Evidence map›Paper›PMID 39625530›Full record

ArticleHuman cell2024

Establishment and characterization of the novel myxofibrosarcoma cell line, SMU-MFS.

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

Abstract read
PubMed Publisher
In one paragraph

Article in Human cell, 2024. 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
Kohichi TakadaDepartment of Medical Oncology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Yasutaka MurahashiDepartment of Orthopaedic Surgery, Sapporo Medical University School of Medicine, West 16, South 1, Chuo-ku, Sapporo, 060-8543, Japan.
Junya ShimizuDepartment 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.
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.
Akira TakasawaDepartments of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Kousuke IbaDepartment of Musculoskeletal Anti-Aging Medicine, Sapporo Medical University, Sapporo, Japan.
Atsushi TeramotoDepartment of Orthopaedic Surgery, Sapporo Medical University School of Medicine, West 16, South 1, Chuo-ku, Sapporo, 060-8543, Japan.
Makoto OsanaiDepartments of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.

Funding

JSPS KAKENHI 23K08657
6 · The paper itself

Abstract

Myxofibrosarcoma (MFS) is one of the most common soft-tissue sarcomas in elderly patients. Owing to the limited efficacy of chemotherapy and radiotherapy, complete resection is the only available curative treatment. Therefore, developing novel therapies for MFS is important to improve clinical outcomes. Herein, a novel MFS cell line, namely SMU-MFS, was established to better understand the biologic characteristics of MFS and develop new therapies. A tissue sample from the surgically resected tumor tissue of a 56-year-old patient with a tumor was subjected to primary culture. The cell line was established and authenticated by assessing the short tandem repeats of DNA microsatellites. The monolayer cultures of SMU-MFS cells exhibited constant growth, spheroid formation, and invasive capacity. Furthermore, the cells exhibited low chemosensitivity to doxorubicin, eribulin, and pazopanib, which are used to inhibit metastatic progression. In addition, of the four mice inoculated with SMU-MFS cells, tumors developed in two mice after 8 weeks. Altogether, the findings of this study suggest that the SMU-MFS cell line can be a useful tool for investigating MFS development and evaluating novel therapeutic agents.

Indexed as

FibrosarcomaPyrimidinesAnimalsAntineoplastic AgentsCell Line, TumorDoxorubicinFuransHumansIndazolesKetonesMaleMiceMiddle AgedPolyether PolyketidesSulfonamidesAntineoplastic AgentsDoxorubicineribulinFuransIndazolesKetonespazopanibPolyether PolyketidesPyrimidinesSulfonamidesCell lineChemotherapyLocal recurrenceMyxofibrosarcoma

Identifiers

What Socratic 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 Socratic graph.