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2
Preliminary study using a small plasma extracellular vesicle miRNA panel as a potential biomarker for early diagnosis and prognosis in laryngeal cancer.初步研究使用小型血浆细胞外囊泡 miRNA 面板作为喉癌早期诊断和预后的潜在生物标志物。
Cell Oncol (Dordr). 2023 Aug;46(4):1015-1030. doi: 10.1007/s13402-023-00792-y. Epub 2023 Mar 25.
3
Promotes Laryngeal Carcinoma Proliferation and Migration Through Pathway by .通过……途径促进喉癌增殖和迁移。 (原文表述不完整,翻译可能不太准确,完整准确的翻译需补充完整原文信息)
Iran J Biotechnol. 2023 Jan 1;21(1):e3339. doi: 10.30498/ijb.2022.336501.3339. eCollection 2023 Jan.
4
Reirradiation for local recurrence of oral, pharyngeal, and laryngeal cancers: a multi-institutional study.口腔、咽和喉癌局部复发的再放疗:一项多机构研究。
Sci Rep. 2023 Feb 21;13(1):3062. doi: 10.1038/s41598-023-29459-2.
5
Identification of immunocell infiltrates and effective diagnostic biomarkers in laryngeal carcinoma.鉴定喉癌中的免疫细胞浸润和有效诊断生物标志物。
Medicine (Baltimore). 2023 Jan 20;102(3):e32548. doi: 10.1097/MD.0000000000032548.
6
Pan-cancer genetic analysis of cuproptosis and copper metabolism-related gene set.铜死亡及铜代谢相关基因集的泛癌基因分析
Front Oncol. 2022 Oct 6;12:952290. doi: 10.3389/fonc.2022.952290. eCollection 2022.
7
KIF26B-AS1 Regulates TLR4 and Activates the TLR4 Signaling Pathway to Promote Malignant Progression of Laryngeal Cancer.KIF26B-AS1 通过调控 TLR4 并激活 TLR4 信号通路促进喉癌的恶性进展。
J Microbiol Biotechnol. 2022 Oct 28;32(10):1344-1354. doi: 10.4014/jmb.2203.03037. Epub 2022 Jul 8.
8
Increased expression of ST2 on regulatory T cells is associated with cancer associated fibroblast-derived IL-33 in laryngeal cancer.调节性 T 细胞上 ST2 的表达增加与喉癌中癌相关成纤维细胞衍生的 IL-33 有关。
Pathol Res Pract. 2022 Sep;237:154023. doi: 10.1016/j.prp.2022.154023. Epub 2022 Jul 13.
9
Epidemiological, clinical and oncological outcomes of young patients with laryngeal cancer: a systematic review.年轻喉癌患者的流行病学、临床和肿瘤学结局:系统评价。
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10
Gold Nanostars Combined with the Searched Antibody for Targeted Oral Squamous Cell Carcinoma Therapy.金纳米星与靶向搜索抗体联合用于口腔鳞状细胞癌的靶向治疗。
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喉癌铜死亡亚型相关基因的分子特征、免疫相关性分析、WGCNA 分析和机器学习建模。

Molecular characterization, immunocorrelation analysis, WGCNA analysis and machine learning modeling of genes associated with copper death subtypes of laryngeal cancer.

机构信息

Department of Otolaryngology, Wenzhou Hospital of Integrated Traditional Chinese and Western Medicine, Wenzhou, China.

Department of Otolaryngology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.

出版信息

Technol Health Care. 2024;32(6):4707-4725. doi: 10.3233/THC-240932.

DOI:10.3233/THC-240932
PMID:39302398
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11613018/
Abstract

BACKGROUND

Laryngeal cancer is a malignant tumor that originates from the mucous membrane of the larynx. Currently, the specific involvement mechanism of copper death in laryngeal cancer patients has not been deeply studied.

OBJECTIVE

This study aims to explore the molecular characteristics and clinical survival significance of copper death-related genes in laryngeal cancer.

METHODS

Relevant transcriptomes and clinical data were retrieved and downloaded from the GEO database. Differential expression genes related to laryngeal cancer and copper death were selected, and the immune function, clinical risk correlation, and survival prognosis were analyzed.

RESULTS

The differential analysis results showed that the differential expression genes related to laryngeal cancer and Cu-proptosis included SLC31A1 and ATP7B, and there was interaction between the immune cell groups in the differential genes of copper death in laryngeal cancer. Decreasing the expression of the gene ANXA5 or increasing the expression of the gene SERPINH1 can increase the susceptibility to laryngeal cancer.

CONCLUSION

Copper death-related genes can affect the survival prognosis of laryngeal cancer patients. Detection of changes in their expression can provide new diagnostic and treatment directions for the progression of early-stage laryngeal cancer.

摘要

背景

喉癌是一种起源于喉部黏膜的恶性肿瘤。目前,铜死亡在喉癌患者中具体的参与机制尚未深入研究。

目的

本研究旨在探讨铜死亡相关基因在喉癌中的分子特征和临床生存意义。

方法

从 GEO 数据库中检索并下载与喉癌和铜死亡相关的转录组和临床数据,筛选出与喉癌和铜死亡相关的差异表达基因,并分析其免疫功能、临床风险相关性和生存预后。

结果

差异分析结果显示,与喉癌和铜死亡相关的差异表达基因包括 SLC31A1 和 ATP7B,并且在喉癌铜死亡的差异基因中存在免疫细胞群之间的相互作用。降低基因 ANXA5 的表达或增加基因 SERPINH1 的表达均可增加患喉癌的易感性。

结论

铜死亡相关基因可影响喉癌患者的生存预后。检测其表达变化可为早期喉癌的进展提供新的诊断和治疗方向。