Establishment and Characterization of a Novel Primitive Yolk Sac Tumour Cell Line, TC587.


Journal

Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988

Informations de publication

Date de publication:
Feb 2020
Historique:
received: 13 12 2019
revised: 22 12 2019
accepted: 23 12 2019
entrez: 5 2 2020
pubmed: 6 2 2020
medline: 20 3 2020
Statut: ppublish

Résumé

Yolk sac tumour (YST) is a rare malignant ovarian germ cell tumour that often occurs in young women or adolescents and exhibits an unfavourable outcome. To evaluate the biological behavior of carcinomas in vitro, permanent tumour cell lines are required. However, previously, only a few human YST cell lines have been established. Therefore, we aimed to establish a novel YST cell line. We established a novel YST cell line, TC587, from an adolescent patient with ovarian YST. The cell line expressed AFP and SALL4, the characteristics of YST. In addition, we evaluated somatic mutations using next-generation sequencing and revealed some pathogenic variants, including mutations in the NRAS, KIT, KMT2C, RSF1, and TP53 genes. The newly established TC587 cell line may represent an effective tool for developing treatments and conducting molecular analyses for YST.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
Yolk sac tumour (YST) is a rare malignant ovarian germ cell tumour that often occurs in young women or adolescents and exhibits an unfavourable outcome. To evaluate the biological behavior of carcinomas in vitro, permanent tumour cell lines are required. However, previously, only a few human YST cell lines have been established. Therefore, we aimed to establish a novel YST cell line.
MATERIALS AND METHODS METHODS
We established a novel YST cell line, TC587, from an adolescent patient with ovarian YST.
RESULTS RESULTS
The cell line expressed AFP and SALL4, the characteristics of YST. In addition, we evaluated somatic mutations using next-generation sequencing and revealed some pathogenic variants, including mutations in the NRAS, KIT, KMT2C, RSF1, and TP53 genes.
CONCLUSION CONCLUSIONS
The newly established TC587 cell line may represent an effective tool for developing treatments and conducting molecular analyses for YST.

Identifiants

pubmed: 32014918
pii: 40/2/759
doi: 10.21873/anticanres.14007
doi:

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

759-766

Informations de copyright

Copyright© 2020, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Takeshi Iwasaki (T)

Department of Anatomic Pathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Department of Diagnostic Pathology, Japan Community Healthcare Organization, Kyushu Hospital, Fukuoka, Japan.

Kenichi Kohashi (K)

Department of Anatomic Pathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

Masasuke Ohno (M)

Department of Neurosurgery, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.

Tomoaki Taguchi (T)

Department of Pediatric Surgery, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

Yoshinao Oda (Y)

Department of Anatomic Pathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan oda@surgpath.med.kyushu-u.ac.jp.

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