DLAT is a promising prognostic marker and therapeutic target for hepatocellular carcinoma : a comprehensive study based on public databases

© 2023. Springer Nature Limited..

Cuproptosis is a new mechanism of cell death that differs from previously identified regulatory cell death mechanisms. Cuproptosis induction holds promise as a new tumour treatment. Therefore, we investigated the value of cuproptosis-related genes in the management of hepatocellular carcinoma (HCC). The cuproptosis-related gene Dihydrolipoamide S-Acetyltransferase (DLAT) were significantly upregulated in liver cancer tissues. High levels of DLAT were an independent prognostic factor for shorter overallsurvival (OS) time. DLAT and its related genes were mainly involved in cell metabolism, tumor progression and immune regulation. DLAT was significantly associated with the level of immune cell infiltration and immune checkpoints in HCC. HCC with high DLAT expression was predicted to be more sensitive to sorafenib treatment. The risk prognostic signature established based on DLAT and its related genes had a good prognostic value. The cuproptosis-related gene DLAT is a promising independent prognostic marker and therapeutic target in HCC. The new prognostic signature can effectively predict the prognosis of HCC patients.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:13

Enthalten in:

Scientific reports - 13(2023), 1 vom: 12. Okt., Seite 17295

Sprache:

Englisch

Beteiligte Personen:

Zhang, Peng [VerfasserIn]
Zhao, Jiang-Hua [VerfasserIn]
Yuan, Liu-Xia [VerfasserIn]
Ju, Lin-Ling [VerfasserIn]
Wang, Hui-Xuan [VerfasserIn]
Wang, Feng [VerfasserIn]
Chen, Lin [VerfasserIn]
Cai, Wei-Hua [VerfasserIn]

Links:

Volltext

Themen:

9ZOQ3TZI87
Dihydrolipoyllysine-Residue Acetyltransferase
EC 2.3.1.12
Journal Article
Research Support, Non-U.S. Gov't
Sorafenib

Anmerkungen:

Date Completed 17.11.2023

Date Revised 19.11.2023

published: Electronic

Citation Status MEDLINE

doi:

10.1038/s41598-023-43835-y

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM36321108X