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Expression of Irisin/FNDC5 in Cancer Cells and Stromal Fibroblasts of Non-Small Cell Lung Cancer.

Authors :
Nowinska, Katarzyna
Jablonska, Karolina
Pawelczyk, Konrad
Piotrowska, Aleksandra
Partynska, Aleksandra
Gomulkiewicz, Agnieszka
Ciesielska, Urszula
Katnik, Ewa
Grzegrzolka, Jedrzej
Glatzel-Plucinska, Natalia
Ratajczak-Wielgomas, Katarzyna
Podhorska-Okolow, Marzenna
Dziegiel, Piotr
Source :
Cancers. Oct2019, Vol. 11 Issue 10, p1538. 1p.
Publication Year :
2019

Abstract

Background: Recent in vitro studies have indicated that irisin inhibits proliferation, migration and epithelial-mesenchymal transition. Irisin expression has not been studied in tumour tissues of non-small cell lung cancer (NSCLC) patients yet. The aim of the study was to determine the irisin expression in NSCLCs in comparison to the clinicopathological factors and expression of TTF-1, p63 and Ki-67. Material and methods: Tissue microarrays with 729 NSCLC and 140 non-malignant lung tissue (NMLT) were used to perform immunohistochemical reactions. Laser Capture Microdissection (LCM) was used to collect cancer and stromal cells from NSCLCs. FNDC5 expression was tested for LCM samples, 75 NSCLCs and 25 NMLTs with the RT-PCR technique. Western-blot, immunofluorescence reaction and RT-PCR assays were performed on lung cancer cell lines. Results: Irisin expression was observed in NSCLC cancer cells and stromal fibroblasts. In cancer cells, irisin expression was decreased in higher grades (G) of malignancy, tumour size (T) and according to lymph node metastasis. In stromal cells, irisin expression was increased in higher G and advanced T. A shorter overall survival was observed in patients with higher irisin expression in NSCLC stromal cells. Conclusions: Irisin expression in stromal fibroblasts may influence cancer cell proliferation and may be a prognostic factor for survival in NSCLC. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20726694
Volume :
11
Issue :
10
Database :
Academic Search Index
Journal :
Cancers
Publication Type :
Academic Journal
Accession number :
139256381
Full Text :
https://doi.org/10.3390/cancers11101538