Fores-Martos Jaume, Cervera-Vidal Raimundo, Sierra-Roca Julia, Lozano-Asencio Carlos, Fedele Vita, Cornelissen Sten, Edvarsen Hege, Tadeo-Cervera Irene, Eroles Pilar, Lluch Ana, Tabares-Seisdedos Rafa, Falcó Antonio, Van't Veer Laura J, Schmidt Marjanka, Quigley David A, Børresen-Dale Anne-Lise, Kristensen Vessela N, Balmain Allan, Climent Joan
ESI International Chair at CEU-UCH, CEU Universities, Valencia, Spain.
Biomedical Research Networking Center of Mental Health (CIBERSAM), Madrid, Spain.
NPJ Breast Cancer. 2021 Sep 10;7(1):118. doi: 10.1038/s41523-021-00329-2.
Polymorphisms in the PER3 gene have been associated with several human disease phenotypes, including sleep disorders and cancer. In particular, the long allele of a variable number of tandem repeat (VNTR) polymorphism has been previously linked to an increased risk of breast cancer. Here we carried out a combined germline and somatic genetic analysis of the role of the PER3 polymorphism in breast cancer. The combined data from 8284 individuals showed a non-significant trend towards increased breast cancer risk in the 5-repeat allele homozygous carriers (OR = 1.17, 95% CI: 0.97-1.42). We observed allelic imbalance at the PER3 locus in matched blood and tumor DNA samples, showing a significant retention of the long variant (risk) allele in tumor samples, and a preferential loss of the short repetition allele (p = 0.0005). Gene co-expression analysis in healthy and tumoral breast tissue samples uncovered significant associations between PER3 expression levels with those from genes which belong to several cancer-associated pathways. Finally, relapse-free survival (RFS) analysis showed that low expression levels of PER3 were linked to a significant lower RSF in luminal A (p = 3 × 10) but not in the rest of breast cancer subtypes.
PER3基因的多态性与多种人类疾病表型相关,包括睡眠障碍和癌症。特别是,可变数目串联重复序列(VNTR)多态性的长等位基因先前已与乳腺癌风险增加相关。在此,我们对PER3多态性在乳腺癌中的作用进行了种系和体细胞联合基因分析。来自8284名个体的综合数据显示,5重复等位基因纯合携带者患乳腺癌风险增加的趋势不显著(OR = 1.17,95% CI:0.97 - 1.42)。我们在匹配的血液和肿瘤DNA样本中观察到PER3基因座的等位基因失衡,显示肿瘤样本中长变异(风险)等位基因显著保留,而短重复等位基因优先丢失(p = 0.0005)。健康和肿瘤乳腺组织样本中的基因共表达分析揭示了PER3表达水平与属于几种癌症相关途径的基因表达水平之间存在显著关联。最后,无复发生存期(RFS)分析表明,PER3低表达水平与腔面A型乳腺癌患者的RFS显著降低相关(p = 3×10),但在其他乳腺癌亚型中并非如此。