Association of rnasel and 8q24 variants with the presence and aggressiveness of hereditary and sporadic prostate cancer in a hispanic population
Autor: | Javier Cerda-Infante, Alejandro Godoy, Claudia Hurtado, Ignacio F. San Francisco, Susan V. Smalley, Viviana P. Montecinos, Pablo A. Rojas, Verónica Torres-Estay |
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Jazyk: | angličtina |
Rok vydání: | 2014 |
Předmět: |
Oncology
Male Risk medicine.medical_specialty Population Biology urologic and male genital diseases Genetic analysis Polymorphism Single Nucleotide polymorphism Prostate cancer Gene Frequency Internal medicine Genotype Endoribonucleases medicine Humans Genetic Predisposition to Disease Family history Chile education Allele frequency Genetic Association Studies Aged Gynecology education.field_of_study Case-control study RNASEL Gene Prostatic Neoplasms 8q24 Cell Biology Original Articles Sequence Analysis DNA Middle Aged medicine.disease prostate cancer Tumor Burden RNASEL Case-Control Studies Molecular Medicine Neoplasm Grading rs6983267 Chromosomes Human Pair 8 |
Zdroj: | JOURNAL OF CELLULAR AND MOLECULAR MEDICINE Artículos CONICYT CONICYT Chile instacron:CONICYT Journal of Cellular and Molecular Medicine |
Popis: | To study the association between the polymorphisms Arg462Gln and Asp541Glu from the RNASEL gene (1q25), and the polymorphisms rs620861, rs1447295, rs6983267, rs7837328 from the chromosome 8q24 with the risk of presenting prostate cancer (PCa) and its clinical characteristics in a Hispanic (Chilean) population. The study was performed on 21 control patients and 83 patients diagnosed with PCa. Polymorphisms were analysed from blood samples through real-time PCR by using TaqMan probes, and the genetic analysis was performed with the SNPStats program. Also, a comparison was performed between clinical characteristics of PCa and the presence of the different polymorphism genotypes by using the Minitab software. There was a significant association between the genotype G/G from the polymorphism rs6983267 with an overall increased risk of PCa, in patients both with or without family history of PCa (OR = 4.47, 95% CI = 1.05–18.94, P = 0.034 and OR = 3.57, 95% CI = 0.96–13.35, P = 0.037, respectively). Regarding clinical parameters, patients carrying the genotype C/C from the polymorphism Asp541Glu had significantly higher prostate-specific antigen (PSA) levels than patients carrying the other genotypes (P = 0.034). Moreover, patients with the genotype G/G of rs6983267 had higher PSA levels (P = 0.024). The polymorphism rs6983267 from region 3 of the chromosome 8q24 appears to be a prominent risk factor for PCa and a biomarker for cancer aggressiveness in the group of patients who presented higher levels of PSA at the time of diagnosis. |
Databáze: | OpenAIRE |
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