Molecular insight into histone methylation as a novel target for oral squamous cell carcinoma: future hope in

Peramaiyan Rajendran1, Monisha Prasad2, Enas M Ali1

  • 1Department of Biological Sciences, College of Science, King Faisal University, Al-Ahsa, 31982, Saudi Arabia.

Journal of Cancer
|February 24, 2025
PubMed

Insights

Histone methylation, a key regulator of gene expression, is crucial for understanding oral squamous cell carcinoma (OSCC). Further research into histone methylation targets may improve OSCC treatment and prognosis.

Area of Science:

  • Oncology
  • Molecular Biology
  • Epigenetics

Background:

  • Oral squamous cell carcinoma (OSCC) is a prevalent malignancy with significant treatment challenges, including drug resistance, invasion, and migration.
  • Understanding the genetic and epigenetic factors driving oral carcinogenesis is complex due to varied clinic-pathological parameters.
  • Histone modifications, particularly methylation, play a critical role in regulating gene expression, cell development, and differentiation.

Purpose of the Study:

  • To review the dysregulated histone methylation patterns and associated enzymes in oral squamous cell carcinoma (OSCC).
  • To investigate the role of lysine methylation in OSCC cell migration, chemo-resistance, and invasion.
  • To highlight the potential of histone methylation as a therapeutic target for OSCC.

Main Methods:

  • Literature review focusing on histone methylation and its modifying enzymes in the context of OSCC.
  • Analysis of existing research on the impact of histone methylation on gene regulation, cell processes, and therapeutic resistance in OSCC.
  • Examination of the specific role of lysine methylation in OSCC progression and invasion.

Main Results:

  • Dysregulated histone methylation and its modifying enzymes are linked to the development and etiology of OSCC.
  • Histone methylation significantly influences gene expression, affecting cell development and differentiation in oral cancer.
  • Lysine methylation is implicated in promoting OSCC cell migration, invasion, and chemo-resistance.

Conclusions:

  • Histone methylation is a critical epigenetic mechanism involved in OSCC pathogenesis.
  • Targeting histone methylation pathways presents a promising strategy for improving early detection, prognostic prediction, and therapeutic outcomes in OSCC.
  • Further investigation into histone methylation as a therapeutic target is warranted for effective OSCC treatment.

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