Siraj Abdul K, Khalak Hanif G, Sultana Mehar, Al-Rasheed Maha, Bavi Prashant, Al-Sanea Nasser, Al-Dayel Fouad, Uddin Shahab, Alkuraya Fowzan S, Al-Kuraya Khawla S
Human Cancer Genomic Research, Research Centre, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
Genet Med. 2013;14(8):720-728. doi: 10.1038/gim.2012.27. Epub 2012 Apr 5.
Purpose:Runs of homozygosity (ROHs) represent a measure of the extent of autozygosity and are correlated with the extent of inbreeding. Recently, it has been suggested that ROHs may contribute to the risk of colorectal cancer (CRC). The high rate of consanguinity and CRC in the Saudi population prompted us to test the role of autozygosity in the CRC risk.Methods:We compared 48 Saudi CRC patients to 100 ethnically matched controls, processed on the Affymetrix 250K StyI SNP GeneChip platform and analyzed using the plink package.Results:We could find no evidence of a significant relationship between autozygosity and CRC risk.Conclusion:The negative results in our study add additional significance to what has been previously reported in literature, as this is the first study to address these questions in an inbred population. Our subgroup analysis of patients with microsatellite unstable-positive tumors as compared with other groups did not significantly change our results. Although these results do not rule out the presence of recessively acting CRC-predisposing genes in a small percentage of patients, which our relatively small sample size could not capture, they suggest that such genes are unlikely to account for the disturbingly high incidence of CRC in our consanguineous population.Genet Med advance online publication 5 April 2012.
纯合子连续片段(ROHs)是衡量自体同源性程度的指标,与近亲繁殖程度相关。最近,有人提出ROHs可能与结直肠癌(CRC)风险有关。沙特人群中较高的近亲结婚率和CRC发病率促使我们研究自体同源性在CRC风险中的作用。
我们将48例沙特CRC患者与100例种族匹配的对照进行比较,在Affymetrix 250K StyI SNP基因芯片平台上进行处理,并使用plink软件包进行分析。
我们未发现自体同源性与CRC风险之间存在显著关系的证据。
我们研究中的阴性结果为先前文献报道增添了更多意义,因为这是第一项在近亲繁殖人群中探讨这些问题的研究。与其他组相比,我们对微卫星不稳定阳性肿瘤患者的亚组分析并未显著改变我们的结果。尽管这些结果不能排除在一小部分患者中存在隐性作用的CRC易感基因(我们相对较小的样本量可能未捕捉到),但它们表明此类基因不太可能是导致我们近亲繁殖人群中CRC发病率高得惊人的原因。《遗传医学》2012年4月5日在线优先发表。