CYP450 Gene Variations and Their Implications for Drug Response: A Pharmacogenomic Review

Authors

  • Anastasya Esther Fiorelina Siahaan Study Program of Pharmacy, Universitas Mulawarman, Samarinda, Indonesia Author
  • Juniza Firdha Suparningtyas Study Program of Pharmacy, Universitas Mulawarman, Samarinda, Indonesia Author https://orcid.org/0000-0002-3935-2412
  • Isti Faiza Sakinah Program Studi Farmasi, Fakultas Farmasi, Universitas Mulawarman Author
  • Khairani Tosuli Pharmacy Study Program, Faculty of Pharmacy, Mulawarman University Author
  • Ayla Azzura Pharmacy Study Program, Faculty of Pharmacy, Mulawarman University Author
  • Anastasya Esther Fiorelina Siahaan Pharmacy Study Program, Faculty of Pharmacy, Mulawarman University Author
  • ⁠Sabrina Pharmacy Study Program, Faculty of Pharmacy, Mulawarman University Author
  • ⁠Nanda Febriani Pharmacy Study Program, Faculty of Pharmacy, Mulawarman University Author
  • ⁠Maria Beatrix Ose Purek Study Program of Pharmacy, Universitas Mulawarman, Samarinda, Indonesia Author
  • Kaylila Aileen Pharmacy Study Program, Faculty of Pharmacy, Mulawarman University Author
  • Salwa Salsa Billa Pharmacy Study Program, Faculty of Pharmacy, Mulawarman University Author
  • Tasya Falda Puteri Pharmacy Study Program, Faculty of Pharmacy, Mulawarman University Author

DOI:

https://doi.org/10.30872/jtpc.v10i2.434

Keywords:

cytochrome P450, genetic variation, pharmacogenomic, phenoconversion, precision medicine

Abstract

The Human Genome Project (HGP) has significantly advanced our understanding of how human genetic variation affects drug response, particularly through metabolic enzymes such as Cytochrome P450 (CYP450). This study aimed to explore the impact of genetic variation on drug metabolism and its consequences for precision medicine therapies. This approach involved a literature review of various scientific articles discussing pharmacogenomics, CYP450 enzymes, and their clinical applications. The findings indicate that CYP450 enzymes are crucial in drug metabolism, especially during phase I reactions, such as oxidation, and their activity is heavily influenced by genetic polymorphisms, including those in CYP2C19. These genetic differences lead to variations in the ability of individuals to activate or eliminate drugs, thereby affecting the effectiveness of therapy and the likelihood of side effects. In addition to genetic factors, drug interactions, environmental influences, and the microbiome also play a role in drug response. For instance, genetic variation in the use of clopidogrel can result in therapeutic failure or a heightened risk of clinical events. Ultimately, integrating genomic data from the HGP with CYP450 enzyme profiles provides a vital basis for implementing precision medicine, allowing for more accurate drug and dosage selection, thereby enhancing therapeutic effectiveness and reducing the risk of side effects in patients.

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References

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Published

2026-07-31

How to Cite

CYP450 Gene Variations and Their Implications for Drug Response: A Pharmacogenomic Review. (2026). Journal of Tropical Pharmacy and Chemistry , 10(2), 73-79. https://doi.org/10.30872/jtpc.v10i2.434

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