State Key Laboratory of Cancer Biology, Cell Engineering Research Center & Department of Cell Biology, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Cancer Epidemiol Biomarkers Prev. 2012 Jan;21(1):217-27. doi: 10.1158/1055-9965.EPI-11-0624. Epub 2011 Oct 25.
Cumulative data have shown that microRNAs (miRNA) are involved in the etiology and prognosis of colorectal cancer (CRC). Genetic polymorphisms in pre-miRNA genes may influence the biogenesis and functions of their host miRNAs. However, whether these polymorphisms are associated with CRC prognosis remains unknown.
We analyzed the effects of seven single-nucleotide polymorphisms (SNP) in pre-miRNA genes on the prognosis of a Chinese population with 408 CRC patients with surgically-resected adenocarcinoma.
Two SNPs were identified to be significantly associated with recurrence-free survival and overall survival of the patients. The most significant SNP was rs6505162 in pre-miR-423. Compared with the homozygous wild-type genotype, the variant-containing genotypes of this SNP were significantly associated with both the overall survival (HR = 2.12, 95% CI = 1.34-3.34, P = 0.001) and the recurrence-free survival (HR = 1.59, 95% CI = 1.08-2.36, P = 0.019). Another SNP, rs4919510 in pre-miR-608, was also associated with altered recurrence-free survival (HR = 0.61, 95% CI = 0.41-0.92, P = 0.017). These effects were evident only in patients receiving chemotherapy but not in those without chemotherapy. In addition, the combined analysis of the two SNPs conferred a 2.84-fold (95% CI = 1.50-5.37, P = 0.001) increased risk of recurrence and/or death. Similarly, this effect was only prominent in those receiving chemotherapy (P < 0.001) but not in those without chemotherapy (P = 0.999).
Our data suggest that genetic polymorphisms in pre-miRNA genes may impact CRC prognosis especially in patients receiving chemotherapy, a finding that warrants further independent validation.
This is one of the first studies showing a prognostic role of pre-miRNA gene SNPs in CRC.
累积数据表明 microRNAs(miRNA)参与结直肠癌(CRC)的病因和预后。miRNA 前体基因的遗传多态性可能影响其宿主 miRNA 的生物发生和功能。然而,这些多态性是否与 CRC 预后相关尚不清楚。
我们分析了 7 个 miRNA 前体基因单核苷酸多态性(SNP)对 408 例接受手术切除腺癌的中国 CRC 患者预后的影响。
发现 2 个 SNP 与患者无复发生存和总生存显著相关。最显著的 SNP 是 pre-miR-423 中的 rs6505162。与纯合野生型基因型相比,该 SNP 的变异基因型与总生存(HR=2.12,95%CI=1.34-3.34,P=0.001)和无复发生存(HR=1.59,95%CI=1.08-2.36,P=0.019)均显著相关。另一个 SNP,pre-miR-608 中的 rs4919510,也与无复发生存的改变相关(HR=0.61,95%CI=0.41-0.92,P=0.017)。这些影响仅在接受化疗的患者中明显,而在未接受化疗的患者中不明显。此外,这两个 SNP 的联合分析显示复发和/或死亡的风险增加了 2.84 倍(95%CI=1.50-5.37,P=0.001)。同样,这种影响仅在接受化疗的患者中显著(P<0.001),而在未接受化疗的患者中不显著(P=0.999)。
我们的数据表明,miRNA 前体基因的遗传多态性可能影响 CRC 的预后,尤其是在接受化疗的患者中,这一发现需要进一步的独立验证。
这是第一项表明 pre-miRNA 基因 SNP 在 CRC 中具有预后作用的研究之一。