Evidence map›Paper›PMID 42658353›Full record

ArticleHuman cell2026

Establishment of a patient-derived malignant peripheral nerve sheath tumor organoid model reveals SHH pathway activation and therapeutic vulnerability.

Haruki Matsuoka, Keiichi Yoshida, Yukiko Matsuoka, Satoru Sasagawa, Noriko Nagamine, Yoji Kukita, Hideaki Sabe, Yusuke Yoshimura, Haruna Takami, Rie Suzuki and 10 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

20 authors.

Haruki MatsuokaDepartment of Musculoskeletal Oncology Service, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-Ku, Osaka, 541-8567, Japan.
Keiichi YoshidaNext-Generation Precision Medicine Research Center, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-Ku, Osaka, 541-8567, Japan.
Yukiko MatsuokaNext-Generation Precision Medicine Research Center, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-Ku, Osaka, 541-8567, Japan.
Satoru SasagawaMolecular Biology Laboratory, Research Institute, Nozaki Tokushukai Hospital, Tanigawa 2-10-50, Daito, Osaka, 574-0074, Japan.
Noriko NagamineDepartment of Musculoskeletal Oncology Service, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-Ku, Osaka, 541-8567, Japan.
Yoji KukitaLaboratory of Genomic Pathology, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-Ku, Osaka, 541-8567, Japan.
Hideaki SabeDepartment of Musculoskeletal Oncology Service, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-Ku, Osaka, 541-8567, Japan.
Yusuke YoshimuraDepartment of Musculoskeletal Oncology Service, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-Ku, Osaka, 541-8567, Japan.
Haruna TakamiDepartment of Orthopaedic Surgery, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Rie SuzukiDepartment of Musculoskeletal Oncology Service, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-Ku, Osaka, 541-8567, Japan.
Hironari TamiyaDepartment of Musculoskeletal Oncology Service, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-Ku, Osaka, 541-8567, Japan.
Shigeki KakunagaDepartment of Musculoskeletal Oncology Service, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-Ku, Osaka, 541-8567, Japan.
Toshinari YagiDepartment of Musculoskeletal Oncology Service, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-Ku, Osaka, 541-8567, Japan.
Takafumi YokotaDepartment of Hematology, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-Ku, Osaka, 541-8567, Japan.
Sho NakaiDepartment of Orthopaedic Surgery, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Yoshinori ImuraDepartment of Orthopaedic Surgery, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Seiji OkadaDepartment of Orthopaedic Surgery, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Ken-Ichi YoshidaDepartment of Diagnostic Pathology and Cytology, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-Ku, Osaka, 541-8567, Japan.
Satoshi TakenakaDepartment of Musculoskeletal Oncology Service, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-Ku, Osaka, 541-8567, Japan.
Toru WakamatsuDepartment of Musculoskeletal Oncology Service, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-Ku, Osaka, 541-8567, Japan. evolutionhhh49@yahoo.co.jp.ORCID http://orcid.org/0000-0002-3073-0595

Funding

Japan Society for the Promotion of Science 23K06758Japan Society for the Promotion of Science JP23K08600
6 · The paper itself

Abstract

Malignant peripheral nerve sheath tumor (MPNST) is a rare and aggressive soft tissue sarcoma of presumed peripheral nerve sheath origin, for which effective systemic therapies remain limited. The biological mechanisms underlying its progression and therapeutic vulnerabilities are not fully understood, partly due to the lack of reliable patient-derived models. In this study, we attempted to establish organoid cultures from two clinically and pathologically unusual cases of MPNST using a modified air-liquid interface method. A stable organoid line was successfully generated from one case, and a corresponding organoid-derived xenograft (ODX) model was established. Both the organoid and ODX retained the histological, immunophenotypic, and genomic features of the original tumor. Comparative molecular analyses revealed shared copy number alterations involving NF1 and SUZ12 in both cases, suggesting underlying biological similarity. In the organoid-forming case, whole-exome and transcriptomic analyses identified a loss-of-function alteration in PTCH1 and activation of the Sonic Hedgehog (SHH) signaling pathway. Consistent with these findings, treatment with the Smoothened inhibitor vismodegib significantly suppressed organoid growth and downregulated SHH-related gene expression. These results indicate that SHH pathway activation may represent a therapeutically actionable vulnerability in a subset of MPNST. Our study establishes a patient-derived organoid model of MPNST and highlights its utility as a preclinical platform for investigating tumor biology and evaluating targeted therapies in this rare malignancy.

Indexed as

Hedgehog ProteinsNerve Sheath NeoplasmsOrganoidsSignal TransductionAnilidesAnimalsFemaleGene ExpressionHumansPatched-1 ReceptorPyridinesAnilidesHedgehog ProteinsHhAntag691Patched-1 ReceptorPTCH1 protein, humanPyridinesSHH protein, humanMalignant peripheral nerve sheath tumor (MPNST)OrganoidPTCH1Sonic Hedgehog signalingVismodegib

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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.