# Downregulation of ZFP36L1 contributes to methotrexate resistance in osteosarcoma through enhanced NHEJ DNA repair mechanisms

## TL;DR

This study shows that lower levels of ZFP36L1 help osteosarcoma cells resist methotrexate by boosting DNA repair, suggesting ZFP36L1 could be a target to improve treatment.

## Contribution

The novel finding is that ZFP36L1 downregulation enhances NHEJ DNA repair, contributing to methotrexate resistance in osteosarcoma.

## Key findings

- ZFP36L1 overexpression increases methotrexate sensitivity in osteosarcoma cells.
- ZFP36L1 interacts with DCLRE1C mRNA, leading to its degradation and reduced NHEJ DNA repair efficiency.
- Downregulation of ZFP36L1 is linked to methotrexate resistance in osteosarcoma.

## Abstract

Chemotherapy resistance poses a significant challenge in the treatment of osteosarcoma. While DNA damage repair mechanisms play a crucial role in this resistance, effective intervention strategies remain limited. This study elucidates an intrinsic DNA damage repair mechanism in osteosarcoma cells treated with methotrexate (MTX) that can be effectively disrupted through the overexpression of ZFP36L1. Our findings indicate that ZFP36L1 expression is downregulated in MTX-resistant osteosarcoma cells. By overexpressing ZFP36L1 in osteosarcoma cell lines, we observed an increase in sensitivity to MTX. Further investigation revealed that the overexpression of ZFP36L1 reduces the efficiency of the DNA damage repair process, particularly by inhibiting the DCLRE1C-mediated non-homologous end joining (NHEJ) pathway. Through analysis of the 3′ untranslated region (3′UTR) of DCLRE1C mRNA, we identified 8 potential AU-rich elements (AREs) that bind to ZFP36L1. We demonstrated that ZFP36L1 directly interacts with DCLRE1C mRNA, leading to its degradation. In summary, decreased ZFP36L1 expression serves as an inherent mechanism enabling osteosarcoma to develop resistance to MTX therapy. These results highlight ZFP36L1 as a promising therapeutic target for overcoming MTX chemoresistance in osteosarcoma.