As3MT is related to relative RNAs and base modifications of p53 in workers exposed to arsenic

Environ Sci Pollut Res Int. 2023 May;30(22):62094-62103. doi: 10.1007/s11356-023-26457-9. Epub 2023 Mar 20.

Abstract

As3MT is the key enzyme involved in the methylation metabolism of arsenic. It is associated with DNA methylation closely also. This study is to explore the relationships between As3MT and epigenetic changes, and how p53 and relative ncRNAs and mRNAs play roles in the process. In this study, workers from four arsenic plants and individuals who resided in villages far away from the four plants were recruited. Arsenic compounds, relative indices, 28 relative RNAs, and base modifications of exons 5-8 of p53 were detected separately. Several methods were used to analyze the associations between them. Results shown that As3MT RNA was closely associated with all selected lncRNAs, miRNAs, and mRNAs related to miRNA production and maturation, tumorigenesis, and base modifications of p53. There probably exists causal relationship. Base modifications of exons 7 and 8 of p53 had significant synergistic effects on the expression of As3MT RNA and a series of genetic indices. But miR-190, miR-548, and base modifications of exon 5 of p53 had substantial inhibitory effects. Arsenic compounds and relative indices of metabolic transformation may have limited roles. The main novel finding in the present study is that As3MT play special and significant roles in the genotoxicity and carcinogenesis which could be coordinated operation with p53, and influenced by epigenetic factors largely, such as lncRNAs and miRNAs. P53 and relative ncRNAs and mRNAs may regulate the process by interacting with As3MT. The changes may initiate by arsenic, but probability through indirect relationship.

Keywords: AS3MT; Arsenic; lncRNAs; miRNAs; p53.

MeSH terms

  • Arsenic* / metabolism
  • Arsenicals* / metabolism
  • DNA Methylation
  • Humans
  • Methyltransferases / genetics
  • Methyltransferases / metabolism
  • MicroRNAs* / metabolism
  • RNA, Long Noncoding* / genetics
  • RNA, Long Noncoding* / metabolism
  • RNA, Messenger / metabolism
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Arsenic
  • Tumor Suppressor Protein p53
  • RNA, Long Noncoding
  • Methyltransferases
  • Arsenicals
  • MicroRNAs
  • RNA, Messenger
  • AS3MT protein, human