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评估 cfDNA 作为致密组织乳腺癌的早期检测方法。

Evaluation of cfDNA as an early detection assay for dense tissue breast cancer.

机构信息

Department of Health Management and Informatics, Center for Biomedical Informatics, School of Medicine, University of Missouri, 1 Hospital Drive, MA213, Columbia, MO, 65212, USA.

Medical School of Tunis, University of Tunis El Manar, Tunis, Tunisia.

出版信息

Sci Rep. 2022 May 19;12(1):8458. doi: 10.1038/s41598-022-12457-1.

Abstract

A cell-free DNA (cfDNA) assay would be a promising approach to early cancer diagnosis, especially for patients with dense tissues. Consistent cfDNA signatures have been observed for many carcinogens. Recently, investigations of cfDNA as a reliable early detection bioassay have presented a powerful opportunity for detecting dense tissue screening complications early. We performed a prospective study to evaluate the potential of characterizing cfDNA as a central element in the early detection of dense tissue breast cancer (BC). Plasma samples were collected from 32 consenting subjects with dense tissue and positive mammograms, 20 with positive biopsies and 12 with negative biopsies. After screening and before biopsy, cfDNA was extracted, and whole-genome next-generation sequencing (NGS) was performed on all samples. Copy number alteration (CNA) and single nucleotide polymorphism (SNP)/insertion/deletion (Indel) analyses were performed to characterize cfDNA. In the positive-positive subjects (cases), a total of 5 CNAs overlapped with 5 previously reported BC-related oncogenes (KSR2, MAP2K4, MSI2, CANT1 and MSI2). In addition, 1 SNP was detected in KMT2C, a BC oncogene, and 9 others were detected in or near 10 genes (SERAC1, DAGLB, MACF1, NVL, FBXW4, FANK1, KCTD4, CAVIN1; ATP6V0A1 and ZBTB20-AS1) previously associated with non-BC cancers. For the positive-negative subjects (screening), 3 CNAs were detected in BC genes (ACVR2A, CUL3 and PIK3R1), and 5 SNPs were identified in 6 non-BC cancer genes (SNIP1, TBC1D10B, PANK1, PRKCA and RUNX2; SUPT3H). This study presents evidence of the potential of using cfDNA somatic variants as dense tissue BC biomarkers from a noninvasive liquid bioassay for early cancer detection.

摘要

无细胞游离 DNA (cfDNA) 检测可能是癌症早期诊断的一种很有前途的方法,特别是对于组织致密的患者。许多致癌物质都观察到了一致的 cfDNA 特征。最近,将 cfDNA 作为可靠的早期检测生物标志物的研究为早期发现致密组织筛查并发症提供了有力的机会。我们进行了一项前瞻性研究,以评估将 cfDNA 作为致密组织乳腺癌 (BC) 早期检测的核心要素的潜力。从 32 名同意参加的致密组织和阳性乳房 X 光片的受试者、20 名阳性活检和 12 名阴性活检的受试者中采集血浆样本。在筛选和活检之前,提取 cfDNA,并对所有样本进行全基因组下一代测序 (NGS)。进行拷贝数改变 (CNA) 和单核苷酸多态性 (SNP)/插入/缺失 (Indel) 分析以表征 cfDNA。在阳性阳性受试者(病例)中,总共检测到 5 个与 5 个先前报道的 BC 相关致癌基因 (KSR2、MAP2K4、MSI2、CANT1 和 MSI2) 重叠的 CNA。此外,在 BC 致癌基因 KMT2C 中检测到 1 个 SNP,在 10 个基因(SERAC1、DAGLB、MACF1、NVL、FBXW4、FANK1、KCTD4、CAVIN1;ATP6V0A1 和 ZBTB20-AS1)中检测到 9 个其他 SNP 或附近与非 BC 癌症相关的基因。对于阳性阴性受试者(筛查),在 BC 基因(ACVR2A、CUL3 和 PIK3R1)中检测到 3 个 CNA,在 6 个非 BC 癌症基因(SNIP1、TBC1D10B、PANK1、PRKCA 和 RUNX2;SUPT3H)中检测到 5 个 SNP。这项研究提供了证据,表明使用 cfDNA 体细胞变异作为非侵入性液体生物标志物来检测早期癌症的致密组织 BC 生物标志物具有潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e226/9120463/7490e29483b3/41598_2022_12457_Fig1_HTML.jpg

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