# WTAP-Mediated Glutaminase Splicing Bias Suppresses Ferroptosis in Hepatocellular Carcinoma

## TL;DR

This study shows how a protein called WTAP helps cancer cells resist a type of cell death called ferroptosis by changing how a gene called GLS is processed, which could lead to new cancer treatments.

## Contribution

The study reveals a novel mechanism where WTAP-mediated splicing of GLS promotes ferroptosis resistance in hepatocellular carcinoma.

## Key findings

- AKT phosphorylates WTAP at S176, enhancing its interaction with methyltransferase-like protein 3.
- WTAP-mediated m6A modification of GLS pre-mRNA favors splicing toward glutaminase C (GAC), promoting tumor growth.
- Increased GAC expression and WTAP pS176 levels correlate with poor prognosis in hepatocellular carcinoma patients.

## Abstract

Background: Hepatocellular carcinoma (HCC), a highly aggressive malignancy with poor prognosis, is characterized by hyperactivation of the epidermal growth factor receptor (EGFR) signaling pathway. Glutaminase (GLS) is commonly overexpressed in numerous malignant tumors and acts as an oncogene to support cell growth and tumor progression, making it a target for cancer treatment. This study aimed to elucidate the underlying mechanisms of EGFR activation in driving glutaminolysis reprogramming and conferring ferroptosis resistance in HCC. Methods: Untargeted metabolomics, stable isotope-assisted metabolomic analysis, and RNA sequencing analysis were utilized to elucidate the mechanisms underlying glutaminolysis reprogramming upon EGFR activation. Immunoprecipitation, RNA pulldown, and dual-luciferase reporter assays were employed to examine the regulatory role of Wilms’ tumor 1-associated protein (WTAP) phosphorylation in GLS alternative splicing. Flow cytometry, cell viability assays, tumor-bearing mouse models, and HCC clinical specimens were used to validate the role of the AKT–WTAP–GLS axis in ferroptosis resistance and tumor progression. Results: Here, we demonstrated that AKT activated by EGFR signaling phosphorylated WTAP S176 and increased WTAP binding to methyltransferase-like protein 3. The enhanced interaction promoted the site-specific N6-methyladenosine (m6A) modification of GLS pre-mRNA, which in turn favored the alternative splicing of GLS toward glutaminase C (GAC) over kidney-type glutaminase. This switch led to increased glutamine utilization and glutathione/nicotinamide adenine dinucleotide phosphate (reduced form) biosynthesis, thereby alleviating ferroptosis and promoting tumor growth in mice. In addition, the levels of WTAP pS176 and GAC expression, which were mutually correlated, were positively associated with poor prognosis of patients with HCC. Conclusions: These findings uncover a critical mechanism by which tumor cells counteract ferroptosis by WTAP-mediated GLS alternative splicing under EGFR activation, highlighting the therapeutic potential of targeting the m6A-dependent GLS isoform switch in HCC and offering a rationale for the development of combination therapies.