# GOT2: New therapeutic target in pancreatic cancer

**Authors:** Jiarui Bu, Zeyu Miao, Qing Yang

PMC · DOI: 10.1016/j.gendis.2024.101370 · 2024-07-02

## TL;DR

This paper explores GOT2 as a potential new target for treating pancreatic cancer by examining its role in metabolism and immunity.

## Contribution

The paper highlights GOT2's potential as a novel therapeutic target in pancreatic cancer.

## Key findings

- GOT2 is part of the malate-aspartate shuttle system and affects cellular redox balance.
- GOT2 influences amino acid metabolism and may impact cancer progression.
- GOT2's metabolic and immune effects could lead to new treatment strategies.

## Abstract

In recent years, the incidence and mortality rates of pancreatic cancer have been steadily increasing, and conventional therapies have shown a high degree of tolerance. Therefore, the search for new therapeutic targets remains a key issue in current research. Mitochondrial glutamic-oxaloacetic transaminase 2 (GOT2) is an important component of the malate-aspartate shuttle system, which plays an important role in the maintenance of cellular redox balance and amino acid metabolism, and has the potential to become a promising target for anti-cancer therapy. In this paper, we will elaborate on the metabolic and immune effects of GOT2 in pancreatic cancer based on existing studies, with a view to opening up new avenues for the treatment of pancreatic cancer.

## Linked entities

- **Genes:** GOT2 (glutamic-oxaloacetic transaminase 2) [NCBI Gene 2806]
- **Diseases:** pancreatic cancer (MONDO:0005192)

## Full-text entities

- **Genes:** GOT2 (glutamic-oxaloacetic transaminase 2) [NCBI Gene 2806] {aka DEE82, KAT4, KATIV, KYAT4, mitAAT}
- **Diseases:** pancreatic cancer (MESH:D010190), cancer (MESH:D009369)

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12005923/full.md

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Source: https://tomesphere.com/paper/PMC12005923