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MIR548P和TRAV39是肿瘤微环境的潜在指标及食管鳞状细胞癌的新型预后生物标志物。

MIR548P and TRAV39 Are Potential Indicators of Tumor Microenvironment and Novel Prognostic Biomarkers of Esophageal Squamous Cell Carcinoma.

作者信息

Xu Jian, Tang Long, Wang Zhiqiang, Zhang Qi, Jiang Yuequan

机构信息

Chongqing Key Laboratory of Translational Research for Cancer Metastasis and Individualized Treatment, Chongqing University Cancer Hospital, Chongqing 400030, China.

出版信息

J Oncol. 2022 Sep 17;2022:3152114. doi: 10.1155/2022/3152114. eCollection 2022.

Abstract

Esophageal squamous cell carcinoma (ESCC) remains a common aggressive malignancy in the world. Multiple studies have shown evidence to support the hypothesis that certain functional genes that are engaged in the microenvironment of tumors played a role in the progression of ESCC. Thus, to better analyze the prognostic values of important genes in ESCC, there is an immediate need for an in-depth research study. From the TCGA database, the RNA-seq data and clinical features of 163 ESCC patients were obtained. Using the ESTIMATE technique, we were able to calculate the ImmuneScore, the StromalScore, and the ESTIMATEScore for each ESCC sample. The samples from the ESCC were split up into high score and low score groups based on the median of the various scores. In this study, ImmuneScore, StromalScore, and ESTIMATEScore were not found to be linked with overall survival of ESCC patients, according to our findings. Higher StromalScores were linked to more advanced T stages and clinical stages. The intersection analysis that was exhibited by the use of a Venn diagram indicated that there was a total of 944 upregulated genes that shared the same high score in both the ImmuneScore and the StromalScore and that there was 0 downregulated gene that shared the same low score. Survival experiments confirmed MIR548P and TRAV39 as critical prognostic biomarkers for ESCC patients. Importantly, we found that TRAV39 expression was positively associated with T cell CD4 memory activated while negatively associated with B cell memory, dendritic cells activated, and mast cells activated. In addition, we found that MIR548P expression was negatively associated with mast cells activated while positively associated with T cell CD4 memory activated. Overall, we identified MIR548P and TRAV39 as new modulators for ESCC, affecting the immune microenvironment of ESCC patients and may be a target of immunotherapy.

摘要

食管鳞状细胞癌(ESCC)仍是全球常见的侵袭性恶性肿瘤。多项研究已证明有证据支持以下假说:参与肿瘤微环境的某些功能基因在ESCC进展中发挥作用。因此,为了更好地分析ESCC中重要基因的预后价值,迫切需要进行深入的研究。从TCGA数据库中获取了163例ESCC患者的RNA测序数据和临床特征。使用ESTIMATE技术,我们能够计算每个ESCC样本的免疫评分、基质评分和ESTIMATE评分。根据各种评分的中位数,将ESCC样本分为高分和低分两组。根据我们的研究结果,在本研究中未发现免疫评分、基质评分和ESTIMATE评分与ESCC患者的总生存期相关。较高的基质评分与更晚期的T分期和临床分期相关。使用维恩图进行的交叉分析表明,在免疫评分和基质评分中共有944个上调基因具有相同的高分,且没有下调基因具有相同的低分。生存实验证实MIR548P和TRAV39是ESCC患者的关键预后生物标志物。重要的是,我们发现TRAV39表达与活化的CD4记忆T细胞呈正相关,而与B细胞记忆、活化的树突状细胞和活化的肥大细胞呈负相关。此外,我们发现MIR548P表达与活化的肥大细胞呈负相关,而与活化的CD4记忆T细胞呈正相关。总体而言,我们确定MIR548P和TRAV39是ESCC的新调节因子,影响ESCC患者的免疫微环境,可能是免疫治疗的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0c9/9509226/a86f6e030627/JO2022-3152114.001.jpg

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