Evidence map›Paper›PMID 39473365›Full record

ArticleMolecular oncology2025

Assembly of glioblastoma tumoroids and cerebral organoids: a 3D in vitro model for tumor cell invasion.

Jieun Kim, Rokhyun Kim, Wonseok Lee, Gyu Hyun Kim, Seeun Jeon, Yun Jin Lee, Jong Seok Lee, Kyung Hyun Kim, Jae-Kyung Won, Woochan Lee and 7 more

Abstract read
In one paragraph

Article in Molecular oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

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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

17 authors.

Jieun KimDepartment of Anatomy and Cell Biology, Seoul National University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-7429-3403
Rokhyun KimMedical Research Center, Genomic Medicine Institute, Seoul National University, Seoul, Korea.ORCID https://orcid.org/0009-0005-8573-6504
Wonseok LeeDepartment of Anatomy and Cell Biology, Seoul National University College of Medicine, Seoul, Korea.
Gyu Hyun KimLaboratory of Synaptic Circuit Plasticity, Neural Circuits Research Group, Korea Brain Research Institute, Daegu, Korea.
Seeun JeonDepartment of Anatomy and Cell Biology, Seoul National University College of Medicine, Seoul, Korea.
Yun Jin LeeDepartment of Anatomy and Cell Biology, Seoul National University College of Medicine, Seoul, Korea.
Jong Seok LeeDivision of Pediatric Neurosurgery, Seoul National University Children's Hospital, Seoul, Korea.
Kyung Hyun KimDepartment of Anatomy and Cell Biology, Seoul National University College of Medicine, Seoul, Korea.
Jae-Kyung WonDepartment of Pathology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
Woochan LeeMedical Research Center, Genomic Medicine Institute, Seoul National University, Seoul, Korea.
Kyunghyuk ParkMedical Research Center, Genomic Medicine Institute, Seoul National University, Seoul, Korea.
Hyun Je KimDepartment of Biomedical Sciences, Seoul National University College of Medicine, Seoul, Korea.
Sun-Wha ImDepartment of Biochemistry and Molecular Biology, Kangwon National University School of Medicine, Chuncheon, Korea.
Kea Joo LeeLaboratory of Synaptic Circuit Plasticity, Neural Circuits Research Group, Korea Brain Research Institute, Daegu, Korea.
Chul-Kee ParkDepartment of Neurosurgery, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-2350-9876
Jong-Il KimMedical Research Center, Genomic Medicine Institute, Seoul National University, Seoul, Korea.ORCID https://orcid.org/0000-0002-7240-3744
Ji Yeoun LeeDepartment of Anatomy and Cell Biology, Seoul National University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-0464-7605

Funding

KBRI Basic Research Programs, South Korea 24-BR-01-03Ministry of Education 2020R1A6A1A03047972Ministry of Science and ICT, South Korea 2021M3E5D9021884Ministry of Science and ICT, South Korea 2022R1A2C109210712
6 · The paper itself

Abstract

Glioblastoma (GBM) has a fatal prognosis because of its aggressive and invasive characteristics. Understanding the mechanism of invasion necessitates an elucidation of the relationship between tumor cells and the tumor microenvironment. However, there has been a scarcity of suitable models to investigate this. In this study, we established a glioblastoma-cerebral organoid assembloid (GCOA) model by co-culturing patient-derived GBM tumoroids and human cerebral organoids. Tumor cells from the tumoroids infiltrated the cerebral organoids, mimicking the invasive nature of the parental tumors. Using time-lapse imaging, various invasion patterns of cancer cells within cerebral organoids resembling a normal tissue milieu were monitored. Both single- and collective-cell invasion was captured in real-time. We also confirmed the formation of an intercellular tumor network and tumor-normal-cell interactions. Furthermore, the transcriptomic characterization of GCOAs revealed distinct features of invasive tumor cells. Overall, this study established the GCOA as a three-dimensional (3D) in vitro assembloid model to investigate invasion mechanisms and interactions between tumor cells and their microenvironment.

Indexed as

Brain NeoplasmsGlioblastomaModels, BiologicalOrganoidsCell Line, TumorCoculture TechniquesHumansNeoplasm InvasivenessTumor Microenvironmentassembloidglioblastomainvasionorganoidtumor microtube

Identifiers

PMID39473365
PMCPMC11887666

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Registered trials

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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.