A quantification method of somatic mutations in normal tissues and their accumulation in pediatric patients with chemotherapy.


Journal

Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876

Informations de publication

Date de publication:
02 08 2022
Historique:
entrez: 27 7 2022
pubmed: 28 7 2022
medline: 30 7 2022
Statut: ppublish

Résumé

Somatic mutations are accumulated in normal human tissues with aging and exposure to carcinogens. If we can accurately count any passenger mutations in any single DNA molecule, since their quantity is much larger than driver mutations, we can sensitively detect mutation accumulation in polyclonal normal tissues. Duplex sequencing, which tags both DNA strands in one DNA molecule, enables accurate count of such mutations, but requires a very large number of sequencing reads for each single sample of human-genome size. Here, we reduced the genome size to 1/90 using the

Identifiants

pubmed: 35895679
doi: 10.1073/pnas.2123241119
pmc: PMC9351471
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2123241119

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Auteurs

Sho Ueda (S)

Division of Epigenomics, National Cancer Center Research Institute, Tokyo, Japan, 104-0045.
Department of Pathology, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan, 305-8576.
Department of Thoracic Surgery, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan, 305-8576.

Satoshi Yamashita (S)

Division of Epigenomics, National Cancer Center Research Institute, Tokyo, Japan, 104-0045.

Miho Nakajima (M)

Department of Pediatric Oncology, National Cancer Center Hospital, Tokyo, Japan, 104-0045.

Tadashi Kumamoto (T)

Department of Pediatric Oncology, National Cancer Center Hospital, Tokyo, Japan, 104-0045.

Chitose Ogawa (C)

Department of Pediatric Oncology, National Cancer Center Hospital, Tokyo, Japan, 104-0045.

Yu-Yu Liu (YY)

Division of Epigenomics, National Cancer Center Research Institute, Tokyo, Japan, 104-0045.

Harumi Yamada (H)

Division of Epigenomics, National Cancer Center Research Institute, Tokyo, Japan, 104-0045.

Emi Kubo (E)

Division of Epigenomics, National Cancer Center Research Institute, Tokyo, Japan, 104-0045.

Naoko Hattori (N)

Division of Epigenomics, National Cancer Center Research Institute, Tokyo, Japan, 104-0045.

Hideyuki Takeshima (H)

Division of Epigenomics, National Cancer Center Research Institute, Tokyo, Japan, 104-0045.

Mika Wakabayashi (M)

Division of Epigenomics, National Cancer Center Research Institute, Tokyo, Japan, 104-0045.

Naoko Iida (N)

Division of Genome Analysis Platform Development, National Cancer Center Research Institute, Tokyo, Japan, 104-0045.

Yuichi Shiraishi (Y)

Division of Genome Analysis Platform Development, National Cancer Center Research Institute, Tokyo, Japan, 104-0045.

Masayuki Noguchi (M)

Department of Pathology, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan, 305-8576.

Yukio Sato (Y)

Department of Thoracic Surgery, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan, 305-8576.

Toshikazu Ushijima (T)

Division of Epigenomics, National Cancer Center Research Institute, Tokyo, Japan, 104-0045.

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Classifications MeSH