Associations of selenoprotein expression and gene methylation with the outcome of clear cell renal carcinoma

Selenoproteins are a ubiquitous class of proteins defined by having a selenocysteine amino acid residue. While many of the selenoproteins have been well characterized with important roles in oxidation-reduction reactions and hormone synthesis among others, there exist some whose biological roles are not as well understood as denoted by the “SELENO” root. In this study, we explored associations between the reported RNA levels of “SELENO” proteins and clear cell renal cell carcinoma (ccRCC), the most common subtype of renal carcinoma in the US. Utilizing The Cancer Genome Atlas (TCGA) alongside other in silico tools, we discovered higher mRNA expression of Selenoprotein I, T, and P was associated with better overall survival outcomes and differential expression of other selenoproteins based on tumor stage. Additionally, we uncovered relative hypomethylation among selenoproteins in primary ccRCC tumor samples compared to normal tissue. Network and enrichment analysis showed numerous genes through which selenoproteins may modulate cancer progression and outcomes such as DERL1, PNPLA2/3, MIEN1, and FOXO1 which have been well-described in other cancers. In light of our findings highlighting an association of selenoprotein methylation and expression patterns with ccRCC outcome, further wet lab research is warranted. [Display omitted] •Certain uncharacterized selenoproteins were linked to survival outcomes and tumor staging in clear cell renal carcinoma cases.•There was relative selenoproteins hypermethylation in primary tumor versus normal samples.•Both the endoplastic reticulum associated degradation (ERAD) pathway as well as those involving fatty acid metabolism were linked to these uncharacterized selenoproteins and may modulate their effect on cancer progression.