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Germline Allele-Specific Expression of TGFBR1 Confers an Increased Risk of Colorectal Cancer

机译:TGFBR1的种系等位基因特异性表达使结直肠癌的风险增加

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Much of the genetic predisposition to colorectal cancer (CRC) in humans is unexplained. Studying a Caucasian-dominated population in the United States, we showed that germline allele-specific expression (ASE) of the gene encoding transforming growth factor-p (TGF-β) type I receptor, TOFBR1, is a quantitative trait that occurs in 10 to 20% of CRC patients and 1 to 3% of controls. ASE results in reduced expression of the gene, is dominantly inherited, segregates in families, and occurs in sporadic CRC cases. Although subtle, the reduction in constitutive TGFBR1 expression alters SMAD-mediated TGF-β signaling. Two major TGFBR1 haplotypes are predominant among ASE cases, which suggests ancestral mutations, but causative germline changes have not been identified. Conservative estimates suggest that ASE confers a substantially increased risk of CRC (odds ratio, 8.7; 95% confidence interval, 2.6 to 29.1), but these estimates require confirmation and will probably show ethnic differences.
机译:人类对结直肠癌(CRC)的许多遗传易感性尚无法解释。在美国研究了一个以白种人为主的人群,我们发现编码转化生长因子-p(TGF-β)I型受体TOFBR1的基因的种系等位基因特异性表达(ASE)是一种定量特征,发生于10 20%的CRC患者和1-3%的对照。 ASE导致基因表达降低,主要遗传,在家族中分离,并在偶发的CRC病例中发生。尽管很微妙,但组成型TGFBR1表达的减少改变了SMAD介导的TGF-β信号传导。在ASE病例中,主要存在两种主要的TGFBR1单倍型,这表明祖先发生了突变,但尚未鉴定出引起种系变化的原因。保守的估计表明,ASE会大大增加患CRC的风险(优势比为8.7; 95%的置信区间为2.6至29.1),但是这些估计需要确认,并且可能显示出种族差异。

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