UGT1A1 regulatory variant with potential effect on efficacy of HIV and cancer drugs commonly prescribed in South Africa.
Jenny Mary MathewPhelelani Thokozani MpangaseDhriti SenguptaStanford KwandaDemetra Mavri-DamelinMichelle RamsayPublished in: Pharmacogenomics (2021)
Aim: Despite the high disease burden of human immunodeficiency virus (HIV) infection and colorectal cancer (CRC) in South Africa (SA), treatment-relevant pharmacogenetic variants are understudied. Materials & methods: Using publicly available genotype and gene expression data, a bioinformatic pipeline was developed to identify liver expression quantitative trait loci (eQTLs). Results: A novel cis-eQTL, rs28967009, was identified for UGT1A1, which is predicted to upregulate UGT1A1 expression thereby potentially affecting the metabolism of dolutegravir and irinotecan, which are extensively prescribed in SA for HIV and colorectal cancer treatment, respectively. Conclusion: As increased UGT1A1 expression could affect the clinical outcome of dolutegravir and irinotecan treatment by increasing drug clearance, patients with the rs28967009A variant may require increased drug doses to reach therapeutic levels or should be prescribed alternative drugs.
Keyphrases
- antiretroviral therapy
- human immunodeficiency virus
- hiv positive
- hiv infected
- south africa
- hiv infected patients
- poor prognosis
- gene expression
- hepatitis c virus
- hiv aids
- men who have sex with men
- hiv testing
- dna methylation
- multidrug resistant
- transcription factor
- long non coding rna
- emergency department
- climate change
- genome wide
- drug induced
- risk factors
- big data
- combination therapy
- young adults
- squamous cell carcinoma
- deep learning