Sex-Biased Expression of Pharmacogenes across Human Tissues

Biomolecules. 2021 Aug 13;11(8):1206. doi: 10.3390/biom11081206.

Abstract

Individual response to drugs is highly variable and largely influenced by genetic variants and gene-expression profiles. In addition, it has been shown that response to drugs is strongly sex-dependent, both in terms of efficacy and toxicity. To expand current knowledge on sex differences in the expression of genes relevant for drug response, we generated a catalogue of differentially expressed human transcripts encoded by 289 genes in 41 human tissues from 838 adult individuals of the Genotype-Tissue Expression project (GTEx, v8 release) and focused our analysis on relevant transcripts implicated in drug response. We detected significant sex-differentiated expression of 99 transcripts encoded by 59 genes in the tissues most relevant for human pharmacology (liver, lung, kidney, small intestine terminal ileum, skin not sun-exposed, and whole blood). Among them, as expected, we confirmed significant differences in the expression of transcripts encoded by the cytochromes in the liver, CYP2B6, CYP3A7, CYP3A5, and CYP1A1. Our systematic investigation on differences between male and female in the expression of drug response-related genes, reinforce the need to overcome the sex bias of clinical trials.

Keywords: drug metabolism; pharmacogenes; sex differences; sex-bias; transcripts.

MeSH terms

  • Cytochrome P-450 Enzyme System / metabolism*
  • Female
  • Humans
  • Male
  • Sex Factors
  • Transcriptome*

Substances

  • Cytochrome P-450 Enzyme System