Identification of ACSL4 as a biomarker and contributor of ferroptosis in clear cell renal cell carcinoma

Acyl-CoA synthetase long-chain family member 4 (ACSL4) has been linked to the ferroptosis process and is implicated in the pathogenesis of tumors. Nevertheless, neither the expression levels of ACSL4 nor its prognostic significance in clear cell renal cell carcinoma (ccRCC) is completely understood at this time.

ACSL4, which is a mediator and monitor of ferroptosis, was lowered in expression in ccRCC and acted as a valuable diagnostic and prognostic biological marker, thus representing a novel promising treatment target for ccRCC.

Predictions of the ACSL4 mRNA expression in ccRCC and its link to ccRCC prognosis were made based on data from the Oncomine and The Cancer Genome Atlas (TCGA) databases. Through the use of real-time polymerase chain reaction (PCR), we ascertained the levels of ACSL4 expression in human RCC samples. Analyses of the link between ACSL4 expression and the survival of ccRCC patients were undertaken using the Kaplan-Meier (KM) plotter database. To study the function that ACSL4 plays in ferroptosis in ccRCC cell lines, either upregulation or knockdown of its expression was performed.

We found that the ACSL4 expression level was considerably down-modulated in ccRCC samples (P<0.001), which was in line with the analytical results of the Oncomine and TCGA database. The subsequent immunohistochemistry findings revealed that ACSL4 levels in ccRCC samples were much lower or not undetectable in contrast with those in normal samples. The level of differential ACSL4 expression was strongly associated with factors such as disease stages, gender, tumor grade, nodal invasion, and ccRCC subtypes (all P<0.001). According to the results of the survival analysis, the overall survival was satisfactory among ccRCC patients who had overexpressed ACSL4 (P=0.014). In cancer cells, ferroptosis sensitization may be restored by overexpressing ACSL4 via the process of transfection; however, increasing ferroptosis resistance can be achieved by suppressing ACSL4 expression through the use of shRNA. Protein ubiquitination could have a function in influencing the way that ACSL4-induced ferroptosis works mechanically. Conclusions: ACSL4, which is a mediator and monitor of ferroptosis, was lowered in expression in ccRCC and acted as a valuable diagnostic and prognostic biological marker, thus representing a novel promising treatment target for ccRCC.