Garcia-Etxebarria Koldo, Clos-Garcia Marc, Telleria Oiana, Nafría Beatriz, Alonso Cristina, Iruarrizaga-Lejarreta Marta, Franke Andre, Crespo Anais, Iglesias Agueda, Cubiella Joaquín, Bujanda Luis, Falcón-Pérez Juan Manuel
Grupo de Genética Gastrointestinal, Biodonostia, 20014 San Sebastián, Spain.
Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), 08036 Barcelona, Spain.
Cancers (Basel). 2021 Dec 10;13(24):6216. doi: 10.3390/cancers13246216.
Colorectal cancer (CRC), a major health concern, is developed depending on environmental, genetic and microbial factors. The microbiome and metabolome have been analyzed to study their role in CRC. However, the interplay of host genetics with those layers in CRC remains unclear.
120 individuals were sequenced and association analyses were carried out for adenoma and CRC risk, and for selected components of the microbiome and metabolome. The epistasis between genes located in cholesterol pathways was analyzed; modifiable risk factors were studied using Mendelian randomization; and the three omic layers were used to integrate their data and to build risk prediction models.
We detected genetic variants that were associated to components of metabolome or microbiome and adenoma or CRC risk (e.g., in , and genes). In addition, we found interactions between genes of cholesterol metabolism, and HDL cholesterol levels affected adenoma ( = 0.0448) and CRC ( = 0.0148) risk. The combination of the three omic layers to build risk prediction models reached high AUC values (>0.91).
The use of the three omic layers allowed for the finding of biological mechanisms related to the development of adenoma and CRC, and each layer provided complementary information to build risk prediction models.
结直肠癌(CRC)是一个主要的健康问题,其发生取决于环境、遗传和微生物因素。已对微生物组和代谢组进行分析以研究它们在结直肠癌中的作用。然而,宿主遗传学与结直肠癌中这些层面之间的相互作用仍不清楚。
对120名个体进行测序,并对腺瘤和结直肠癌风险以及微生物组和代谢组的选定成分进行关联分析。分析了位于胆固醇途径中的基因之间的上位性;使用孟德尔随机化研究了可改变的风险因素;并利用这三个组学层面整合数据并建立风险预测模型。
我们检测到与代谢组或微生物组成分以及腺瘤或结直肠癌风险相关的基因变异(例如,在 、 和 基因中)。此外,我们发现胆固醇代谢基因之间存在相互作用,高密度脂蛋白胆固醇水平影响腺瘤( = 0.0448)和结直肠癌( = 0.0148)风险。结合三个组学层面建立风险预测模型达到了较高的AUC值(>0.91)。
使用这三个组学层面有助于发现与腺瘤和结直肠癌发生相关的生物学机制,并且每个层面都为建立风险预测模型提供了互补信息。