689):eabm8729. doi: 10.1126/scitranslmed.abm8729.
9
Review of clonal hematopoiesis, subtypes and its role in neoplasia and different morbidities.克隆性造血的综述、亚型及其在肿瘤形成和不同疾病中的作用。
Leuk Res. 2023 Jul;130:107307. doi: 10.1016/j.leukres.2023.107307. Epub 2023 May 5.
10
Tumor fraction-guided cell-free DNA profiling in metastatic solid tumor patients.肿瘤分数指导下的转移性实体瘤患者游离 DNA 分析。
Genome Med. 2021 May 31;13(1):96. doi: 10.1186/s13073-021-00898-8.

引用本文的文献

1
Clonal Hematopoiesis and Solid Cancers.克隆性造血与实体癌
Cancer Sci. 2025 Aug;116(8):2055-2063. doi: 10.1111/cas.70097. Epub 2025 May 19.
2
Predicting somatic mutation origins in cell-free DNA by semi-supervised GAN models.利用半监督生成对抗网络模型预测游离DNA中的体细胞突变起源
Heliyon. 2024 Oct 15;10(20):e39379. doi: 10.1016/j.heliyon.2024.e39379. eCollection 2024 Oct 30.
3
Distinct landscape and clinical implications of therapy-related clonal hematopoiesis.治疗相关的克隆性造血的独特景观和临床意义。

本文引用的文献

1
Comprehensive next-generation profiling of clonal hematopoiesis in cancer patients using paired tumor-blood sequencing for guiding personalized therapies.利用配对肿瘤-血液测序对癌症患者的克隆造血进行全面的下一代分析,以指导个性化治疗。
Clin Transl Med. 2020 Nov;10(7):e222. doi: 10.1002/ctm2.222.
2
Association of Clonal Hematopoiesis in DNA Repair Genes With Prostate Cancer Plasma Cell-free DNA Testing Interference.DNA 修复基因中克隆性造血与前列腺癌无细胞血浆 DNA 检测干扰的关联。
JAMA Oncol. 2021 Jan 1;7(1):107-110. doi: 10.1001/jamaoncol.2020.5161.
3
Cancer therapy shapes the fitness landscape of clonal hematopoiesis.
J Clin Invest. 2024 Oct 1;134(19):e180069. doi: 10.1172/JCI180069.
4
Clinical utility of BRCA and ATM mutation status in circulating tumour DNA for treatment selection in advanced pancreatic cancer.BRCA 和 ATM 突变状态在循环肿瘤 DNA 中对晚期胰腺癌治疗选择的临床效用。
Br J Cancer. 2024 Oct;131(7):1237-1245. doi: 10.1038/s41416-024-02834-0. Epub 2024 Aug 28.
5
Identification of gene variation feature for targeted therapy of non-small cell lung cancer through combined method of DNA and RNA sequencing.通过DNA和RNA测序联合方法鉴定非小细胞肺癌靶向治疗的基因变异特征
Discov Oncol. 2024 Mar 6;15(1):67. doi: 10.1007/s12672-024-00915-3.
6
Mutational landscape of pan-cancer patients with PIK3CA alterations in Chinese population.中国人群中 PIK3CA 改变的泛癌症患者的突变特征。
BMC Med Genomics. 2022 Jul 1;15(1):146. doi: 10.1186/s12920-022-01297-7.
癌症治疗改变了克隆性造血的适应性景观。
Nat Genet. 2020 Nov;52(11):1219-1226. doi: 10.1038/s41588-020-00710-0. Epub 2020 Oct 26.
4
Non-invasive early detection of cancer four years before conventional diagnosis using a blood test.利用血液检测,可在常规诊断前四年进行非侵入性的癌症早期检测。
Nat Commun. 2020 Jul 21;11(1):3475. doi: 10.1038/s41467-020-17316-z.
5
The mutational constraint spectrum quantified from variation in 141,456 humans.从 141456 名人类个体的变异中量化的突变约束谱。
Nature. 2020 May;581(7809):434-443. doi: 10.1038/s41586-020-2308-7. Epub 2020 May 27.
6
Clonal hematopoiesis: background player in plasma cell-free DNA variants.克隆性造血:游离DNA变体中的幕后参与者
Ann Transl Med. 2019 Dec;7(Suppl 8):S384. doi: 10.21037/atm.2019.12.97.
7
High-intensity sequencing reveals the sources of plasma circulating cell-free DNA variants.高通量测序揭示了血浆游离循环 DNA 变异体的来源。
Nat Med. 2019 Dec;25(12):1928-1937. doi: 10.1038/s41591-019-0652-7. Epub 2019 Nov 25.
8
The reactome pathway knowledgebase.Reactome 通路知识库。
Nucleic Acids Res. 2020 Jan 8;48(D1):D498-D503. doi: 10.1093/nar/gkz1031.
9
The ENCODE Blacklist: Identification of Problematic Regions of the Genome.ENCODE 黑名单:基因组中问题区域的鉴定。
Sci Rep. 2019 Jun 27;9(1):9354. doi: 10.1038/s41598-019-45839-z.
10
Liquid biopsy and minimal residual disease - latest advances and implications for cure.液体活检与微小残留病灶——最新进展及其对治愈的影响。
Nat Rev Clin Oncol. 2019 Jul;16(7):409-424. doi: 10.1038/s41571-019-0187-3.