Association of Irisin/FNDC5 with ERRα and PGC-1α Expression in NSCLC.
Katarzyna NowińskaKarolina JabłońskaUrszula CiesielskaAleksandra PiotrowskaKatarzyna Haczkiewicz-LeśniakKonrad PawełczykMarzenna Podhorska-OkołówPiotr DzięgielPublished in: International journal of molecular sciences (2022)
The rapid growth and division of cancer cells are associated with mitochondrial biogenesis or switching to glycolysis. ERRα, PGC-1α and irisin/FNDC5 are some of the proteins that can influence these processes. The aim of this study was to determine the correlation of these proteins in non-small cell lung cancer (NSCLC) and to investigate their association with clinicopathological parameters. Immunohistochemistry reactions were performed on tissue microarrays (860 NSCLC, 140 non-malignant lung tissue). The normal fibroblast cell line (IMR-90) and lung cancer cell lines (NCI-H1703 and NCI-H522) were used as co-cultures. The mRNA levels of FNDC5 and ESRRA (encoding ERRα) were assessed in IMR-90 cells after co-culture with lung cancer cells. We observed a decreased level of ERRα with an increase in tumor size (T), stages of the disease, and lymph node metastases (N). In the adenocarcinoma (AC) subtype, patients with a higher ERRα expression had significantly longer overall survival. A moderate positive correlation was observed between FNDC5 mRNA and ESRRA mRNA in NSCLCs. The expression of FNDC5 mRNA in IMR-90 cells increased after 24 h, and ESRRA gene expression increased after 48 h of co-culture. The ERRα receptor with PGC-1α participates in the control of FNDC5/irisin expression. Normal fibroblasts revealed an upregulation of the FNDC5 and ESRRA genes under the influence of lung cancer cells.
Keyphrases
- poor prognosis
- binding protein
- small cell lung cancer
- gene expression
- lymph node
- induced apoptosis
- skeletal muscle
- long non coding rna
- cell cycle arrest
- squamous cell carcinoma
- oxidative stress
- radiation therapy
- early stage
- signaling pathway
- cell death
- high intensity
- tyrosine kinase
- brain metastases
- genome wide identification
- extracellular matrix
- locally advanced
- rectal cancer