TSPYL Family Regulates CYP17A1 and CYP3A4 Expression: Potential Mechanism Contributing to Abiraterone Response in Metastatic Castration-Resistant Prostate Cancer

Clin Pharmacol Ther. 2018 Jul;104(1):201-210. doi: 10.1002/cpt.907. Epub 2017 Nov 22.

Abstract

The testis-specific Y-encoded-like protein (TSPYL) gene family includes TSPYL1 to TSPYL6. We previously reported that TSPYL5 regulates cytochrome P450 (CYP) 19A1 expression. Here we show that TSPYLs, especially TSPYL 1, 2, and 4, can regulate the expression of many CYP genes, including CYP17A1, a key enzyme in androgen biosynthesis, and CYP3A4, an enzyme that catalyzes the metabolism of abiraterone, a CYP17 inhibitor. Furthermore, a common TSPYL1 single nucleotide polymorphism (SNP), rs3828743 (G/A) (Pro62Ser), abolishes TSPYL1's ability to suppress CYP3A4 expression, resulting in reduced abiraterone concentrations and increased cell proliferation. Data from a prospective clinical trial of 87 metastatic castration-resistant prostate cancer patients treated with abiraterone acetate/prednisone showed that the variant SNP genotype (A) was significantly associated with worse response and progression-free survival. In summary, TSPYL genes are novel CYP gene transcription regulators, and genetic alteration within these genes significantly influences response to drug therapy through transcriptional regulation of CYP450 genes.

Trial registration: ClinicalTrials.gov NCT01953640.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Abiraterone Acetate / pharmacology
  • Abiraterone Acetate / therapeutic use*
  • Cell Cycle Proteins / drug effects
  • Cell Cycle Proteins / genetics
  • Cell Proliferation / drug effects
  • Cell Proliferation / genetics
  • Cytochrome P-450 CYP3A / drug effects
  • Cytochrome P-450 CYP3A / genetics*
  • Cytochrome P-450 CYP3A / metabolism
  • Cytochrome P-450 Enzyme Inhibitors / pharmacology
  • Cytochrome P-450 Enzyme Inhibitors / therapeutic use*
  • DNA-Binding Proteins
  • Dehydroepiandrosterone / metabolism
  • Gene Expression Regulation / drug effects
  • Gene Knockdown Techniques
  • Hep G2 Cells
  • Humans
  • Male
  • Neoplasm Metastasis
  • Nuclear Proteins / drug effects
  • Nuclear Proteins / genetics
  • Proportional Hazards Models
  • Prostatic Neoplasms, Castration-Resistant / drug therapy*
  • Prostatic Neoplasms, Castration-Resistant / pathology
  • RNA, Messenger / metabolism
  • Steroid 17-alpha-Hydroxylase / antagonists & inhibitors
  • Steroid 17-alpha-Hydroxylase / drug effects
  • Steroid 17-alpha-Hydroxylase / genetics*
  • Treatment Outcome

Substances

  • Cell Cycle Proteins
  • Cytochrome P-450 Enzyme Inhibitors
  • DNA-Binding Proteins
  • Nuclear Proteins
  • RNA, Messenger
  • TSPY1 protein, human
  • TSPY4 protein, human
  • TSPYL2 protein, human
  • TSPYL5 protein, human
  • Dehydroepiandrosterone
  • Cytochrome P-450 CYP3A
  • CYP17A1 protein, human
  • Steroid 17-alpha-Hydroxylase
  • Abiraterone Acetate

Associated data

  • ClinicalTrials.gov/NCT01953640