Evidence map›Paper›PMID 39769375›Full record

ReviewInternational journal of molecular sciences2024

Tumorigenesis Caused by Aberrant Expression of GANP, a Central Component in the Mammalian TREX-2 Complex-Lessons from Transcription-Coupled DNA Damages.

Andri Rezano, Naomi Gondo, Yasuhiro Sakai, Yuko Nakamura, Suchada Phimsen, Tokio Tani, Akihiko Ito, Seiji Okada, Kazuhiko Kuwahara

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
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

9 authors.

Andri RezanoDepartment of Biomedical Sciences, Division of Cell Biology, Faculty of Medicine, Universitas Padjadjaran, Sumedang 45363, West Java, Indonesia.ORCID 0000-0003-2550-8794
Naomi GondoDepartment of Breast and Thyroid Surgical Oncology, Sagara Hospital, Kagoshima 892-0833, Kagoshima, Japan.
Yasuhiro SakaiDepartment of Tumor Pathology, Hamamatsu University School of Medicine, Hamamatsu 431-3192, Shizuoka, Japan.ORCID 0000-0001-7210-9249
Yuko NakamuraDepartment of Diagnostic Pathology, Kindai University Hospital, Osaka-sayama 589-8511, Osaka, Japan.
Suchada PhimsenDepartment of Biochemistry, Faculty of Medical Science, Naresuan University, Phitsanulok 65000, Thailand.ORCID 0000-0002-1949-427X
Tokio TaniInternational Research Center for Agricultural and Environmental Biology (IRCAEB), Kumamoto University, Kumamoto 860-8555, Kumamoto, Japan.
Akihiko ItoDepartment of Pathology, Kindai University Faculty of Medicine, Osaka-sayama 589-8511, Osaka, Japan.
Seiji OkadaDivision of Hematopoiesis, Joint Research Center for Retroviral Infection, Kumamoto University, Kumamoto 860-0811, Kumamoto, Japan.ORCID 0000-0003-3124-5206
Kazuhiko KuwaharaDepartment of Diagnostic Pathology and Genome Medical Center, Kindai University Hospital, Osaka-sayama 589-8511, Osaka, Japan.ORCID 0000-0002-7739-2183

Funding

The Japan Society for the Promotion of Science Grants-in-Aid for Scientific Research (C), grant number 23K06436
6 · The paper itself

Abstract

DNA is frequently damaged by genotoxic stresses such as ionizing radiation, reactive oxygen species, and nitrogen species. DNA damage is a key contributor to cancer initiation and progression, and thus the precise and timely repair of these harmful lesions is required. Recent studies revealed transcription as a source of genome instability, and transcription-coupled DNA damage has been a focus in cancer research. Impaired mRNA export is closely related to DNA damage through R-loop formation. The molecular machineries of transcription-coupled DNA damage have been extensively analyzed in

Indexed as

CarcinogenesisDNA DamageAcetyltransferasesAnimalsExodeoxyribonucleasesGene Expression Regulation, NeoplasticHumansIntracellular Signaling Peptides and ProteinsMiceNeoplasmsNuclear ProteinsPhosphoproteinsTranscription, GeneticAcetyltransferasesExodeoxyribonucleasesIntracellular Signaling Peptides and ProteinsMCM3AP protein, humanNuclear ProteinsPhosphoproteinsTREX2 protein, humancancerchemosensitivityGANPtranscription-coupled DNA damageTREX-2 complex

Identifiers

PMID39769375
PMCPMC11727803

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.