GNPNAT1 promotes the stemness of breast cancer and serves as a potential prognostic biomarker

Oncol Rep. 2023 Aug;50(2):157. doi: 10.3892/or.2023.8594. Epub 2023 Jun 30.

Abstract

Glucosamine‑phosphate N‑acetyltransferase 1 (GNPNAT1) is a member of the acetyltransferase superfamily, related to general control non‑depressible 5 (GCN5). It has been documented that GNPNAT1 expression is increased in lung cancer, whereas its involvement in breast cancer (BC) remains to be further investigated. The present study aimed to evaluate the expression levels of GNPNAT1 in BC and its effect on BC stem cells (BCSCs). The Cancer Genome Atlas (TCGA) database was used for the analysis of the expression of GNPNAT1 and its clinical significance. Cox regression and logistic regression analyses were used to evaluate prognosis‑related factors. The GNPNAT1‑binding protein network was constructed using the Search Tool for the Retrieval of Interacting Genes/Proteins (STRING) application. The biological signaling pathways implicated in GNPNAT1 were investigated through function enrichment analysis including Gene Ontology, Kyoto Encyclopedia of Genes and Genomes, and gene set enrichment analysis. The single‑sample GSEA method was used to investigate the connection between the level of immune infiltration and GNPNAT1 expression in BC. GNPNAT1 expression was upregulated in patients with BC and was significantly associated with a poor prognosis. GNPNAT1 and its co‑expressed genes were mostly enriched in nuclear transport, Golgi vesicle transport, ubiquitin‑like protein transferase activity and ribonucleoprotein complex binding, as determined using functional enrichment analysis. GNPNAT1 expression was positively associated with Th2 cells and T‑helper cells, and negatively associated with plasmacytoid dendritic cells, CD8+ T‑cells and cytotoxic cells. Additionally, the GNPNAT1 expression levels were considerably increased in BCSCs. GNPNAT1 knockdown markedly decreased the stemness ability of SKBR3 and Hs578T cells, including the production of CSC markers and mammosphere or clone formation, while GNPNAT1 overexpression increased the stemness level. Hence, the findings of the present study demonstrate that GNPNAT1 may be exploited as a novel prognostic biomarker and therapeutic target for BC.

Keywords: breast cancer; breast cancer stem cells; glucosamine‑phosphate N‑acetyltransferase 1; immune infiltration; prognosis.

MeSH terms

  • Acetyltransferases
  • Biomarkers
  • Breast Neoplasms* / genetics
  • CD8-Positive T-Lymphocytes
  • Female
  • Glucosamine 6-Phosphate N-Acetyltransferase
  • Humans
  • Prognosis

Substances

  • Acetyltransferases
  • Biomarkers
  • GNPNAT1 protein, human
  • Glucosamine 6-Phosphate N-Acetyltransferase

Grants and funding

The present study was supported by the National Natural Science Foundation of China (grant nos. 31501149, 31770815 and 31570764), the Wuhan Health and Family Planning Scientific Research Project (grant no. WX21Q49), the Hubei Natural Science Foundation (grant nos. 2017CFB537, 2019CFB398, 2019CFB368 and 2021CFB230), the Educational Commission of Hubei (grant no. B2020001), the Hubei Province Health and Family Planning Scientific Research Project (grant nos. WJ2021Q051, WJ2019M255 and ZY2021Q005), the Frontier Project of Applied Basic Research in Wuhan (grant no. 2020020601012250) and the Hunan Provincial Natural Science Foundation (grant no. 2023JJ50296) and ‘The 14th Five Year Plan’ Hubei Provincial advantaged characteristic disciplines (group) project of Wuhan University of Science and Technology (grant no. 2023C0303).