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APE1 可能影响早期 NSCLC 中无复发生存期的 CD4+ 幼稚 T 细胞。

APE1 may influence CD4+ naïve T cells on recurrence free survival in early stage NSCLC.

机构信息

School of Nursing, Chongqing Medical and Pharmaceutical College, No. 82, Daxuecheng Rd, Shapingba Dist, Chongqing, 401331, China.

Cancer Center, Daping Hospital, Army Medical University (Third Military Medical University), No. 10 Changjiang Zhi Rd., Yuzhong Dist, Chongqing, 400042, China.

出版信息

BMC Cancer. 2021 Mar 6;21(1):233. doi: 10.1186/s12885-021-07950-1.

Abstract

BACKGROUND

It was demonstrated that multifunctional protein APE1 (Apurinic/apyrimidinic endonuclease 1) is closely related to tumor immune microenvironment in a number of investigations, Meanwhile, the abundance of tumor infiltrating lymphocytes (TILs) has been shown as a prognosis indicator in some researches. However, it remains unclear whether APE1 is involved in the process of TILs affecting the prognosis of patients. To this end, we investigated the associations between APE1 and TILs in non-small cell lung cancer (NSCLC) and explored whether APE1 would influence the associations of CD4 T cells infiltration with the prognosis of patients.

METHODS

Genome-wide expression datasets were obtained from the Gene Expression Omnibus (GEO) public database under accession number GSE68465, GSE30219, GSE31210 and GSE50081. MCPcounter and CIBERSORT analysis was conducted to evaluate the abundance of TILs in 1006 NSCLC patients of GEO database. Spearman correlation tests were used to evaluate correlations between abundance of various TILs and APE1 expression. RFS (recurrence free survival) was estimated using the Kaplan-Meier method and the Cox proportional-hazards model. The expression level of APE1 and tumor-infiltrating CD4 T cells was evaluated by immunohistochemistry (IHC).

RESULTS

The results showed that the abundance of CD4 naïve T cells was negatively associated with the APE1 expression. CD4 naïve T cells infiltration was a favorable prognostic factor for RFS, however, there was no effect of CD4 T cells infiltration on RFS in patients with high APE1 expression. Subsequently, it was further confirmed that CD4 T cells infiltration was negatively associated with the APE1 expression level in 108 NSCLC tissue samples; high CD4 T cells infiltration was associated with longer RFS in low APE1 expression group but not in APE1 high expression group.

CONCLUSION

These results suggested that APE1 may affect the relationship between CD4 T cells infiltration and prognosis in NSCLC. This study provides new insights into predictors of outcome in patients with NSCLC, and suggests that combining immunotherapy and APE1-targeted therapy may be a promising treatment for NSCLC.

摘要

背景

多项研究表明,多功能蛋白 APE1(脱嘌呤/脱嘧啶核酸内切酶 1)与肿瘤免疫微环境密切相关。同时,肿瘤浸润淋巴细胞(TILs)的丰度在一些研究中被证明是预后指标。然而,APE1 是否参与 TILs 影响患者预后的过程尚不清楚。为此,我们研究了非小细胞肺癌(NSCLC)中 APE1 与 TILs 的相关性,并探讨了 APE1 是否会影响 CD4 T 细胞浸润与患者预后的相关性。

方法

从基因表达综合数据库(GEO)公共数据库中获取基因表达数据集,以 GSE68465、GSE30219、GSE31210 和 GSE50081 作为访问号。使用 MCPcounter 和 CIBERSORT 分析方法评估 1006 例 NSCLC 患者 GEO 数据库中 TILs 的丰度。采用 Spearman 相关检验评估各种 TILs 与 APE1 表达之间的相关性。采用 Kaplan-Meier 法和 Cox 比例风险模型估计无复发生存率(RFS)。采用免疫组织化学(IHC)评估 APE1 和肿瘤浸润性 CD4 T 细胞的表达水平。

结果

结果表明,CD4 幼稚 T 细胞的丰度与 APE1 的表达呈负相关。CD4 幼稚 T 细胞浸润是 RFS 的有利预后因素,但在 APE1 高表达患者中,CD4 T 细胞浸润对 RFS 无影响。随后,在 108 例 NSCLC 组织样本中进一步证实,CD4 T 细胞浸润与 APE1 表达水平呈负相关;在 APE1 低表达组中,高 CD4 T 细胞浸润与 RFS 延长相关,但在 APE1 高表达组中则无此相关性。

结论

这些结果表明,APE1 可能影响 NSCLC 中 CD4 T 细胞浸润与预后的关系。本研究为 NSCLC 患者的预后预测提供了新的见解,并表明联合免疫治疗和 APE1 靶向治疗可能是 NSCLC 的一种有前途的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed4b/7937314/af27b6079c4a/12885_2021_7950_Fig1_HTML.jpg

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