Downregulated METTL14 Expression Correlates with Breast Cancer Tumor Grade and Molecular Classification

Biomed Res Int. 2020 Oct 20:2020:8823270. doi: 10.1155/2020/8823270. eCollection 2020.

Abstract

It is unclear whether the methyltransferase-like 14 (METTL14) protein promotes or suppresses cancer growth. We examined the association between METTL14 expression, cancer progression, and patient prognosis in a total of 398 breast cancer tissue specimens. Significantly fewer cancer tissue specimens compared with normal breast tissue expressed high levels of METTL14 (52.8% vs. 75.0%). METTL14 expression was negatively associated with tumor grade and positively associated with patient age, estrogen, and progesterone receptor status. High METTL14 expression was more common in luminal A and luminal B tissue (75.9% and 60.8%, respectively), compared with human epidermal growth factor receptor 2- (HER2-) enriched and triple-negative breast cancer (TNBC) samples (38.2% and 18.6%, respectively). In multiple logistic regression analysis, independent predictors of METTL14 expression in breast cancer included higher tumor grade (odds ratio (OR) = 0.494, 95% confidence interval (CI): 0.289-0.844; P = 0.010), TNBC subtype (OR = 0.109, 95% CI: 0.054-0.222; P < 0.001), and HER2-enriched subtype (OR = 0.298, 95% CI: 0.156-0.567; P < 0.001). No clear relationship was observed between patient prognosis and METTL14 expression. It appears that downregulated METTL14 expression in breast cancer is associated with tumor grade and molecular classification.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Breast Neoplasms / genetics*
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / mortality
  • Breast Neoplasms / pathology
  • Case-Control Studies
  • Female
  • Humans
  • Methyltransferases / genetics*
  • Methyltransferases / metabolism
  • Middle Aged
  • Neoplasm Grading
  • Neoplasm Staging
  • Receptor, ErbB-2 / deficiency
  • Receptor, ErbB-2 / genetics*
  • Receptors, Estrogen / deficiency
  • Receptors, Estrogen / genetics*
  • Receptors, Progesterone / deficiency
  • Receptors, Progesterone / genetics*
  • Receptors, Progesterone / metabolism
  • Survival Analysis
  • Triple Negative Breast Neoplasms / genetics*
  • Triple Negative Breast Neoplasms / metabolism
  • Triple Negative Breast Neoplasms / mortality
  • Triple Negative Breast Neoplasms / pathology

Substances

  • Receptors, Estrogen
  • Receptors, Progesterone
  • METTL14 protein, human
  • Methyltransferases
  • ERBB2 protein, human
  • Receptor, ErbB-2