Papillary renal cell carcinoma (PRCC) accounts for about 10 percent of all renal cell
carcinomas, and the prognosis is poor for people with advanced disease. Interleukin-20
receptor subunit beta (IL20RB) is a single-pass type I membrane protein of the type II
cytokine receptor family and is related to the pathogenesis of chronic inflammation and
autoimmune diseases, including psoriasis, glaucoma, vitiligo, rheumatoid arthritis, and
inflammatory bowel disease. However, little has been reported on IL20RB with respect to
cancer, especially in PRCC. Thus, we performed this study to explore its biological
characteristics in PRCC. Data from the TCGA database were used to analyze the expression
and prognosis of IL20RB. qRT-PCR was used to detect the expression of IL20RB in PRCC cells
in vitro. After knockdown of IL20RB with small interfering RNA (siRNA)
technology, the proliferation, migration, and invasion of Ketr-3 cells and the expression
of related proteins in the epithelial-mesenchymal transition (EMT) pathway were measured
with Cell Counting Kit-8 (CCK-8), transwell, and western blot assays. The findings
demonstrated that the expression of IL20RB was upregulated in both PRCC tissues and cells
and that the high expression of IL20RB led to low overall survival (OS). Furthermore,
after knockdown of IL20RB in vitro, the proliferation, migration, and
invasion of Ketr-3 cells were reduced, and the expression of related proteins in the EMT
pathway declined, suggesting that IL20RB plays a vital role in PRCC through the EMT
pathway. These results reveal the biological significance of IL20RB in PRCC and provide
new insight for future targeted drugs.