Guan Lingling, Zeng Runhao, Chen Yi, He Guohua, Yao Wenxia, Liu Zhaoyu, Liu Hui
Precision Medicine Center, The Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, 510000, China.
The State Key Laboratory of Respiratory Disease and National Clinical Research Center for Respiratory Disease, Guangzhou, China.
Sci Rep. 2024 Dec 28;14(1):31518. doi: 10.1038/s41598-024-82973-9.
Polyomavirus enhancer activator 3 (PEA3), an ETS transcription factor, has been documented to regulate the development and metastasis of human cancers. Nonetheless, a thorough analysis examining the relationship between the PEA3 subfamily members and tumour development, prognosis, and the tumour microenvironment (TME) across various cancer types has not yet been conducted. The expression profiles and prognostic significance of the PEA3 subfamily were evaluated using data from the GEO, TCGA, and PrognoScan databases, in conjunction with COX regression analyses and the Kaplan-Meier Plotter. Furthermore, the relationships between PEA3 subfamily expression, stemness scores, tumor microenvironments, immune subtypes, and drug susceptibility across multiple cancer types were explored. We found that ETV1, ETV4 and ETV5 are highly expressed in cancer, and their biological functions are synergistic. In the prognostic analysis of the Cancer Genome Atlas, the PEA3 subfamily genes were found to be associated with the prognosis of multiple cancers such as Lung adenocarcinoma (LUAD), Liver hepatocellular carcinoma (LIHC), etc., and marked a worse prognosis at different endpoints. In addition, it was significantly correlated with the stromal and immune scores of pan-cancer, and also significantly associated with the RNA stemness score and DNA stemness score of pan-cancer. Expression levels of the PEA3 subfamily genes correlate with immune subtypes of LIHC, LUAD, and Lung squamous cell carcinoma. We also found a variety of drugs with positive and negative associations of ETV1, ETV4 and ETV5. These findings elucidate the role of the PEA3 subfamily gene as a biomarker for carcinogenesis and cancer progression, offering valuable insights for future research into the PEA3 subfamily gene as a potential therapeutic target across various cancer types.
多瘤病毒增强子激活因子3(PEA3)是一种ETS转录因子,已被证明可调节人类癌症的发展和转移。然而,尚未对PEA3亚家族成员与各种癌症类型的肿瘤发展、预后和肿瘤微环境(TME)之间的关系进行全面分析。使用来自GEO、TCGA和PrognoScan数据库的数据,结合COX回归分析和Kaplan-Meier Plotter,评估了PEA3亚家族的表达谱和预后意义。此外,还探讨了多种癌症类型中PEA3亚家族表达、干性评分、肿瘤微环境、免疫亚型和药物敏感性之间的关系。我们发现ETV1、ETV4和ETV5在癌症中高表达,它们的生物学功能具有协同作用。在癌症基因组图谱的预后分析中,发现PEA3亚家族基因与多种癌症如肺腺癌(LUAD)、肝细胞癌(LIHC)等的预后相关,并且在不同终点显示出较差的预后。此外,它与泛癌的基质和免疫评分显著相关,也与泛癌的RNA干性评分和DNA干性评分显著相关。PEA3亚家族基因的表达水平与LIHC、LUAD和肺鳞状细胞癌的免疫亚型相关。我们还发现了多种与ETV1、ETV4和ETV5有正负关联的药物。这些发现阐明了PEA3亚家族基因作为致癌和癌症进展生物标志物的作用,为未来将PEA3亚家族基因作为各种癌症类型潜在治疗靶点的研究提供了有价值的见解。