Plasma DNA End-Motif Profiling as a Fragmentomic Marker in Cancer, Pregnancy, and Transplantation
Plasma DNA fragmentomics is an emerging area of research covering plasma DNA sizes, end points, and nucleosome footprints. In the present study, we found a significant increase in the diversity of plasma DNA end motifs in patients with hepatocellular carcinoma (HCC). Compared with patients without H...
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Published in | Cancer discovery Vol. 10; no. 5; pp. 664 - 673 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , |
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Language | English |
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01.05.2020
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Abstract | Plasma DNA fragmentomics is an emerging area of research covering plasma DNA sizes, end points, and nucleosome footprints. In the present study, we found a significant increase in the diversity of plasma DNA end motifs in patients with hepatocellular carcinoma (HCC). Compared with patients without HCC, patients with HCC showed a preferential pattern of 4-mer end motifs. In particular, the abundance of plasma DNA motif CCCA was much lower in patients with HCC than in subjects without HCC. The aberrant end motifs were also observed in patients with other cancer types, including colorectal cancer, lung cancer, nasopharyngeal carcinoma, and head and neck squamous cell carcinoma. We further observed that the profile of plasma DNA end motifs originating from the same organ, such as the liver, placenta, and hematopoietic cells, generally clustered together. The profile of end motifs may therefore serve as a class of biomarkers for liquid biopsy in oncology, noninvasive prenatal testing, and transplantation monitoring. SIGNIFICANCE: Plasma DNA molecules originating from the liver, HCC and other cancers, placenta, and hematopoietic cells each harbor a set of characteristic plasma DNA end motifs. Such markers carry tissue-of-origin information and represent a new class of biomarkers in the nascent field of fragmentomics.
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AbstractList | Plasma DNA fragmentomics is an emerging area of research covering plasma DNA sizes, end points, and nucleosome footprints. In the present study, we found a significant increase in the diversity of plasma DNA end motifs in patients with hepatocellular carcinoma (HCC). Compared with patients without HCC, patients with HCC showed a preferential pattern of 4-mer end motifs. In particular, the abundance of plasma DNA motif CCCA was much lower in patients with HCC than in subjects without HCC. The aberrant end motifs were also observed in patients with other cancer types, including colorectal cancer, lung cancer, nasopharyngeal carcinoma, and head and neck squamous cell carcinoma. We further observed that the profile of plasma DNA end motifs originating from the same organ, such as the liver, placenta, and hematopoietic cells, generally clustered together. The profile of end motifs may therefore serve as a class of biomarkers for liquid biopsy in oncology, noninvasive prenatal testing, and transplantation monitoring. SIGNIFICANCE: Plasma DNA molecules originating from the liver, HCC and other cancers, placenta, and hematopoietic cells each harbor a set of characteristic plasma DNA end motifs. Such markers carry tissue-of-origin information and represent a new class of biomarkers in the nascent field of fragmentomics.
. Plasma DNA fragmentomics is an emerging area of research covering plasma DNA sizes, end points, and nucleosome footprints. In the present study, we found a significant increase in the diversity of plasma DNA end motifs in patients with hepatocellular carcinoma (HCC). Compared with patients without HCC, patients with HCC showed a preferential pattern of 4-mer end motifs. In particular, the abundance of plasma DNA motif CCCA was much lower in patients with HCC than in subjects without HCC. The aberrant end motifs were also observed in patients with other cancer types, including colorectal cancer, lung cancer, nasopharyngeal carcinoma, and head and neck squamous cell carcinoma. We further observed that the profile of plasma DNA end motifs originating from the same organ, such as the liver, placenta, and hematopoietic cells, generally clustered together. The profile of end motifs may therefore serve as a class of biomarkers for liquid biopsy in oncology, noninvasive prenatal testing, and transplantation monitoring. SIGNIFICANCE: Plasma DNA molecules originating from the liver, HCC and other cancers, placenta, and hematopoietic cells each harbor a set of characteristic plasma DNA end motifs. Such markers carry tissue-of-origin information and represent a new class of biomarkers in the nascent field of fragmentomics.This article is highlighted in the In This Issue feature, p. 627.Plasma DNA fragmentomics is an emerging area of research covering plasma DNA sizes, end points, and nucleosome footprints. In the present study, we found a significant increase in the diversity of plasma DNA end motifs in patients with hepatocellular carcinoma (HCC). Compared with patients without HCC, patients with HCC showed a preferential pattern of 4-mer end motifs. In particular, the abundance of plasma DNA motif CCCA was much lower in patients with HCC than in subjects without HCC. The aberrant end motifs were also observed in patients with other cancer types, including colorectal cancer, lung cancer, nasopharyngeal carcinoma, and head and neck squamous cell carcinoma. We further observed that the profile of plasma DNA end motifs originating from the same organ, such as the liver, placenta, and hematopoietic cells, generally clustered together. The profile of end motifs may therefore serve as a class of biomarkers for liquid biopsy in oncology, noninvasive prenatal testing, and transplantation monitoring. SIGNIFICANCE: Plasma DNA molecules originating from the liver, HCC and other cancers, placenta, and hematopoietic cells each harbor a set of characteristic plasma DNA end motifs. Such markers carry tissue-of-origin information and represent a new class of biomarkers in the nascent field of fragmentomics.This article is highlighted in the In This Issue feature, p. 627. |
Author | Cheng, Suk Hang Heung, Macy M.S. Wong, Vincent W.S. Lo, Y.M. Dennis Ni, Meng Leung, Tak Yeung Lam, W.K. Jacky Yeung, Philip C. Chan, Jason Y.K. Chan, Rebecca W.Y. Sun, Kun Shang, Huimin Wong, John Chan, Henry L.Y. Xie, Tingting Zhou, Ze Chan, K.C. Allen Jiang, Peiyong Peng, Wenlei Poon, Liona C. Chiu, Rossa W.K. |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32111602$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1101/gr.242719.118 10.1126/scitranslmed.3007094 10.1016/j.cell.2015.11.050 10.1093/clinchem/48.3.421 10.1073/pnas.1814616115 10.1126/scitranslmed.3001720 10.1186/1471-2164-16-S13-S1 10.1073/pnas.1517494112 10.1126/scitranslmed.aat4921 10.1073/pnas.1815031116 10.1073/pnas.1615800113 10.1073/pnas.1313995110 10.1016/S0140-6736(97)02174-0 10.1373/clinchem.2011.169318 10.1373/clinchem.2016.254813 10.1373/clinchem.2003.024893 10.1073/pnas.1500076112 10.1186/gb-2010-11-10-r106 10.1016/j.ajhg.2020.01.008 10.1038/cr.2017.106 10.1016/S0140-6736(05)79055-3 10.1073/pnas.1508736112 10.1373/clinchem.2016.265702 10.1373/clinchem.2018.290304 |
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References | Song (2022060622181420700_bib18) 2017; 27 Sun (2022060622181420700_bib20) 2019; 29 Chan (2022060622181420700_bib7) 2003; 63 De Vlaminck (2022060622181420700_bib11) 2015; 112 Anders (2022060622181420700_bib17) 2010; 11 Jiang (2022060622181420700_bib5) 2018; 115 Zheng (2022060622181420700_bib10) 2012; 58 Yu (2022060622181420700_bib14) 2017; 63 Chan (2022060622181420700_bib1) 2004; 50 Gai (2022060622181420700_bib22) 2018; 64 Sun (2022060622181420700_bib12) 2015; 112 Han (2022060622181420700_bib25) 2020; 106 Chan (2022060622181420700_bib21) 2013; 110 Lo (2022060622181420700_bib8) 1998; 351 Serpas (2022060622181420700_bib16) 2019; 116 Jiang (2022060622181420700_bib24) 2017; 63 Bettegowda (2022060622181420700_bib19) 2014; 6 Ivanov (2022060622181420700_bib6) 2015; 16 Lo (2022060622181420700_bib23) 1997; 350 Jiang (2022060622181420700_bib13) 2015; 112 Mouliere (2022060622181420700_bib15) 2018; 10 Lo (2022060622181420700_bib2) 2010; 2 Snyder (2022060622181420700_bib3) 2016; 164 Lui (2022060622181420700_bib9) 2002; 48 Chan (2022060622181420700_bib4) 2016; 113 |
References_xml | – volume: 29 start-page: 418 year: 2019 ident: 2022060622181420700_bib20 article-title: Orientation-aware plasma cell-free DNA fragmentation analysis in open chromatin regions informs tissue of origin publication-title: Genome Res doi: 10.1101/gr.242719.118 – volume: 6 start-page: iii7 year: 2014 ident: 2022060622181420700_bib19 article-title: Detection of circulating tumor DNA in early- and late-stage human malignancies publication-title: Sci Transl Med doi: 10.1126/scitranslmed.3007094 – volume: 164 start-page: 57 year: 2016 ident: 2022060622181420700_bib3 article-title: Cell-free DNA comprises an in vivo nucleosome footprint that informs its tissues-of-origin publication-title: Cell doi: 10.1016/j.cell.2015.11.050 – volume: 48 start-page: 421 year: 2002 ident: 2022060622181420700_bib9 article-title: Predominant hematopoietic origin of cell-free dna in plasma and serum after sex-mismatched bone marrow transplantation publication-title: Clin Chem doi: 10.1093/clinchem/48.3.421 – volume: 115 start-page: E10925 year: 2018 ident: 2022060622181420700_bib5 article-title: Preferred end coordinates and somatic variants as signatures of circulating tumor DNA associated with hepatocellular carcinoma publication-title: Proc Natl Acad Sci U S A doi: 10.1073/pnas.1814616115 – volume: 63 start-page: 2028 year: 2003 ident: 2022060622181420700_bib7 article-title: Molecular characterization of circulating EBV DNA in the plasma of nasopharyngeal carcinoma and lymphoma patients publication-title: Cancer Res – volume: 2 start-page: 61ra91 year: 2010 ident: 2022060622181420700_bib2 article-title: Maternal plasma DNA sequencing reveals the genome-wide genetic and mutational profile of the fetus publication-title: Sci Transl Med doi: 10.1126/scitranslmed.3001720 – volume: 16 start-page: S1 year: 2015 ident: 2022060622181420700_bib6 article-title: Non-random fragmentation patterns in circulating cell-free DNA reflect epigenetic regulation publication-title: BMC Genomics doi: 10.1186/1471-2164-16-S13-S1 – volume: 112 start-page: 13336 year: 2015 ident: 2022060622181420700_bib11 article-title: Noninvasive monitoring of infection and rejection after lung transplantation publication-title: Proc Natl Acad Sci U S A doi: 10.1073/pnas.1517494112 – volume: 10 start-page: eaat4921 year: 2018 ident: 2022060622181420700_bib15 article-title: Enhanced detection of circulating tumor DNA by fragment size analysis publication-title: Sci Transl Med doi: 10.1126/scitranslmed.aat4921 – volume: 116 start-page: 641 year: 2019 ident: 2022060622181420700_bib16 article-title: Dnase1l3 deletion causes aberrations in length and end-motif frequencies in plasma DNA publication-title: Proc Natl Acad Sci U S A doi: 10.1073/pnas.1815031116 – volume: 113 start-page: E8159 year: 2016 ident: 2022060622181420700_bib4 article-title: Second generation noninvasive fetal genome analysis reveals de novo mutations, single-base parental inheritance, and preferred DNA ends publication-title: Proc Natl Acad Sci U S A doi: 10.1073/pnas.1615800113 – volume: 110 start-page: 18761 year: 2013 ident: 2022060622181420700_bib21 article-title: Noninvasive detection of cancer-associated genome-wide hypomethylation and copy number aberrations by plasma DNA bisulfite sequencing publication-title: Proc Natl Acad Sci U S A doi: 10.1073/pnas.1313995110 – volume: 350 start-page: 485 year: 1997 ident: 2022060622181420700_bib23 article-title: Presence of fetal DNA in maternal plasma and serum publication-title: Lancet doi: 10.1016/S0140-6736(97)02174-0 – volume: 58 start-page: 549 year: 2012 ident: 2022060622181420700_bib10 article-title: Nonhematopoietically derived DNA is shorter than hematopoietically derived DNA in plasma: a transplantation model publication-title: Clin Chem doi: 10.1373/clinchem.2011.169318 – volume: 63 start-page: 495 year: 2017 ident: 2022060622181420700_bib14 article-title: Combined count- and size-based analysis of maternal plasma DNA for noninvasive prenatal detection of fetal subchromosomal aberrations facilitates elucidation of the fetal and/or maternal origin of the aberrations publication-title: Clin Chem doi: 10.1373/clinchem.2016.254813 – volume: 50 start-page: 88 year: 2004 ident: 2022060622181420700_bib1 article-title: Size distributions of maternal and fetal DNA in maternal plasma publication-title: Clin Chem doi: 10.1373/clinchem.2003.024893 – volume: 112 start-page: E1317 year: 2015 ident: 2022060622181420700_bib13 article-title: Lengthening and shortening of plasma DNA in hepatocellular carcinoma patients publication-title: Proc Natl Acad Sci U S A doi: 10.1073/pnas.1500076112 – volume: 11 start-page: R106 year: 2010 ident: 2022060622181420700_bib17 article-title: Differential expression analysis for sequence count data publication-title: Genome Biol doi: 10.1186/gb-2010-11-10-r106 – volume: 106 start-page: 202 year: 2020 ident: 2022060622181420700_bib25 article-title: The biology of cell-free DNA fragmentation and the roles of DNASE1, DNASE1L3, and DFFB publication-title: Am J Hum Genet doi: 10.1016/j.ajhg.2020.01.008 – volume: 27 start-page: 1231 year: 2017 ident: 2022060622181420700_bib18 article-title: 5-Hydroxymethylcytosine signatures in cell-free DNA provide information about tumor types and stages publication-title: Cell Res doi: 10.1038/cr.2017.106 – volume: 351 start-page: 1329 year: 1998 ident: 2022060622181420700_bib8 article-title: Presence of donor-specific DNA in plasma of kidney and liver-transplant recipients publication-title: Lancet doi: 10.1016/S0140-6736(05)79055-3 – volume: 112 start-page: E5503 year: 2015 ident: 2022060622181420700_bib12 article-title: Plasma DNA tissue mapping by genome-wide methylation sequencing for noninvasive prenatal, cancer, and transplantation assessments publication-title: Proc Natl Acad Sci U S A doi: 10.1073/pnas.1508736112 – volume: 63 start-page: 606 year: 2017 ident: 2022060622181420700_bib24 article-title: Gestational age assessment by methylation and size profiling of maternal plasma DNA: a feasibility study publication-title: Clin Chem doi: 10.1373/clinchem.2016.265702 – volume: 64 start-page: 1239 year: 2018 ident: 2022060622181420700_bib22 article-title: Liver- and colon-specific DNA methylation markers in plasma for investigation of colorectal cancers with or without liver metastases publication-title: Clin Chem doi: 10.1373/clinchem.2018.290304 |
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Snippet | Plasma DNA fragmentomics is an emerging area of research covering plasma DNA sizes, end points, and nucleosome footprints. In the present study, we found a... |
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Title | Plasma DNA End-Motif Profiling as a Fragmentomic Marker in Cancer, Pregnancy, and Transplantation |
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