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PRF1 作为皮肤黑色素瘤淋巴转移的预后基因。

PRF1 as a prognostic gene for lymphatic metastasis in skin melanoma.

机构信息

Department of Oncology, Zhongshan Hospital (Xiamen), Fudan University, Xiamen, China; Clinical Research Center for Precision Medicine of Abdominal Tumor of Fujian Province, China.

Department of General Practice, Zhongshan Hospital (Xiamen), Fudan University, China.

出版信息

Biochem Biophys Res Commun. 2024 Nov 19;734:150338. doi: 10.1016/j.bbrc.2024.150338. Epub 2024 Jul 23.

Abstract

BACKGROUND

Melanoma is a highly aggressive tumor, predominantly found in the skin, recognized as skin cutaneous melanoma (SKCM). Lymph node metastasis is commonly used as the route of metastasis in SKCM, necessitating the discovery of prognostic genes associated with this process for improved prognosis.

METHODS

The prognostic significance of lymph node metastasis in SKCM was assessed through Kaplan-Meier analysis in SEER and TCGA-SKCM datasets. Prognostic genes were identified and a prognostic risk model was constructed Enrichment analysis and immune cell infiltration analysis were also carried out.Moreover, a validation in vitro and in vivo were conducted by CCK8,flow cytometry, transwell and animal study.

RESULTS

The Kaplan-Meier survival curve revealed that patients with lymph node metastasis had a worse prognosis compared to those without. FCGR3B and PRF1 were screened by TCGA analysis.Additionally, significant differences in nine immune cell types were observed between the two risk groups. Notably, a strong positive association with CD8 T cells and a negative relationship with M2 macrophages were exhibited by PRF1. The validation of our nomogram were conducted in vitro and in vivo, and the results showed the correlations between CD8 T cell and PRF1.

CONCLUSION

In summary, two prognostic genes (FCGR3B and PRF1) were identified, and a prognostic risk model was developed for SKCM. These findings provide a novel approach for the diagnosis and treatment of SKCM.

摘要

背景

黑色素瘤是一种高度侵袭性的肿瘤,主要发生在皮肤,被称为皮肤黑色素瘤(SKCM)。淋巴结转移通常是 SKCM 转移的途径,因此需要发现与该过程相关的预后基因,以改善预后。

方法

通过 SEER 和 TCGA-SKCM 数据集的 Kaplan-Meier 分析评估 SKCM 中淋巴结转移的预后意义。识别预后基因,并构建预后风险模型。进行富集分析和免疫细胞浸润分析。此外,通过 CCK8、流式细胞术、transwell 和动物研究进行了体外和体内验证。

结果

Kaplan-Meier 生存曲线显示,有淋巴结转移的患者预后比没有淋巴结转移的患者差。通过 TCGA 分析筛选出 FCGR3B 和 PRF1。此外,两个风险组之间观察到 9 种免疫细胞类型存在显著差异。值得注意的是,PRF1 与 CD8 T 细胞呈强正相关,与 M2 巨噬细胞呈负相关。我们的列线图在体外和体内进行了验证,结果显示 CD8 T 细胞和 PRF1 之间存在相关性。

结论

总之,鉴定了两个预后基因(FCGR3B 和 PRF1),并为 SKCM 开发了一个预后风险模型。这些发现为 SKCM 的诊断和治疗提供了新的方法。

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