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ETV1 与结直肠癌中的免疫浸润和不良临床预后呈正相关。

ETV1 Positively Correlated With Immune Infiltration and Poor Clinical Prognosis in Colorectal Cancer.

机构信息

Department of Gastroenterology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Shanghai Institute of Digestive Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

Front Immunol. 2022 Jul 4;13:939806. doi: 10.3389/fimmu.2022.939806. eCollection 2022.

Abstract

OBJECTIVE

Numerous studies recently suggested that the immune microenvironment could influence the development of colorectal cancer (CRC). These findings implied that the infiltration of immune cells could be a promising prognostic biomarker for CRC.

METHODS

Furthermore, the Oncomine database and R2 platform analysis were applied in our research to validate CRC clinical prognosis expression levels of polyoma enhancer activator 3 (PEA3) members. We explored the correlation of ETV1, ETV4, and ETV5 with tumor-infiltrating immune cells (TIICs) in CRC tumor microenvironments the Tumor Immune Estimation Resource (TIMER) and Gene Expression Profiling Interactive Analysis (GEPIA). Immunohistochemistry (IHC) was used to validate our CRC clinical data.

RESULTS

Our findings indicated that the upregulation of PEA3 members including ETV1 and ETV5 was positively associated with poor prognosis in CRC patients. Meanwhile, ETV1 and ETV5 may play significant roles in the development progress of CRC. Furthermore, ETV1 tends to be associated with immune infiltration of CRC, especially with cancer-associated fibroblasts and M2 macrophages.

CONCLUSION

These findings revealed that ETV1 and ETV5 played significant roles in the development of CRC. Moreover, ETV1 was significantly associated with the infiltration of cancer-associated fibroblasts and M2 macrophages in CRC. Targeting ETV1 can be a potential auspicious approach for CRC treatment.

摘要

目的

最近有大量研究表明,免疫微环境可能会影响结直肠癌(CRC)的发展。这些发现表明,免疫细胞的浸润可能是 CRC 的一种有前途的预后生物标志物。

方法

此外,我们的研究还应用了 Oncomine 数据库和 R2 平台分析来验证 CRC 临床预后中多瘤增强子激活物 3(PEA3)成员的表达水平。我们探讨了 ETV1、ETV4 和 ETV5 与 CRC 肿瘤微环境中肿瘤浸润免疫细胞(TIICs)的相关性——使用 Tumor Immune Estimation Resource(TIMER)和 Gene Expression Profiling Interactive Analysis(GEPIA)。免疫组织化学(IHC)用于验证我们的 CRC 临床数据。

结果

我们的研究结果表明,PEA3 成员(包括 ETV1 和 ETV5)的上调与 CRC 患者的不良预后呈正相关。同时,ETV1 和 ETV5 可能在 CRC 的发展进程中发挥重要作用。此外,ETV1 往往与 CRC 的免疫浸润有关,特别是与癌症相关成纤维细胞和 M2 巨噬细胞有关。

结论

这些发现表明 ETV1 和 ETV5 在 CRC 的发展中发挥了重要作用。此外,ETV1 与 CRC 中癌症相关成纤维细胞和 M2 巨噬细胞的浸润显著相关。靶向 ETV1 可能是 CRC 治疗的一种有前途的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a77a/9291282/ed22af91a0ec/fimmu-13-939806-g001.jpg

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