Evidence map›Paper›PMID 42049877›Full record

ArticleScientific reports2026

In vivo dynamics of G-quadruplex DNA structures during liver regeneration in mice.

Takumi Ishizuka, Kham Mo Aung, Baljinnyam Lkham-Erdene, Koichi Yano, Toshiki Kubota, Fidya, Shinichiro Shirouzu, Makoto Ikenoue, Kengo Kai, Phyu Synn Oo and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Takumi Ishizuka *Department of Anatomy, Histochemistry and Cell Biology, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan. tishizuka@med.miyazaki-u.ac.jp.
Kham Mo Aung *Department of Anatomy, Histochemistry and Cell Biology, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan.
Baljinnyam Lkham-ErdeneDepartment of Anatomy, Histochemistry and Cell Biology, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan.
Koichi YanoDepartment of Anatomy, Histochemistry and Cell Biology, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan.
Toshiki KubotaDepartment of Anatomy, Histochemistry and Cell Biology, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan.
FidyaDepartment of Anatomy, Histochemistry and Cell Biology, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan.
Shinichiro ShirouzuDepartment of Anatomy, Histochemistry and Cell Biology, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan.
Makoto IkenoueDepartment of Anatomy, Histochemistry and Cell Biology, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan.
Kengo KaiDepartment of Anatomy, Histochemistry and Cell Biology, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan.
Phyu Synn OoDepartment of Anatomy, Histochemistry and Cell Biology, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan.
Narantsog ChoijookhuuDepartment of Anatomy, Histochemistry and Cell Biology, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan.
Yoshitaka HishikawaDepartment of Anatomy, Histochemistry and Cell Biology, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan. yhishi@med.miyazaki-u.ac.jp.

Funding

Japan Society for the Promotion of Science 24K08641Japan Society for the Promotion of Science 25K10146
6 · The paper itself

Abstract

Guanine-rich DNA sequences can form four-stranded structures known as G-quadruplexes (G4s), which play important roles in cellular processes. However, direct observation of G4 dynamics in tissues remains challenging. Here, we report the in vivo dynamics of G4s during mouse liver regeneration after partial hepatectomy (PHx) using a G4-specific antibody. G4-positive hepatocytes gradually increased after PHx, peaking at 36 h, and then decreased, with signals predominantly in nuclei of cells in the peripheral region between the periportal and midzonal regions. Notably, double immunofluorescence analysis of cell cycle markers revealed that G4-positive cells colocalize with EdU- and Cyclin A2-positive cells, suggesting that G4 structures are formed during the S to G2 phases of the cell cycle. In mice deficient in high-mobility group box 2 (HMGB2), a candidate G4-interacting protein, G4-positive cells were significantly reduced compared with wild-type controls, although the temporal peak was preserved. Spatial distribution of G4-positive hepatocytes was also altered in Hmgb2

Indexed as

DNAG-QuadruplexesLiver RegenerationAnimalsCell CycleHepatectomyHepatocytesHMGB2 ProteinLiverMaleMiceMice, KnockoutDNAHMGB2 ProteinG-quadruplexHMGB2Liver regenerationPartial hepatectomy

Identifiers

PMID42049877
PMCPMC13316107

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.