Evidence map›Paper›PMID 41801630›Full record

ArticleHuman cell2026

Establishment and characterization of NCC-GCTB16-C1: novel patient-derived cell line of giant cell tumor of bone.

Kenta Kono, Yomogi Shiota, Julia Osaki, Ting-Ting Shu, Satoshi Kamio, Shintaro Iwata, Shogo Nishino, Akihiko Yoshida, Sumio Ohtsuki, Seiji Ohtori and 2 more

Abstract read
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In one paragraph

Article in Human cell, 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.

Kenta KonoDivision of Rare Cancer Research, National Cancer Center Research Institute, 5-1-1 Tsukiji, , Chuo-Ku, Tokyo, 104-0045, Japan.
Yomogi ShiotaDivision of Rare Cancer Research, National Cancer Center Research Institute, 5-1-1 Tsukiji, , Chuo-Ku, Tokyo, 104-0045, Japan.
Julia OsakiDivision of Rare Cancer Research, National Cancer Center Research Institute, 5-1-1 Tsukiji, , Chuo-Ku, Tokyo, 104-0045, Japan.
Ting-Ting ShuDivision of Rare Cancer Research, National Cancer Center Research Institute, 5-1-1 Tsukiji, , Chuo-Ku, Tokyo, 104-0045, Japan.
Satoshi KamioDepartment of Musculoskeletal Oncology and Rehabilitation Medicine, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-Ku, Tokyo, 104-0045, Japan.
Shintaro IwataDepartment of Musculoskeletal Oncology and Rehabilitation Medicine, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-Ku, Tokyo, 104-0045, Japan.
Shogo NishinoDepartment of Diagnostic Pathology, National Cancer Center Hospital, 5-1-1 Tsukiji, , Chuo-Ku, Tokyo, 104-0045, Japan.
Akihiko YoshidaDepartment of Diagnostic Pathology, National Cancer Center Hospital, 5-1-1 Tsukiji, , Chuo-Ku, Tokyo, 104-0045, Japan.
Sumio OhtsukiDepartment of Pharmaceutical Microbiology, Faculty of Life Sciences, Kumamoto University, 5-1 Oe-Honmachi, Chuo-Ku, Kumamoto, 862-0973, Japan.
Seiji OhtoriDepartment of Orthopaedic Surgery, Graduate School of Medicine, Chiba University, 1- 8-1 Inohana, Chuo-Ku, Chiba-Shi, 260- 0856, Japan.
Akira KawaiDepartment of Musculoskeletal Oncology and Rehabilitation Medicine, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-Ku, Tokyo, 104-0045, Japan.
Tadashi KondoDivision of Rare Cancer Research, National Cancer Center Research Institute, 5- 1-1Tsukiji, Chuo-Ku, Tokyo, 104- 0045, Japan. takondo@ncc.go.jp.ORCID http://orcid.org/0000-0001-6405-7792

Funding

AMED 256f0137009j0001AMED JP24ama121018JSPS KAKENHI 24K02574JSPS KAKENHI 25K12471JSPS KAKENHI 25K18360
6 · The paper itself

Abstract

Giant cell tumor of bone (GCTB) is a locally aggressive osteolytic bone tumor characterized by recurrent mutation in the H3-3A gene. Although surgical resection remains the mainstay of treatment, a considerable proportion of patients experience local recurrence or pulmonary metastasis, and effective systemic therapy has not yet been established. Given the inherent clinicopathological heterogeneity of GCTB, we established a novel patient-derived cell line, NCC-GCTB16-C1, from the primary tumor of a patient with GCTB to expand the experimental resources available for translational research. The cells exhibited stable proliferation over a 3-month period, retained the characteristic H3-3A mutation, and formed spheroids with variable morphologies under three-dimensional conditions. They also demonstrated invasive and migratory behavior consistent with the biological properties of GCTB. Proteomic analysis revealed that NCC-GCTB16-C1 exhibited properties similar to those of the original tumor tissue. Thus, NCC-GCTB16-C1 provides an in vitro model that faithfully reflects the molecular and phenotypic features of GCTB, offering a valuable tool for mechanistic studies and preclinical drug evaluation.

Indexed as

Bone NeoplasmsGiant Cell Tumor of BoneCell Line, TumorCell MovementCell ProliferationHistonesHumansMutationNeoplasm InvasivenessProteomicsH3-3A protein, humanHistonesBone tumorGiant cell tumor of bonePatient-derived modelProteomic analysisSarcoma

Identifiers

What Socratic holds

Textmetadata
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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 Socratic graph.