Catalano Calogerina, da Silva Filho Miguel I, Jiraskova Katerina, Vymetalkova Veronika, Levy Miroslav, Liska Vaclav, Vycital Ondrej, Naccarati Alessio, Vodickova Ludmila, Hemminki Kari, Vodicka Pavel, Weber Alexander N R, Försti Asta
Division of Molecular Genetic Epidemiology, German Cancer Research Center (DKFZ), Heidelberg.
Department of Molecular Biology of Cancer, Institute of Experimental Medicine of the Czech Academy of Sciences.
Eur J Gastroenterol Hepatol. 2018 Aug;30(8):838-842. doi: 10.1097/MEG.0000000000001154.
NLRC5 is an interferon γ-inducible protein, which plays a role in immune surveillance with a potential influence on cancer survival.
We aimed to evaluate the effect of potential regulatory variants in NLRC5 on overall survival and survival after 5-fluorouracil (5-FU)-based therapy of colorectal cancer (CRC) patients.
We carried out a case-only study in a Czech population of 589 cases; 232 received 5-FU-based therapy. Eleven variants within NLRC5 were selected using in-silico tools. Associations between polymorphisms and survival were assessed by Cox regression analysis adjusting for age at diagnosis, sex, and TNM stage. Survival curves were derived using the Kaplan-Meier method.
Two variants showed a significant association with survival. All patients and metastasis-free patients at the time of diagnosis (pM0) who were homozygous carriers of the minor allele of rs27194 had a decreased overall survival (OSall and OSpM0) and event-free survival (EFSpM0) under a recessive model (OSall P=0.003, OSpM0 P=0.005, EFSpM0 P=0.01, respectively). OS was also decreased for all patients and for pM0 patients who carried at least one minor allele of rs289747 (OSall P=0.03 and OSpM0 P=0.003, respectively). Among CRC patients, who underwent a 5-FU-based adjuvant regimen, rs12445252 was associated with OSall, OSpM0 and EFSpM0, according to the dosage of the minor allele T (OSall P=0.0004, OSpM0 P=0.0001, EFSpM0 P=0.008, respectively).
Our results showed that polymorphisms in NLRC5 may be used as prognostic markers of survival of CRC patients, as well as for survival in response to 5-FU treatment.
NLRC5是一种γ干扰素诱导蛋白,在免疫监视中发挥作用,可能对癌症生存产生影响。
我们旨在评估NLRC5中潜在调控变异对结直肠癌(CRC)患者总生存期及基于5-氟尿嘧啶(5-FU)治疗后的生存期的影响。
我们在捷克的589例患者群体中开展了一项病例对照研究;其中232例接受了基于5-FU的治疗。使用计算机模拟工具选择了NLRC5基因内的11个变异。通过Cox回归分析评估多态性与生存期之间的关联,并对诊断时的年龄、性别和TNM分期进行校正。采用Kaplan-Meier法绘制生存曲线。
两个变异与生存期显著相关。rs27194次要等位基因的纯合携带者,在隐性模型下,所有患者以及诊断时无转移患者(pM0)的总生存期(OSall和OSpM0)和无事件生存期(EFSpM0)均降低(OSall P = 0.003,OSpM0 P = 0.005,EFSpM0 P = 0.01)。携带rs289747至少一个次要等位基因的所有患者和pM0患者的总生存期也降低(分别为OSall P = 0.03和OSpM0 P = 0.003)。在接受基于5-FU辅助治疗方案的CRC患者中,根据次要等位基因T的剂量,rs12445252与OSall、OSpM0和EFSpM0相关(分别为OSall P = 0.0004,OSpM0 P = 0.0001,EFSpM0 P = 0.008)。
我们的结果表明,NLRC5中的多态性可作为CRC患者生存以及对5-FU治疗反应的预后标志物。