The differential expression of perilipin-2 in hepatoblastoma and its association with prognosis.


Journal

Histology and histopathology
ISSN: 1699-5848
Titre abrégé: Histol Histopathol
Pays: Spain
ID NLM: 8609357

Informations de publication

Date de publication:
Nov 2021
Historique:
pubmed: 4 9 2021
medline: 1 4 2022
entrez: 3 9 2021
Statut: ppublish

Résumé

Perilipin-2, a lipid droplet (LD) coating protein, has been found to be involved in cancer progression. However, its role in hepatoblastoma (HB) is undefined. We collected 87 HB samples and the corresponding clinical data. Immunohistochemistry (IHC) staining was performed to detect perilipin-2 and the association of the perilipin-2 expression with clinical characteristics and prognosis was analyzed. The expression of perilipin-2 was increased in fetal HB components in comparison to embryonal HB components. The predominant staining pattern was vesicular in fetal HB cells, while it was granular in embryonal HB cells. Furthermore, strong expression of perilipin-2 was associated with the histopathological type of fetal predominant HB. Although event-free survival (EFS) did not differ to a statistically significant extent between the strong and weak expression groups in a univariate survival analysis, a multivariate survival analysis revealed that EFS was significantly improved in the strong perilipin-2 expression group. In conclusion, perilipin-2 is differentially expressed in HB and the strong expression of perilipin-2 predicts a better prognosis.

Identifiants

pubmed: 34477212
pii: HH-18-371
doi: 10.14670/HH-18-371
doi:

Substances chimiques

Perilipin-2 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1169-1178

Subventions

Organisme : Ministry of Education, Culture, Sports, Science and Technology, Tokyo, Japan
ID : 19K16783
Organisme : Ministry of Education, Culture, Sports, Science and Technology, Tokyo, Japan
ID : 20K07454
Organisme : Promoted Research from Kanazawa Medical University
ID : S2018-6

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Auteurs

Sadafumi Azukisawa (S)

Department of Gastroenterological Endoscopy, Kanazawa Medical University Hospital, Ishikawa, Japan.

Jianbo Zheng (J)

Department of Pathology and Laboratory Medicine, Kanazawa Medical University, Ishikawa, Japan.
Department of Pediatrics, Wuhan Union Hospital, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Hubei, China. jianbo@kanazawa-med.ac.jp.

Xin Guo (X)

Department of Pathology and Laboratory Medicine, Kanazawa Medical University, Ishikawa, Japan.
Department of Pathology, Kanazawa Medical University Hospital, Ishikawa, Japan.

Hiroki Ura (H)

Center for Clinical Genomics, Kanazawa Medical University Hospital, Ishikawa, Japan.
Division of Genomic Medicine, Department of Advanced Medicine, Medical Research Institute, Kanazawa Medical University, Ishikawa, Japan.

Yo Niida (Y)

Center for Clinical Genomics, Kanazawa Medical University Hospital, Ishikawa, Japan.
Division of Genomic Medicine, Department of Advanced Medicine, Medical Research Institute, Kanazawa Medical University, Ishikawa, Japan.

Tohru Itoh (T)

Department of Gastroenterological Endoscopy, Kanazawa Medical University Hospital, Ishikawa, Japan.

Sohsuke Yamada (S)

Department of Pathology and Laboratory Medicine, Kanazawa Medical University, Ishikawa, Japan.
Department of Pathology, Kanazawa Medical University Hospital, Ishikawa, Japan.

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