Evidence map›Paper›PMID 40691346›Full record

ArticleHuman cell2025

SMU-pRMS: a novel cell line of pleomorphic rhabdomyosarcoma.

Naoya Nakahashi, Makoto Emori, Yasutaka Murahashi, Kazuyuki Murase, Junya Shimizu, Kenji Murata, Tomohide Tsukahara, Shintaro Sugita, Kousuke Iba, Kohichi Takada and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Human cell, 2025. 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.

Naoya NakahashiDepartment of Orthopaedic Surgery, Sapporo Medical University School of Medicine, West 16, South 1, Chuo- Ku, Sapporo, 060-8543, Japan.
Makoto EmoriDepartment of Orthopaedic Surgery, Sapporo Medical University School of Medicine, West 16, South 1, Chuo- Ku, Sapporo, 060-8543, Japan. emrmkt@yahoo.co.jp.ORCID http://orcid.org/0000-0003-2512-2795
Yasutaka MurahashiDepartment of Orthopaedic Surgery, Sapporo Medical University School of Medicine, West 16, South 1, Chuo- Ku, Sapporo, 060-8543, Japan.
Kazuyuki MuraseDepartment of Medical Oncology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Junya ShimizuDepartment of Orthopaedic Surgery, Sapporo Medical University School of Medicine, West 16, South 1, Chuo- Ku, Sapporo, 060-8543, Japan.
Kenji MurataDepartments of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Tomohide TsukaharaDepartments of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Shintaro SugitaDepartment of Surgical Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Kousuke IbaSapporo-Minami Orthopedic Hospital, 4-11 South 33 West 11, Minami-Ku, Sapporo, Japan.
Kohichi TakadaDepartment of Medical Oncology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Makoto OsanaiDepartments of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Atsushi TeramotoDepartment of Orthopaedic Surgery, Sapporo Medical University School of Medicine, West 16, South 1, Chuo- Ku, Sapporo, 060-8543, Japan.

Funding

KAKENHI 23K08657
6 · The paper itself

Abstract

Pleomorphic rhabdomyosarcoma (pRMS) is a rare and highly malignant mesenchymal tumor. Complete resection is the only curative treatment available, owing to the limited efficacy of chemotherapy and radiotherapy. Therefore, developing novel therapies for pRMS is important for improving clinical outcomes. Herein, a novel pRMS cell line, SMU-pRMS, was established for a detailed understanding of the biological characteristics of pRMS, thereby developing new therapies. A tissue sample from a surgically resected tumor of a 69-year-old patient was subjected to primary culture. The cell line was established and authenticated by evaluating the short tandem repeats of DNA microsatellites. Monolayer cultures of SMU-pRMS cells exhibited constant growth, spheroid formation, and invasiveness. These cells exhibited high chemosensitivity to eribulin. In addition, mice inoculated with SMU-pRMS cells developed tumors after 4 weeks. Therefore, the SMU-pRMS cell line is a useful tool for investigating pRMS development and evaluating novel therapeutic agents.

Indexed as

RhabdomyosarcomaAgedAnimalsCell Line, TumorFuransHumansKetonesMaleMiceMicrosatellite RepeatsNeoplasm InvasivenessPolyether PolyketidesSpheroids, CellularTumor Cells, CulturederibulinFuransKetonesPolyether PolyketidesCell lineDNA microsatelliteEribulinPleomorphic rhabdomyosarcomaTumor

Identifiers

What OpenQuestion holds

Textmetadata
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.