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一种用于乳腺肿瘤浸润免疫细胞和药物敏感性的免疫相关长链非编码 RNA 对的新型预后特征

英文原题:A Novel Prognostic Signature of Immune-Related Long Noncoding RNA Pairs for Tumor-Infiltrating Immune Cells and Drug Susceptibility in Breast Cancer.

查看英文原题

A Novel Prognostic Signature of Immune-Related Long Noncoding RNA Pairs for Tumor-Infiltrating Immune Cells and Drug Susceptibility in Breast Cancer.

PubMed 2021/11/11(内容时间) DNA Cell Biol Q2 · IF 2.6(JCR 2025)

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中文摘要

随着乳腺癌免疫治疗的发展,特定免疫相关长链非编码RNA(irlncRNA)的预后特征已被阐明,但不同患者间基因表达的异质性仍限制了其有效性。

我们基于差异表达irlncRNA(DEirlncRNA)配对的相对表达构建了一个新的预后特征,并分析了其在来自癌症基因组图谱-乳腺癌(TCGA-BRCA)的1069例患者中的临床应用,其中包括745例白人患者、180例黑人和非裔美国人患者、58例亚洲患者、181例I期患者、606例II期患者、240例III期患者和20例IV期患者。TCGA-BRCA和ImmPort的数据用于筛选DEirlncRNA,并通过每个DEirlncRNA的循环单次比较建立DEirlncRNA配对。数据优化后,我们构建了一个包含24个DEirlncRNA配对的预后特征。该特征的风险分组使用10年生存受试者工作特征曲线的截断值进行定义,Kaplan-Meier分析验证了其预后有效性。

此外,我们证实该特征是一个独立预后因素,并确认其与传统临床病理因素密切相关。而且,该风险特征与肿瘤浸润免疫细胞和药物敏感性密切相关。简而言之,我们成功构建了一个DEirlncRNA配对的风险特征,这可能为乳腺癌精准治疗提供新的见解。

展开英文摘要原文

Prognostic signatures of specific immune-related long noncoding RNAs (irlncRNAs) have been elucidated with the development of immunotherapy for breast cancer, but the heterogeneity of gene expression in different patients still limits their effectiveness.

We constructed a new prognostic signature based on the relative expression of differentially expressed irlncRNA (DEirlncRNA) pairs and analyzed its clinical application in 1069 patients from The Cancer Genome Atlas-Breast Cancer (TCGA-BRCA) containing 745 White patients, 180 Black and African American patients, 58 Asian patients, 181 stage I patients, 606 stage II patients, 240 stage III patients, and 20 stage IV patients.

Data from TCGA-BRCA and ImmPort were used to screen DEirlncRNAs, and the DEirlncRNA pairs were established by cyclical single comparison of each DEirlncRNA. After the data optimization, we constructed a signature containing 24 DEirlncRNA pairs. Risk groups of this signature were defined using the cutoff value from the 10-year survival receiver operating characteristic curve, and Kaplan-Meier analysis verified its prognostic effectiveness.

Furthermore, we confirmed this signature as an independent prognostic factor and confirmed its close association with traditional clinicopathological factors.

Moreover, this risk signature was closely related to tumor-infiltrating immune cells and drug susceptibility. In short, we successfully constructed a risk signature of DEirlncRNA pairs, which might provide new insights for breast cancer precision therapy.

论文信息

作者
Li S、Sun X、Li J、Zheng A、Cao Y、Guo Y、Jin F
单位
Department of Breast Surgery, The First Affiliated Hospital of China Medical University, Shenyang, China.China
期刊
DNA and cell biology2022 Feb
原文标识
PubMed 34762509 · DOI 10.1089/dna.2021.0489