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dc.contributor.author | De La Cruz, Angelica | |
dc.contributor.author | MEJIA SANCHEZ, FERNANDO | |
dc.contributor.author | Hernández Serrano, Maricela | |
dc.contributor.author | Montenegro Morales, Laura Patricia | |
dc.contributor.author | CASTILLO CADENA, JULIETA | |
dc.creator | De La Cruz, Angelica;#0000-0003-4347-6079 | |
dc.creator | MEJIA SANCHEZ, FERNANDO; 506806 | |
dc.creator | Hernández Serrano, Maricela;x1349783 | |
dc.creator | Montenegro Morales, Laura Patricia;x1340620 | |
dc.creator | CASTILLO CADENA, JULIETA; 202796 | |
dc.date.accessioned | 2020-02-07T20:26:47Z | |
dc.date.available | 2020-02-07T20:26:47Z | |
dc.date.issued | 2019-06-12 | |
dc.identifier.issn | 0970-938X | |
dc.identifier.uri | http://hdl.handle.net/20.500.11799/105538 | |
dc.description | The CYP3A4*2 polymorphism is rare in the population studied. Given the low frequency of CYP3A4*2 polymorphisms found in homozygous or heterozygous condition, it is advisable to consider the genotype of the patient before prescribing drugs metabolized by this gene. | es |
dc.description.abstract | Variability in response to drugs is a problem in clinical practice. The rate of patients who respond adequately to pharmacological therapy is generally around 60. The CYP450 multienzyme complex is a microsomal system located in the endoplasmic reticulum. The enzymes participate in phase I metabolism of xenobiotics. CYP3A4 is the isoenzyme mostly expressed in liver. Its gene is polymorphic, of which CYP3A4*1A is the wild allele and CYP3A4*2 is a polymorphism which consists of the S222P substitution in the amino acid sequence, affecting the activity of the enzyme. Methods: In this study, we determine the frequency of CYP3A4*2 polymorphism in Mexican individuals. 62 apparently healthy individuals, from Toluca de Lerdo, Mexico. The sample was 3 mL of peripheral blood. The DNA was extracted and PCR-RFLPs were performed. Results:58 individuals possess the wild allele in homozygosity CYP3A4*1A/CYP3A4*1A (94%) and 4 individuals were heterozygous CYP3A4*1A/CYP3A4*2 (6%). The homozygous polymorphic CYP3A4*2/CYP3A4*2 was not found in any individual. | es |
dc.description.sponsorship | COMECYT | es |
dc.language.iso | eng | es |
dc.publisher | Biomedical Research | es |
dc.rights | openAccess | es |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0 | |
dc.subject | Research Subject Categories | es |
dc.subject | Research Subject Categories | es |
dc.subject.classification | MEDICINA Y CIENCIAS DE LA SALUD | |
dc.title | Importance of the identification of the CYP3A4*2 polymorphism for the prescription of pharmacological treatment | es |
dc.type | Artículo | es |
dc.provenance | Científica | es |
dc.road | Dorada | es |
dc.organismo | Química | es |
dc.ambito | Internacional | es |
dc.audience | students | es |
dc.audience | researchers | es |
dc.type.conacyt | article | |
dc.identificator | 3 | |
dc.relation.vol | 30 |