Evidence map›Paper›PMID 32348439›Full record

ArticleJournal of applied oral science : revista FOB2020

Ameloblastoma cell lines derived from different subtypes demonstrate distinct developmental patterns in a novel animal experimental model.

Takao Fuchigami, Hajime Suzuki, Takuya Yoshimura, Toshiro Kibe, Elissa Chairani, Tohru Kiyono, Michiko Kishida, Shosei Kishida, Norifumi Nakamura

Abstract read
In one paragraph

Article in Journal of applied oral science : revista FOB, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Molecular biological findings of ameloblastoma.The Japanese dental science review · 2021
    Review
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

9 authors.

Takao FuchigamiDepartment of Oral and Maxillofacial Surgery, School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.
Hajime SuzukiDepartment of Oral and Maxillofacial Surgery, School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.
Takuya YoshimuraDepartment of Oral and Maxillofacial Surgery, School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.
Toshiro KibeDepartment of Oral and Maxillofacial Surgery, School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.
Elissa ChairaniDepartment of Oral and Maxillofacial Surgery, School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.
Tohru KiyonoNational Cancer Center Research Institute, Tokyo, Japan.
Michiko KishidaDepartment of Biochemistry and Genetics, School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.
Shosei KishidaDepartment of Biochemistry and Genetics, School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.
Norifumi NakamuraDepartment of Oral and Maxillofacial Surgery, School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective Ameloblastoma is a representative odontogenic tumor comprising several characteristic invasive forms, and its pathophysiology has not been sufficiently elucidated. A stable animal experimental model using immortalized cell lines is crucial to explain the factors causing differences among the subtypes of ameloblastoma, but this model has not yet been disclosed. In this study, a novel animal experimental model has been established, using immortalized human ameloblastoma-derived cell lines. Methodology Ameloblastoma cells suspended in Matrigel were subcutaneously transplanted into the heads of immunodeficient mice. Two immortalized human ameloblastoma cell lines were used: AM-1 cells derived from the plexiform type and AM-3 cells derived from the follicular type. The tissues were evaluated histologically 30, 60, and 90 days after transplantation. Results Tumor masses formed in all transplanted mice. In addition, the tumors formed in each group transplanted with different ameloblastoma cells were histologically distinct: the tumors in the group transplanted with AM-1 cells were similar to the plexiform type, and those in the group transplanted with AM-3-cells were similar to the follicular type. Conclusions A novel, stable animal experimental model of ameloblastoma was established using two cell lines derived from different subtypes of the tumor. This model can help clarify its pathophysiology and hasten the development of new ameloblastoma treatment strategies.

Indexed as

Disease Models, AnimalAmeloblastomaAnimalsCell Line, TumorCells, CulturedCollagenDrug CombinationsFemaleGreen Fluorescent ProteinsImmunohistochemistryLamininMiceNeoplasms, ExperimentalProteoglycansReproducibility of ResultsTime FactorsCollagenDrug CombinationsGreen Fluorescent ProteinsLamininmatrigelProteoglycans

Identifiers

PMID32348439
PMCPMC7185982

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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.