SOX4: Epigenetic regulation and role in tumorigenesis

Hamza Hanieh*, Emad A. Ahmed, Radhakrishnan Vishnubalaji, Nehad M. Alajez

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

86 Citations (Scopus)

Abstract

Sex-determining region Y-related (SRY) high-mobility group box 4 (SOX4) is a member of the group C subfamily of SOX transcription factors and promotes tumorigenesis by endowing cancer cells with survival, migratory, and invasive capacities. Emerging evidence has highlighted an unequivocal role for this transcription factor in mediating various signaling pathways involved in tumorigenesis, epithelial-to-mesenchymal transition (EMT), and tumor progression. During the last decade, numerous studies have highlighted the epigenetic interplay between SOX4-targeting microRNAs (miRNAs), long noncoding RNAs (lncRNAs) and SOX4 and the subsequent modulation of tumorigenesis, invasion and metastasis. In this review, we summarize the current state of knowledge about the role of SOX4 in cancer development and progression, the epigenetic regulation of SOX4, and the potential utilization of SOX4 as a diagnostic and prognostic biomarker and its depletion as a therapeutic target.

Original languageEnglish
Pages (from-to)91-104
Number of pages14
JournalSeminars in Cancer Biology
Volume67
DOIs
Publication statusPublished - Dec 2020

Keywords

  • Cancer
  • EMT
  • Epigenetic regulation
  • SOX4
  • lncRNA
  • microRNA

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