首页> 外文OA文献 >Interleukins as new prognostic genetic biomarkers in non-small cell lung cancer
【2h】

Interleukins as new prognostic genetic biomarkers in non-small cell lung cancer

机译:白介素在非小细胞肺癌中作为新的预后遗传生物标志物

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

Background: Surgery is the standard treatment for early-stage NSCLC, and platinum-based chemotherapy remains as the treatment of choice for advanced-stage NSCLC patients with naïve EGFR status. However, overall 5-years relative survival rates are low. Interleukins (ILs) are crucial for processes associated with tumor development. In NSCLC, IL1B, IL6, IL12A, IL13 and IL16 gene polymorphisms may contribute to individual variation in terms of patient survival. The purpose of this study was to evaluate the association between IL gene polymorphisms and survival in NSCLC patients.Methods: A prospective cohorts study was performed, including 170 NSCLC patients (114 Stage IIIB-IV, 56 Stage I-IIIA). IL1B (C > T; rs1143634), IL1B (C > T; rs12621220), IL1B (C > G; rs1143623), IL1B (A > G; rs16944), IL1B (C > T; rs1143627), IL6 (C > G; rs1800795), IL12A (C > T; rs662959), IL13 (A > C; rs1881457) and IL16 (G > T; rs7170924) gene polymorphisms were analyzed by PCR Real-Time.Results: Patients with IL16 rs7170924-GG genotype were in higher risk of death (p = 0.0139; HR = 1.82; CI95% = 1.13–2.94) Furthermore, carriers of the TT genotype for IL12A rs662959 presented higher risk of progression in the non-resected NSCLC patient subgroup (p = 0.0412; HR = 4.49; CI95% = 1.06–18.99). The rest of polymorphisms showed no effect of on outcomes.Conclusions: Our results suggest that IL16 rs7170924-GG and IL12A rs662959-TT genotypes predict higher risk of death and progression, respectively, in NSCLC patients. No influence of IL1B rs12621220, IL1B rs1143623, IL1B rs16944, IL1B rs1143627, IL6 rs1800795, IL13 rs1881457 on NSCLC clinical outcomes was found in our patients.
机译:背景:外科手术是早期NSCLC的标准治疗方法,铂类化学疗法仍是未曾有EGFR状态的晚期NSCLC患者的治疗选择。但是,总体5年相对生存率很低。白介素(ILs)对于与肿瘤发展相关的过程至关重要。在NSCLC中,IL1B,IL6,IL12A,IL13和IL16基因多态性可能会导致患者生存方面的个体差异。方法:一项前瞻性队列研究包括170名NSCLC患者(114例IIIB-IV期,56例I-IIIA期)。 IL1B(C> T; rs1143634),IL1B(C> T; rs12621220),IL1B(C> G; rs1143623),IL1B(A> G; rs16944),IL1B(C> T; rs1143627),IL6(C> G PCR实时分析了IL12A(C> T; rs662959),IL13(A> C; rs1881457)和IL16(G> T; rs7170924)基因多态性。结果:IL16 rs7170924-GG基因型的患者死亡风险较高(p = 0.0139; HR = 1.82; CI95%= 1.13–2.94)。此外,IL12A rs662959 TT基因型携带者在未切除的NSCLC患者亚组中具有较高的进展风险(p = 0.0412; HR) = 4.49; CI95%= 1.06-18.99)。结论:我们的结果表明,IL16 rs7170924-GG和IL12A rs662959-TT基因型分别预测NSCLC患者死亡和进展的风险较高。在我们的患者中未发现IL1B rs12621220,IL1B rs1143623,IL1B rs16944,IL1B rs1143627,IL6 rs1800795,IL13 rs1881457对NSCLC临床结局没有影响。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号