Characterization of platelet-related genes and constructing signature combined with immune-related genes for predicting outcomes and immunotherapy response in lung squamous cell carcinoma

被引:0
|
作者
Zhao, Siyi [1 ,2 ,3 ,4 ,5 ]
Gong, Han [1 ,2 ,3 ,4 ,6 ,7 ]
Liang, Wenhua [1 ,2 ,3 ,4 ]
机构
[1] Guangzhou Med Univ, Affiliated Hosp 1, Dept Thorac Surg & Oncol, Guangzhou, Peoples R China
[2] Guangzhou Inst Resp Dis, Guangzhou, Peoples R China
[3] China State Key Lab Resp Dis, Guangzhou, Peoples R China
[4] Natl Clin Res Ctr Resp Dis, Guangzhou, Peoples R China
[5] Guangzhou Med Univ, Dept Clin Med, Clin Med Sch 1, Guangzhou, Peoples R China
[6] Cent South Univ, Mol Biol Res Ctr, Sch Life Sci, Changsha, Hunan, Peoples R China
[7] Cent South Univ, Ctr Med Genet, Sch Life Sci, Changsha, Hunan, Peoples R China
来源
AGING-US | 2023年 / 15卷 / 14期
基金
中国国家自然科学基金;
关键词
lung squamous cell carcinoma; platelet-related genes; prognosis; immunity; tumor microenvironments; CANCER; PROGNOSIS; LANDSCAPE; MARKERS; COUNT;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Lung squamous cell carcinoma (LUSC) is a highly malignant subtype of non-small cell lung cancer with poor prognosis. Platelets are known to play a critical role in cancer development and progression, and recent studies suggest that they can also regulate immune response in tumors. However, the relationship between plateletrelated genes (PRGs) and LUSC prognosis and tumor microenvironments remains unclear. In this study, we used multiple bioinformatics algorithms to identify 25 dysregulated PRGs that were significantly associated with LUSC prognosis. We found that PRGs were involved in multiple biological processes, particularly in the tumor microenvironment, and that platelet-related scores (PRS) were a risk factor. Additionally, we established a 6-gene prognostic signature combining PRGs and immune-related genes that accurately predicted outcomes and immunotherapy efficacy in LUSC patients. Our study provides a comprehensive analysis of the biological functions and potential therapeutic targets of PRGs in LUSC, which may inform the development of new treatments for this disease.
引用
收藏
页码:6969 / 6992
页数:24
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