Revolutionizing prognosis: Introducing cell death index (CDI) as a powerful prognostic tool for CSCC patients

IF 3.2 3区 医学 Q2 ENVIRONMENTAL SCIENCES
Rongjun Tang, Qing Yao, Ke Zhang, Qingqing Yu, Jun Lou, Lingdi Li
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引用次数: 0

Abstract

Background

Cervical squamous cell carcinoma (CSCC) threatens the body health of women worldwide. This study aimed to foster a new concept of prognostic indicator named cell death index (CDI).

Methods

RNA-seq and scRNA-seq datasets were downloaded from the GEO and TCGA database as the training and validation cohorts. Programmed cell death (PCD)-related gene signatures were obtained from published research. The construction of prognostic model was performed based on CDI value. Patients with CSCC were divided into high- and low-CDI groups. We explored the differences in overall survival time, immune infiltration, mutation status, and drug sensitivity between high and low CDI groups by R software.

Results

We constructed prognostic model to calculate the CDI value with 23 genes. Patients with high CDI have shorter survival time than those with low CDI. CDI was considered a risk factor compared to other characteristics. The nomogram model estimated overall survival (OS) at 1, 3, and 6 years, with age, Stage, and CDI, indicating the accuracy of the model in predicting 1-, 3-, and 6-year survival rates. CDI values were negatively correlated with most immune checkpoint genes. We measured the significant drug sensitivity of Mitoxantrone, Sabutoclax, Sepantronium bromide, Topotecan, BI-2536, and BMS-754807 between high- and low-CDI groups with significant correlation.

Conclusion

This investigation constructed a novel effective prognostic indicator of CDI in patients with CSCC and identified potential genes associated with cell death that could be targeted for prognosis and treatment of CSCC.

革命性的预后:引入细胞死亡指数(CDI)作为CSCC患者的强大预后工具。
背景:宫颈鳞状细胞癌(CSCC)威胁着全世界妇女的身体健康。本研究旨在提出一种新的预后指标概念——细胞死亡指数(CDI)。方法:从GEO和TCGA数据库下载RNA-seq和scRNA-seq数据集作为训练和验证队列。程序性细胞死亡(PCD)相关的基因特征从已发表的研究中获得。基于CDI值构建预后模型。将CSCC患者分为高cdi组和低cdi组。采用R软件分析CDI高、低组患者的总生存时间、免疫浸润、突变状态、药物敏感性等差异。结果:构建预后模型,计算23个基因的CDI值。高CDI患者的生存时间比低CDI患者短。与其他特征相比,CDI被认为是一个危险因素。nomogram模型估计了1年、3年和6年的总生存率(OS),包括年龄、分期和CDI,表明该模型预测1年、3年和6年生存率的准确性。CDI值与大多数免疫检查点基因呈负相关。我们测量了米托蒽醌、沙布托克、溴化塞泮曲铵、拓扑替康、BI-2536和BMS-754807在高、低cdi组之间的显著药物敏感性,且具有显著相关性。结论:本研究构建了CSCC患者CDI的一种新的有效预后指标,并发现了与细胞死亡相关的潜在基因,可用于CSCC的预后和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Environmental Toxicology
Environmental Toxicology 环境科学-毒理学
CiteScore
7.10
自引率
8.90%
发文量
261
审稿时长
4.5 months
期刊介绍: The journal publishes in the areas of toxicity and toxicology of environmental pollutants in air, dust, sediment, soil and water, and natural toxins in the environment.Of particular interest are: Toxic or biologically disruptive impacts of anthropogenic chemicals such as pharmaceuticals, industrial organics, agricultural chemicals, and by-products such as chlorinated compounds from water disinfection and waste incineration; Natural toxins and their impacts; Biotransformation and metabolism of toxigenic compounds, food chains for toxin accumulation or biodegradation; Assays of toxicity, endocrine disruption, mutagenicity, carcinogenicity, ecosystem impact and health hazard; Environmental and public health risk assessment, environmental guidelines, environmental policy for toxicants.
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