Establishment of a New Scirrhous Gastric Cancer Cell Line with FGFR2 Overexpression, OCUM-14.


Journal

Annals of surgical oncology
ISSN: 1534-4681
Titre abrégé: Ann Surg Oncol
Pays: United States
ID NLM: 9420840

Informations de publication

Date de publication:
Apr 2019
Historique:
received: 27 08 2018
pubmed: 18 1 2019
medline: 10 7 2019
entrez: 18 1 2019
Statut: ppublish

Résumé

The prognosis of scirrhous gastric carcinoma (SGC), which is characterized by rapid infiltration and proliferation of cancer cells accompanied by extensive stromal fibrosis, is extremely poor. In this study, we report the establishment of a unique SGC cell line from a gastric cancer patient in whom an autopsy was performed. A new SGC cell line, OCUM-14, was established from malignant ascites of a male patient with SGC. A postmortem autopsy was performed on the patient. Characterization of OCUM-14 cells was analyzed by microscopic examination, reverse transcription polymerase chain reaction, fluorescence in situ hybridization analysis, immunohistochemical examination, CCK-8 assay, and in vivo assay. OCUM-14 cells grew singly or in clusters, and were floating and round-shaped. Most OCUM-14 cells had many microvilli on their surfaces. The doubling time was 43.1 h, and the subcutaneous inoculation of 1.0 × 10 A new gastric cancer cell line, OCUM-14, was established from SGC and showed FGFR2 overexpression. OCUM-14 might be useful for elucidating the characteristic mechanisms of SGC and clarifying the effect of FGFR2 inhibitors on SGC.

Sections du résumé

BACKGROUND BACKGROUND
The prognosis of scirrhous gastric carcinoma (SGC), which is characterized by rapid infiltration and proliferation of cancer cells accompanied by extensive stromal fibrosis, is extremely poor. In this study, we report the establishment of a unique SGC cell line from a gastric cancer patient in whom an autopsy was performed.
METHODS METHODS
A new SGC cell line, OCUM-14, was established from malignant ascites of a male patient with SGC. A postmortem autopsy was performed on the patient. Characterization of OCUM-14 cells was analyzed by microscopic examination, reverse transcription polymerase chain reaction, fluorescence in situ hybridization analysis, immunohistochemical examination, CCK-8 assay, and in vivo assay.
RESULTS RESULTS
OCUM-14 cells grew singly or in clusters, and were floating and round-shaped. Most OCUM-14 cells had many microvilli on their surfaces. The doubling time was 43.1 h, and the subcutaneous inoculation of 1.0 × 10
CONCLUSION CONCLUSIONS
A new gastric cancer cell line, OCUM-14, was established from SGC and showed FGFR2 overexpression. OCUM-14 might be useful for elucidating the characteristic mechanisms of SGC and clarifying the effect of FGFR2 inhibitors on SGC.

Identifiants

pubmed: 30652228
doi: 10.1245/s10434-018-07145-2
pii: 10.1245/s10434-018-07145-2
doi:

Substances chimiques

Antineoplastic Agents 0
FGFR2 protein, human EC 2.7.10.1
Receptor, Fibroblast Growth Factor, Type 2 EC 2.7.10.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1093-1102

Subventions

Organisme : Japan Society for the Promotion of Science
ID : JP18H02883
Organisme : Japan Society for the Promotion of Science
ID : JP23390329

Auteurs

Tomohisa Okuno (T)

Department of Surgical Oncology, Osaka City University Graduate School of Medicine, Osaka City, Osaka, Japan.
Molecular Oncology and Therapeutics, Osaka City University Graduate School of Medicine, Osaka City, Japan.
Cancer Center for Translational Research, Osaka City University Graduate School of Medicine, Osaka City, Japan.

Masakazu Yashiro (M)

Department of Surgical Oncology, Osaka City University Graduate School of Medicine, Osaka City, Osaka, Japan. m9312510@med.osaka-cu.ac.jp.
Molecular Oncology and Therapeutics, Osaka City University Graduate School of Medicine, Osaka City, Japan. m9312510@med.osaka-cu.ac.jp.
Cancer Center for Translational Research, Osaka City University Graduate School of Medicine, Osaka City, Japan. m9312510@med.osaka-cu.ac.jp.

Go Masuda (G)

Department of Surgical Oncology, Osaka City University Graduate School of Medicine, Osaka City, Osaka, Japan.

Shingo Togano (S)

Department of Surgical Oncology, Osaka City University Graduate School of Medicine, Osaka City, Osaka, Japan.
Molecular Oncology and Therapeutics, Osaka City University Graduate School of Medicine, Osaka City, Japan.
Cancer Center for Translational Research, Osaka City University Graduate School of Medicine, Osaka City, Japan.

Kenji Kuroda (K)

Department of Surgical Oncology, Osaka City University Graduate School of Medicine, Osaka City, Osaka, Japan.
Molecular Oncology and Therapeutics, Osaka City University Graduate School of Medicine, Osaka City, Japan.
Cancer Center for Translational Research, Osaka City University Graduate School of Medicine, Osaka City, Japan.

Yuichiro Miki (Y)

Department of Surgical Oncology, Osaka City University Graduate School of Medicine, Osaka City, Osaka, Japan.
Molecular Oncology and Therapeutics, Osaka City University Graduate School of Medicine, Osaka City, Japan.
Cancer Center for Translational Research, Osaka City University Graduate School of Medicine, Osaka City, Japan.

Kosei Hirakawa (K)

Department of Surgical Oncology, Osaka City University Graduate School of Medicine, Osaka City, Osaka, Japan.

Masahiko Ohsawa (M)

Department of Diagnostic Pathology, Osaka City University Graduate School of Medicine, Osaka City, Japan.

Hideki Wanibuchi (H)

Molecular Pathology, Osaka City University Graduate School of Medicine, Osaka City, Japan.

Masaichi Ohira (M)

Department of Surgical Oncology, Osaka City University Graduate School of Medicine, Osaka City, Osaka, Japan.

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Classifications MeSH