Multi-omic analyses of m5C readers reveal their characteristics and immunotherapeutic proficiency

Rui Xu1, Yue Wang2, Ye Kuang3

  • 1Department of Development Planning, International Medical Opening-up Pilot Zone (China), Fangchenggang, Guangxi Province, China.

Scientific Reports
|January 18, 2024
PubMed

Insights

This study analyzes 5-methylcytosine (m5C) readers ALYREF and YBX1 in cancer. Their expression correlates with prognosis and tumor microenvironment, suggesting potential therapeutic targets.

Area of Science:

  • Oncology
  • Molecular Biology
  • Epigenetics

Background:

  • 5-methylcytosine (m5C) is a key RNA modification.
  • m5C readers, like ALYREF and YBX1, are crucial for m5C recognition.
  • Their comprehensive roles in pan-cancer remain underexplored.

Purpose of the Study:

  • To investigate the expression, prognostic value, and molecular functions of ALYREF and YBX1 across various cancers.
  • To explore the association of ALYREF and YBX1 with the tumor microenvironment, immune landscape, and drug resistance.
  • To elucidate the relationship between ALYREF, YBX1, eukaryotic initiation factors (eIFs), and mRNA dynamics.

Main Methods:

  • Utilized TCGA and GTEx databases for expression and prognostic analyses.
  • Assessed tumor microenvironment, immune checkpoints, immunomodulators, TIDE score, and drug resistance.
  • Performed GO, KEGG, and GSEA analyses for functional enrichment.

Main Results:

  • ALYREF and YBX1 showed aberrant expression, positively associated with prognosis in KIRP, LGG, and LIHC.
  • Expression levels correlated significantly with tumor immune infiltration and immune modulators.
  • Established correlations between ALYREF, YBX1, eIFs, and mRNA dynamics.

Conclusions:

  • ALYREF and YBX1 play significant roles in cancer, influencing prognosis and the tumor immune microenvironment.
  • Findings highlight the intricate interplay between m5C readers, eIFs, and mRNA processing.
  • Suggests potential for combined modality therapy involving m5C readers for improved cancer treatment.

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