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从液体活检结果中鉴定循环肿瘤 DNA(ctDNA):一项观察性队列研究的结果。

Identification of circulating tumour DNA (ctDNA) from the liquid biopsy results: Findings from an observational cohort study.

机构信息

Centre for Advanced Medical Science and Technology, Tokyo Midtown Medical Center, Japan.

Centre for Advanced Medical Science and Technology, Tokyo Midtown Medical Center, Japan.

出版信息

Cancer Treat Res Commun. 2023;35:100701. doi: 10.1016/j.ctarc.2023.100701. Epub 2023 Apr 21.

Abstract

Liquid biopsies can be a rapid, cost-effective and non-invasive alternative to tumour biopsies for detecting genetic mutations in somatic tumours. Genetic profiling of liquid biopsies can also be used to identify novel antigens for targeted therapy, provide updated information on disease prognosis and evaluate treatment efficacy. In this study, we aimed to examine mutations that could be identified in liquid biopsy and their distribution in a small study cohort. We studied the genomic profiles of 99 blood samples from 85 patients with 21 different types of cancer using two commercially available liquid biopsy tests. The mean circulating free DNA (cfDNA) concentration was 162.7 ± 352.3 nanograms per 20 millilitres. Amongst cfDNA, the circulating tumour DNA (ctDNA) percentage ranged from 0.006% to 90.6%. With the exception of samples with gene amplification and high microsatellite instability, the number of mutations in each sample varied from zero to 21, with an average of 5.6 mutations in each patient. Amongst these mutations, nonsynonymous mutations were the most frequently observed type of mutation (90% of the sample, with an average frequency of 3.6 mutations per patient). Mutations were observed in 76 different genes. TP53 mutations constituted more than 16% of the detectable mutations, especially in non-small cell lung cancer. All the tumour types, except the ovary, kidney and apocrine gland tumours, harboured at least one type of TP53 mutation. KRAS (mainly in pancreatic cancer) and PIK3CA (mostly in breast cancer) mutations, were responsible for an additional 10% of the mutations in the studied samples. The tumour mutations were specific to each patient, as approximately 94.7% of the mutations were so unique that there was almost no duplication amongst the patients. These findings indicate that liquid biopsy can detect specific molecular changes of tumour, which is useful for precision oncology and personalized cancer treatment.

摘要

液体活检可以作为一种快速、经济有效的替代肿瘤活检的方法,用于检测体瘤中的基因突变。液体活检的基因谱分析也可用于鉴定新的抗原用于靶向治疗,提供疾病预后的最新信息,并评估治疗效果。在这项研究中,我们旨在研究液体活检中可以识别的突变及其在小研究队列中的分布。我们使用两种市售的液体活检检测方法研究了 85 名 21 种不同类型癌症患者的 99 份血液样本的基因组图谱。平均循环游离 DNA(cfDNA)浓度为每 20 毫升 162.7±352.3 纳克。在 cfDNA 中,循环肿瘤 DNA(ctDNA)的百分比范围为 0.006%至 90.6%。除了基因扩增和高微卫星不稳定性的样本外,每个样本的突变数量从 0 到 21 不等,每个患者的平均突变数量为 5.6 个。在这些突变中,非同义突变是最常见的突变类型(90%的样本,每个患者的平均频率为 3.6 个突变)。在 76 个不同的基因中观察到突变。TP53 突变构成了可检测突变的 16%以上,尤其是在非小细胞肺癌中。除了卵巢、肾脏和大汗腺肿瘤外,所有肿瘤类型都至少有一种 TP53 突变。KRAS(主要在胰腺癌中)和 PIK3CA(主要在乳腺癌中)突变导致研究样本中另外 10%的突变。肿瘤突变是每个患者特有的,因为大约 94.7%的突变是如此独特,以至于患者之间几乎没有重复。这些发现表明,液体活检可以检测肿瘤的特定分子变化,这对于精准肿瘤学和个体化癌症治疗是有用的。

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