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Single nucleotide polymorphisms in both endometriosis and ovarian cancer

机译:子宫内膜异位症和卵巢癌的单核苷酸多态性

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摘要

Sir We read with interest the recent article by Heidemann et al. which reviewed the relationship between endometriosis and ovarian cancer in the literature (1). Heidemann et al. (1) concluded that women with endometriosis have an increased risk of developing clear-cell and endometrioid ovarian cancer subtypes. This review highlights the importance of providing follow-up care to endometriosis patients. Heinemann et al. commented on the importance of genotyping (1). Genotyping is the process of determining differences in the genetic make-up of individuals using biologic methods. Single nucleotide polymorphisms (SNPs), DNA sequence variation in single nucleotides (A, T, G and C) within a gene, are a well known and a commonly used method to investigate genetic differences. Because polymorphisms can affect the function of genes and disease, genetic polymorphisms are a useful method for the prediction and prevention of disease. Preliminary data from our laboratory concerning gene polymorphisms in endometriosis indicate that the MUC4 and ER genes may be linked to endometriosis and we wanted to determine common genetic factors between endometriosis and ovarian cancer (2). Specific keyword searches of the electronic database PubMed (The National Center for Biotechnology Information; NCBI) were used to identify additional polymorphisms and SNPs potentially involved in the relation between endometriosis and ovarian cancer.
机译:爵士我们感兴趣地阅读了Heidemann等人的最新文章。该文献综述了子宫内膜异位症与卵巢癌之间的关系(1)。 Heidemann等。 (1)得出结论,患有子宫内膜异位症的女性患透明细胞和子宫内膜样卵巢癌亚型的风险增加。这篇综述强调了为子宫内膜异位症患者提供后续护理的重要性。 Heinemann等。评论了基因分型的重要性(1)。基因分型是使用生物学方法确定个体遗传组成差异的过程。单核苷酸多态性(SNP),即基因内单核苷酸(A,T,G和C)中DNA序列的变化,是研究遗传差异的众所周知且常用的方法。由于多态性会影响基因和疾病的功能,因此遗传多态性是预测和预防疾病的有用方法。来自我们实验室的有关子宫内膜异位症中基因多态性的初步数据表明,MUC4和ER基因可能与子宫内膜异位症相关,我们希望确定子宫内膜异位症和卵巢癌之间的常见遗传因素(2)。使用电子数据库PubMed(美国国家生物技术信息中心; NCBI)的特定关键字搜索来识别可能与子宫内膜异位症和卵巢癌之间的关系有关的其他多态性和SNP。

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