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短文:调节性NLRC5变体对结直肠癌生存及基于5-氟尿嘧啶化疗的影响

Short article: Influence of regulatory NLRC5 variants on colorectal cancer survival and 5-fluorouracil-based chemotherapy.

作者信息

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

机构信息

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.

出版信息

Eur J Gastroenterol Hepatol. 2018 Aug;30(8):838-842. doi: 10.1097/MEG.0000000000001154.

Abstract

BACKGROUND

NLRC5 is an interferon γ-inducible protein, which plays a role in immune surveillance with a potential influence on cancer survival.

OBJECTIVE

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.

PATIENTS AND METHODS

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.

RESULTS

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).

CONCLUSION

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.

摘要

背景

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。

目的

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。

患者与方法

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。

结果

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)。

结论

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。

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