细胞色素1B1*3多态性与伊朗女性乳腺癌的关系

Faezeh Kholousi Adab, Z. T. Fard, M. Akbari
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引用次数: 4

摘要

背景:激素依赖性癌症,雌激素参与了乳腺癌的发展。CYP1B1属于P450酶超家族,参与雌激素的代谢。本研究探讨了伊朗妇女CYP1B1*3rs1056836多态性与癌症的关系。方法:对德黑兰Shaha-daye Tajrish医院收治的79名乳腺癌妇女和79名健康女性进行本病例对照研究。从所有参与者身上采集血样,提取他们的白细胞DNA。PCR-RFLP方法用于根据凝胶上碎片的大小对参与者进行基因分型。基于Hardy-Weinberg平衡模型,计算了等位基因的频率。结果:癌症组和对照组的平均年龄分别为48±8岁和43±6岁。计算基因型后,癌症组GG基因型、GC/CG基因型和CC基因型的百分比分别为30.38%、37.97%和31.65%,对照组GG型、GC/GG基因型、CC基因型分别为32.91%、53.16%和13.93%。根据Hardy-Weinberg平衡模型,癌症组G等位基因和C等位基因频率分别为49.37%和50.63,对照组分别为59.49%和40.51%。在CC纯合子方面,两组之间观察到统计学上的显著差异(P=0.008)。结论:研究结果表明,CYP1B1 rs1056836多态性与乳腺癌发生风险之间可能存在明显的相关性,因此多态性可能参与这种情况的发展。
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Association Between Cytochrome 1B1*3 Polymorphism and the Breast Cancer in a Group of Iranian Women
Background: Asahormone-dependentcancer,estrogenisinvolvedinthedevelopmentof breastcancer. CYP1B1 belongstotheP450 superfamily of enzymes and is involved in the metabolism of estrogen. The present study investigates the relationship between CYP1B1*3 rs1056836 polymorphism and breast cancer in Iranian women. Methods: Thepresentcase-controlstudywasconductedon79womenwithbreastcancerand79healthywomenadmittedtoShoha-daye Tajrish hospital in Tehran. Blood samples were taken from all the participants and their leukocyte DNA was extracted. The PCR-RFLP method was used for genotyping the participants based on the size of the pieces on the gel. Based on Hardy-Weinberg equilibrium model, the frequency of alleles was calculated. Results: The mean age of participants was 48 ± 8 years old in the cancer group and 43 ± 6 years old in the control group. After counting the genotypes, their percentages were calculated as 30.38% for the GG genotype, 37.97% for the GC/CG and 31.65% for the CC in the cancer group and as 32.91% for the GG genotype, 53.16% for the GC/CG and 13.93% for the CC in the control group. Based on Hardy-Weinberg equilibrium model, the frequency of the G allele and C allele was 49.37% and 50.63 in the cancer group, and about 59.49% and 40.51% in the control group. A statistically significant difference was observed between the two groups in terms of the CC homozygotes (P = 0.008). Conclusions: Theresultsobtainedshowedpossibilityof asignificantrelationshipbetween CYP1B1 rs1056836polymorphismandthe riskof developingbreastcancer,andthepolymorphismcan,therefore,besaidtobeinvolvedinthedevelopmentof thiscondition.
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