Lemos Manuel C, Carrilho Francisco, Rodrigues Fernando, Coutinho Eduarda, Gomes Leonor, Carvalheiro Manuela, Regateiro Fernando J
Centro de Investigação em Ciências da Saúde (CICS), Faculdade de Ciências da Saúde, Universidade da Beira Interior, 6200-506 Covilhã, Portugal.
Clin Endocrinol (Oxf). 2007 Aug;67(2):180-3. doi: 10.1111/j.1365-2265.2007.02858.x. Epub 2007 Jun 4.
Xenobiotic-metabolizing enzymes are widely polymorphic and confer interindividual variation in the ability to detoxify carcinogens or to activate pro-carcinogens. A common polymorphism of cytochrome P450 2D6 (CYP2D6) results in lack of enzyme activity and has been associated with an altered susceptibility to several cancers. The aim of this study was to investigate the association between the CYP2D6 poor metaboliser genotype and the risk of papillary thyroid cancer (PTC).
Retrospective case-control study.
One hundred and eighty-seven patients with PTC and 256 controls.
Genotyping was performed by PCR and restriction enzyme analysis to detect the presence of the common CYP2D6*4 poor metaboliser allele.
The frequency of individuals with the homozygous poor metaboliser genotype was lower in the patient group [1.6 vs. 5.5%, P = 0.037, OR = 0.28 (95% CI 0.09-0.93)]. The CYP2D6*4 allele frequency was also lower in the patient group [13.4 vs. 21.7%, P = 0.002, OR = 0.56 (95% CI 0.39-0.80)].
The results suggest that the poor metaboliser genotype is associated with a protective effect against PTC. This could be explained by a possible role of CYP2D6 on the metabolic activation of putative environmental chemical thyroid carcinogens or by linkage to another cancer-causing gene. Further research may allow the identification of metabolic risk factors and contribute towards understanding the molecular mechanisms involved in thyroid carcinogenesis.
异生物素代谢酶具有广泛的多态性,会导致个体在解毒致癌物或激活前致癌物的能力上存在差异。细胞色素P450 2D6(CYP2D6)的一种常见多态性会导致酶活性缺乏,并与几种癌症易感性的改变有关。本研究的目的是调查CYP2D6慢代谢基因型与甲状腺乳头状癌(PTC)风险之间的关联。
回顾性病例对照研究。
187例PTC患者和256例对照。
采用聚合酶链反应(PCR)和限制性酶切分析进行基因分型,以检测常见的CYP2D6*4慢代谢等位基因的存在。
患者组中纯合慢代谢基因型个体的频率较低[1.6%对5.5%,P = 0.037,比值比(OR)= 0.28(95%可信区间0.09 - 0.93)]。患者组中CYP2D6*4等位基因频率也较低[13.4%对21.7%,P = 0.002,OR = 0.56(95%可信区间0.39 - 0.80)]。
结果表明慢代谢基因型与PTC的保护作用相关。这可能是由于CYP2D6在假定的环境化学甲状腺致癌物的代谢激活中可能发挥的作用,或者是与另一个致癌基因的连锁关系。进一步的研究可能有助于识别代谢风险因素,并有助于理解甲状腺癌发生的分子机制。