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FDC-SP 作为诊断和预后生物标志物,并调节肾细胞癌中的免疫浸润。

FDC-SP as a diagnostic and prognostic biomarker and modulates immune infiltrates in renal cell carcinoma.

机构信息

Department of Urology, The Third Central Clinical College of Tianjin Medical University, Tianjin, 300170, China.

Department of Urology, The Third Central Hospital of Tianjin, 83 Jintang Road, Hedong District, Tianjin, 300170, China.

出版信息

BMC Bioinformatics. 2023 Mar 10;24(1):91. doi: 10.1186/s12859-023-05215-1.

DOI:10.1186/s12859-023-05215-1
PMID:36899339
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10007807/
Abstract

BACKGROUND

Renal cell carcinoma (RCC), one of the top 10 causes of cancer death, is responsible for more than 90% of all cases of primary renal cancer worldwide. Follicular dendritic cell-secreted protein (FDC-SP) specifically binds to activated B cells and regulates the generation of antibodies. It is also thought to promote cancer cell invasion and migration, which could help with tumor metastases. This study aimed to assess the efficacy of FDC-SP in the diagnosis and prognosis of RCC and to investigate the relationship between immune infiltration in RCC and these outcomes.

RESULTS

RCC tissues had significantly higher levels of FDC-SP protein and mRNA than normal tissues. The high level of FDC-SP expression was linked to the T stage, histological grade, pathological stage, N stage, M stage, and OS event. Functional enrichment analysis identified the major pathways that were enriched as immune response regulation, complement, and coagulation. Immunological checkpoints and immune cell infiltration were observed to substantially correlate with the levels of FDC-SP expression. FDC-SP expression levels showed the ability to precisely distinguish high-grade or high-stage renal cancer (area under the curve (AUC) = 0.830, 0.722), and RCC patients with higher FDC-SP expression levels had worse prognoses. The AUC values for one-, two-, and five-year survival rates were all greater than 0.600. Moreover, the FDC-SP expression is an independent predictive biomarker of OS in RCC patients.

CONCLUSION

FDC-SP may be a prospective therapeutic target in RCC as well as a possible diagnostic and prognostic biomarker associated with immune infiltration.

摘要

背景

肾细胞癌(RCC)是癌症死亡的十大原因之一,占全球所有原发性肾癌的 90%以上。滤泡树突状细胞分泌蛋白(FDC-SP)特异性结合激活的 B 细胞,并调节抗体的产生。它还被认为可促进癌细胞的侵袭和迁移,这有助于肿瘤转移。本研究旨在评估 FDC-SP 在 RCC 诊断和预后中的作用,并探讨 RCC 中的免疫浸润与这些结果的关系。

结果

RCC 组织中的 FDC-SP 蛋白和 mRNA 水平明显高于正常组织。高水平的 FDC-SP 表达与 T 分期、组织学分级、病理分期、N 分期、M 分期和 OS 事件有关。功能富集分析确定了主要的富集途径为免疫反应调节、补体和凝血。免疫检查点和免疫细胞浸润与 FDC-SP 表达水平显著相关。FDC-SP 表达水平能够准确地区分高级或高分期的肾癌(曲线下面积(AUC)=0.830,0.722),且 FDC-SP 高表达的 RCC 患者预后较差。AUC 值在 1 年、2 年和 5 年生存率的均大于 0.600。此外,FDC-SP 表达是 RCC 患者 OS 的独立预测生物标志物。

结论

FDC-SP 可能是 RCC 的一种有前途的治疗靶点,也是一种与免疫浸润相关的可能的诊断和预后生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4379/10007807/dbfb06eed010/12859_2023_5215_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4379/10007807/a3b0752af4f1/12859_2023_5215_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4379/10007807/769f381df9b2/12859_2023_5215_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4379/10007807/c228940f80f6/12859_2023_5215_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4379/10007807/036421a97fe5/12859_2023_5215_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4379/10007807/7d3852267f55/12859_2023_5215_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4379/10007807/75fd60d4050a/12859_2023_5215_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4379/10007807/dbfb06eed010/12859_2023_5215_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4379/10007807/a3b0752af4f1/12859_2023_5215_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4379/10007807/769f381df9b2/12859_2023_5215_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4379/10007807/c228940f80f6/12859_2023_5215_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4379/10007807/036421a97fe5/12859_2023_5215_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4379/10007807/7d3852267f55/12859_2023_5215_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4379/10007807/75fd60d4050a/12859_2023_5215_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4379/10007807/dbfb06eed010/12859_2023_5215_Fig7_HTML.jpg

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