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Perilipin 1 Expression Differentiates Liposarcoma from Other Types of Soft Tissue Sarcoma

Authors :
Lena Maria Pawella
Gunhild Mechtersheimer
Beate K. Straub
Wilfried Roth
Hagen Roland Witzel
Peter Schirmacher
Marcus Renner
E Eiteneuer
Merita Hashani
Source :
The American Journal of Pathology. 189:1547-1558
Publication Year :
2019
Publisher :
Elsevier BV, 2019.

Abstract

Lipid droplets, a morphologic feature of adipocytic tumors, are strongly regulated by associated proteins of the perilipin/PAT (perilipin, adipophilin, and tail-interacting protein of 47 kD) family. So far, the use of perilipins as markers for differential diagnosis of soft tissue tumors has only been studied in a few cases. The aim of this study was to investigate the expression of perilipins in 478 human soft tissue tumors and 60 respective normal tissues. Perilipin 1 was immunohistochemically positive in all studied cases of well-differentiated liposarcomas, >90% of myxoid round cell liposarcomas, and >70% of pleomorphic liposarcomas, whereas only the differentiated components of dedifferentiated liposarcomas were immunohistochemically positive for perilipin 1. All other types of soft tissue sarcomas were negative for perilipin 1. Perilipin 2 was more prominent in dedifferentiated and pleomorphic liposarcomas and nearly all other high-grade sarcomas. In well-differentiated liposarcomas, lipomas, or normal adipose tissue, perilipin 2 was virtually absent. In addition, long-term stimulation of adipogenesis in the liposarcoma cell line LiSa-2 restored perilipin 1 expression, as exhibited in the source tumor. Furthermore, knockdown of perilipin 2 or perilipin 3 in LiSa-2 cells influenced lipid droplet number and size as well as cell vitality. In summary, perilipin 1 is a promising marker for the differential diagnosis of liposarcomas from other soft tissue sarcomas, whereas perilipin 2 correlates negatively with tumor grade and may be therapeutically useful.

Details

ISSN :
00029440
Volume :
189
Database :
OpenAIRE
Journal :
The American Journal of Pathology
Accession number :
edsair.doi.dedup.....07622db8c4f15779a186d0ee5fd4adcb
Full Text :
https://doi.org/10.1016/j.ajpath.2019.04.017