Long non-coding RNA PICSAR decreases adhesion and promotes migration of squamous carcinoma cells by downregulating α2β1 and α5β1 integrin expression.
Minna PiipponenJyrki HeinoVeli-Matti KähäriLiisa NissinenPublished in: Biology open (2018)
Long non-coding RNAs (lncRNAs) regulate various cellular processes, and they have emerged as potential biomarkers and therapeutic targets in cancer. We have previously characterized the oncogenic role of lncRNA PICSAR (p38 inhibited cutaneous squamous cell carcinoma associated lincRNA) in cutaneous squamous cell carcinoma (cSCC), the most common metastatic skin cancer. In this study, we show that knockdown of PICSAR in cSCC cells upregulates expression of α2, α5 and β1 integrins, resulting in increased cell adhesion and decreased cell migration on collagen I and fibronectin. In contrast, overexpression of PICSAR in cSCC cells downregulates expression of α2, α5 and β1 integrins on cell surface, resulting in decreased cell adhesion on collagen I and fibronectin and increased cell migration. These results demonstrate a novel mechanism for regulation of the expression of collagen and fibronectin binding integrins by lncRNA PICSAR, leading to altered adhesion and migration of cSCC cells.This article has an associated First Person interview with the first author of the paper.
Keyphrases
- long non coding rna
- poor prognosis
- cell migration
- cell adhesion
- squamous cell carcinoma
- induced apoptosis
- cell cycle arrest
- binding protein
- magnetic resonance
- cell surface
- endoplasmic reticulum stress
- transcription factor
- small cell lung cancer
- signaling pathway
- oxidative stress
- radiation therapy
- staphylococcus aureus
- cell proliferation
- biofilm formation
- tissue engineering
- pi k akt