Suppr超能文献

HMGCS2对中国食管鳞状细胞癌切除患者预后的预测意义

Predictive significance of HMGCS2 for prognosis in resected Chinese esophageal squamous cell carcinoma patients.

作者信息

Tang Hong, Wu Yufeng, Qin Yanru, Wang Hongyan, Jia Yongxu, Yang Shujun, Luo Suxia, Wang Qiming

机构信息

Department of Internal Medicine, Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer Hospital.

Department of Clinical Oncology, the First Affiliated Hospital, Zhengzhou University, Zhengzhou, Henan, China.

出版信息

Onco Targets Ther. 2017 May 15;10:2553-2560. doi: 10.2147/OTT.S132543. eCollection 2017.

Abstract

Despite a series of attempts during the last decades, the prognosis of esophageal squamous cell carcinoma (ESCC) remains poor. Different responses of individual tumors encouraged us to look for valuable prognostic markers. As a key regulator controlling the anabolic ketogenic pathway, 3-hydroxy-3-methylglutaryl-CoA synthase 2 () has been reported to play a crucial role in colorectal cancer and prostate cancer. However, its importance to ESCC has not been verified. Therefore, a large cohort retrospective study was planned, to investigate the relationship between expression and ESCC prognosis. By adopting real-time polymerase chain reaction (PCR) and immunohistochemical (IHC) staining, expression was examined in tissues of 300 ESCC patients with complete resection. Besides, the association between HMGCS2 protein expression and survival time was evaluated through chi-square test and Kaplan-Meier analysis. With the use of Cox-proportional hazards model, the prognostic impact of clinicopathologic variables and biomarker expression was evaluated. Compared with their non-tumor counterparts, downregulation occurred in 65.5% and 37.6% of primary ESCCs on the mRNA and protein levels (<0.001), respectively. On the protein level, HMGCS2 expression was associated with tumor cell differentiation (=0.003), pT status (=0.006), and TNM stage (=0.010). In the down-HMGCS2 expression group, the 5-year overall survival (OS) and relapse-free survival (RFS) are poorer than those in the normal expression group (19 months vs 24 months, =0.002; 13 months vs 17 months, =0.007, respectively). According to the TNM stage, stratified analysis revealed that its discernibility on RFS was only pronounced in patients with advanced clinical stage (=0.001). In addition, multivariate Cox regression analysis showed that HMGCS2 expression was an independent risk factor for RFS (=0.032) instead of OS (=0.099). The findings of this study provided the evidence that HMGSC2 represented a potential novel prognostic biomarker for ESCC patients.

摘要

尽管在过去几十年间进行了一系列尝试,但食管鳞状细胞癌(ESCC)的预后仍然很差。个体肿瘤的不同反应促使我们寻找有价值的预后标志物。作为控制合成代谢生酮途径的关键调节因子,3-羟基-3-甲基戊二酰辅酶A合酶2(HMGCS2)已被报道在结直肠癌和前列腺癌中起关键作用。然而,其对ESCC的重要性尚未得到证实。因此,我们计划开展一项大型队列回顾性研究,以调查HMGCS2表达与ESCC预后之间的关系。通过采用实时聚合酶链反应(PCR)和免疫组织化学(IHC)染色,检测了300例接受根治性切除的ESCC患者组织中的HMGCS2表达。此外,通过卡方检验和Kaplan-Meier分析评估了HMGCS2蛋白表达与生存时间之间的关联。使用Cox比例风险模型,评估了临床病理变量和生物标志物表达的预后影响。与非肿瘤组织相比,原发性ESCC中HMGCS2在mRNA和蛋白水平的下调发生率分别为65.5%和37.6%(P<0.001)。在蛋白水平上,HMGCS2表达与肿瘤细胞分化(P=0.003)、pT状态(P=0.006)和TNM分期(P=0.010)相关。在HMGCS2低表达组中,5年总生存(OS)和无复发生存(RFS)均低于正常表达组(分别为19个月对24个月,P=0.002;13个月对17个月,P=0.007)。根据TNM分期进行的分层分析显示,其对RFS的辨别能力仅在临床晚期患者中显著(P=0.001)。此外,多因素Cox回归分析显示,HMGCS2表达是RFS的独立危险因素(P=0.032),而非OS的独立危险因素(P=0.099)。本研究结果提供了证据,表明HMGSC2是ESCC患者潜在的新型预后生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e24/5438074/22059884737a/ott-10-2553Fig1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验