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尸检时的血浆游离细胞 DNA 测序:“液体解剖”的概念验证研究。

Post-mortem Plasma Cell-Free DNA Sequencing: Proof-of-Concept Study for the "Liquid Autopsy".

机构信息

Department of Cancer Genome Informatics, Graduate School of Medicine, Osaka University, Osaka, Japan.

Department of Clinical Genomics, Graduate School of Medicine, Osaka University, Osaka, Japan.

出版信息

Sci Rep. 2020 Feb 7;10(1):2120. doi: 10.1038/s41598-020-59193-y.

Abstract

Recent genomic studies on cancer tissues obtained during rapid autopsy have provided insights into the clonal evolution and heterogeneity of cancer. However, post-mortem blood has not been subjected to genetic analyses in relation to cancer. We first confirmed that substantial quantities of cell-free DNA were present in the post-mortem plasma of 12 autopsy cases. Then, we focused on a pilot case of prostate cancer with multiple metastases for genetic analyses. Whole-exome sequencing of post-mortem plasma-derived cell-free DNA and eight frozen metastatic cancer tissues collected during rapid autopsy was performed, and compared their mutational statuses. The post-mortem plasma cell-free DNA was successfully sequenced and 344 mutations were identified. Of these, 160 were detected in at least one of the metastases. Further, 99% of the mutations shared by all metastases were present in the plasma. Sanger sequencing of 30 additional formalin-fixed metastases enabled us to map the clones harboring mutations initially detected only in the plasma. In conclusion, post-mortem blood, which is usually disposed of during conventional autopsies, can provide valuable data if sequenced in detail, especially regarding cancer heterogeneity. Furthermore, post-mortem plasma cell-free DNA sequencing (liquid autopsy) can be a novel platform for cancer research and a tool for genomic pathology.

摘要

最近在快速尸检时对癌症组织进行的基因组研究,为癌症的克隆进化和异质性提供了一些见解。然而,死后血液尚未进行与癌症相关的遗传分析。我们首先证实,在 12 例尸检的死后血浆中存在大量的游离细胞 DNA。然后,我们专注于一例具有多个转移的前列腺癌进行遗传分析。对死后血浆衍生的游离 DNA 和在快速尸检时收集的 8 个冷冻转移性癌症组织进行了全外显子组测序,并比较了它们的突变状态。成功地对死后血浆游离 DNA 进行了测序,鉴定出 344 个突变。其中,至少在一个转移灶中检测到 160 个突变。此外,所有转移灶共有的 99%的突变都存在于血浆中。对另外 30 个福尔马林固定转移灶进行 Sanger 测序,使我们能够绘制最初仅在血浆中检测到的突变所携带的克隆图谱。总之,如果详细测序,通常在常规尸检中丢弃的死后血液可以提供有价值的数据,特别是在癌症异质性方面。此外,死后血浆游离 DNA 测序(液体尸检)可以成为癌症研究的新平台和基因组病理学的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71ce/7005783/2b175d108fa8/41598_2020_59193_Fig1_HTML.jpg

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