Evidence map›Paper›PMID 42166078›Full record

ArticleBrain tumor pathology2026

Dual TERT promoter mutations in glioblastoma, IDH-wildtype: a case report with preclinical investigations.

Yohei Miyake, Kensuke Tateishi, Hinako Okagawa, Akihide Koyama, Emi Hirata, Kanoko Sasaoka, Shuna Saito, Shuto Fushimi, Manabu Natsumeda, Erika Muraoka and 3 more

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

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Yohei MiyakeDepartment of Neurosurgery, Graduate School of Medicine, Yokohama City University, 3-9 Fukuura, Kanazawa, Yokohama, 2360004, Japan.
Kensuke TateishiDepartment of Neurosurgery, Graduate School of Medicine, Yokohama City University, 3-9 Fukuura, Kanazawa, Yokohama, 2360004, Japan. ktate12@yokohama-cu.ac.jp.ORCID http://orcid.org/0000-0001-6895-9013
Hinako OkagawaLaboratory of Biopharmaceutical and Regenerative Science, Graduate School of Medical Science, Yokohama City University, Yokohama, Japan.
Akihide KoyamaDepartment of Legal Medicine, Graduate School of Medical and Dental Science, Niigata University, Niigata, Japan.
Emi HirataDepartment of Neurosurgery, Graduate School of Medicine, Yokohama City University, 3-9 Fukuura, Kanazawa, Yokohama, 2360004, Japan.
Kanoko SasaokaDepartment of Neurosurgery, Graduate School of Medicine, Yokohama City University, 3-9 Fukuura, Kanazawa, Yokohama, 2360004, Japan.
Shuna SaitoLaboratory of Biopharmaceutical and Regenerative Science, Graduate School of Medical Science, Yokohama City University, Yokohama, Japan.
Shuto FushimiDepartment of Neurosurgery, Graduate School of Medicine, Yokohama City University, 3-9 Fukuura, Kanazawa, Yokohama, 2360004, Japan.
Manabu NatsumedaDepartment of Neurosurgery, Brain Research Institute, Niigata University, Niigata, Japan.
Erika MuraokaDepartment of Diagnostic Pathology, Yokohama City University Hospital, Yokohama, Japan.
Shoji YamanakaDepartment of Diagnostic Pathology, Yokohama City University Hospital, Yokohama, Japan.
Satoshi FujiiDepartment of Diagnostic Pathology, Yokohama City University Hospital, Yokohama, Japan.
Tetsuya YamamotoDepartment of Neurosurgery, Graduate School of Medicine, Yokohama City University, 3-9 Fukuura, Kanazawa, Yokohama, 2360004, Japan.

Funding

Japan Society for the Promotion of Science 22K09210
6 · The paper itself

Abstract

Telomerase reverse transcriptase promoter (TERTp) mutations c.-124C > T (C228T) and c.-146C > T (C250T) are the most frequent single-nucleotide variants promoting telomerase activation in glioblastoma. Here, we describe a rare case of glioblastoma IDH-wildtype with dual TERTp mutations. Genomic analyses of multiregional tumor samples revealed co-occurring TERT C228T and C250T mutations across tumor regions, with variable copy number alterations of EGFR and CDKN2A. Notably, only the TERTp C228T mutation was retained in the corresponding patient-derived xenograft, accompanied by more extensive copy number alterations, implying a selective growth advantage for the TERT C228T-harboring subclone during tumor propagation in this case. These findings suggest that dual TERTp mutations may arise through subclonal evolutionary processes in glioblastoma and highlight telomere maintenance as a dynamic, heterogeneous process rather than invariably representing a fixed early oncogenic event.

Indexed as

Dual TERT promoter mutationsPatient-derived xenograft modelSubclone

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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.