The First School of Clinical Medicine, Southern Medical University, Guangzhou, China.
Department of Thoracic Surgery, General Hospital of Southern Theater Command, PLA, Guangzhou, China.
J Cell Mol Med. 2021 Nov;25(21):10279-10290. doi: 10.1111/jcmm.16966. Epub 2021 Oct 17.
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.
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。