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CLEC11A作为结肠腺癌预后和免疫治疗反应的潜在生物标志物。

CLEC11A as a potential biomarker for prognosis and response to immunotherapy in colon adenocarcinoma.

作者信息

Gu Yuyang, Li Yanjun, Qian Tingting, Xu Xiaofang

机构信息

Department of Oncology, The First Hospital of Jiaxing, Affiliated Hospital of Jiaxing University, Jiaxing, 314000, Zhejiang, People's Republic of China.

Department of Radiology, The First Hospital of Jiaxing, Affiliated Hospital of Jiaxing University, Jiaxing, 314000, Zhejiang, People's Republic of China.

出版信息

Discov Oncol. 2025 Sep 26;16(1):1715. doi: 10.1007/s12672-025-03498-9.

DOI:10.1007/s12672-025-03498-9
PMID:41003937
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12474773/
Abstract

Colon adenocarcinoma (COAD) ranks among the most prevalent malignancies. C-type lectin domain family 11 member A (CLEC11A) plays a role in the initiation and progression of various cancers. However, its involvement in COAD remains unclear. This study reveals that CLEC11A expression is significantly elevated in COAD tissues compared to normal counterparts. Moreover, higher CLEC11A levels correlate with advanced T and N stages as well as pathological stage. Survival analysis further indicates that elevated CLEC11A expression is linked to poor prognosis. Cox regression analysis identifies CLEC11A as an independent prognostic factor for unfavorable survival outcomes. Additionally, increased CLEC11A expression shows a positive association with immune cell infiltration and immune checkpoint markers. CLEC11A-related differentially expressed genes (DEGs) were also identified, and functional enrichment analyses were conducted to elucidate the biological roles of CLEC11A. Unsupervised cluster analysis of these DEGs across distinct subgroups was also performed. In conclusion, CLEC11A has the potential as both a prognostic biomarker and a modulator of immune responses in COAD.

摘要

结肠腺癌(COAD)是最常见的恶性肿瘤之一。C型凝集素结构域家族11成员A(CLEC11A)在多种癌症的发生和发展中发挥作用。然而,其在COAD中的作用仍不清楚。本研究表明,与正常组织相比,COAD组织中CLEC11A的表达显著升高。此外,较高的CLEC11A水平与晚期T和N分期以及病理分期相关。生存分析进一步表明,CLEC11A表达升高与预后不良有关。Cox回归分析确定CLEC11A是生存结果不良的独立预后因素。此外,CLEC11A表达增加与免疫细胞浸润和免疫检查点标志物呈正相关。还鉴定了与CLEC11A相关的差异表达基因(DEG),并进行了功能富集分析以阐明CLEC11A的生物学作用。还对这些DEG在不同亚组中进行了无监督聚类分析。总之,CLEC11A有潜力作为COAD的预后生物标志物和免疫反应调节剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34bf/12474773/d653e81f0a08/12672_2025_3498_Figj_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34bf/12474773/f32abe27c2e9/12672_2025_3498_Figa_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34bf/12474773/e5a3fdcca0a5/12672_2025_3498_Figc_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34bf/12474773/dd63fcc33e83/12672_2025_3498_Figd_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34bf/12474773/6a2c2b07d752/12672_2025_3498_Fige_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34bf/12474773/2665c3991df3/12672_2025_3498_Figf_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34bf/12474773/a7b986581615/12672_2025_3498_Figh_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34bf/12474773/d653e81f0a08/12672_2025_3498_Figj_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34bf/12474773/f32abe27c2e9/12672_2025_3498_Figa_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34bf/12474773/e5a3fdcca0a5/12672_2025_3498_Figc_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34bf/12474773/dd63fcc33e83/12672_2025_3498_Figd_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34bf/12474773/6a2c2b07d752/12672_2025_3498_Fige_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34bf/12474773/2665c3991df3/12672_2025_3498_Figf_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34bf/12474773/a7b986581615/12672_2025_3498_Figh_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34bf/12474773/d653e81f0a08/12672_2025_3498_Figj_HTML.jpg

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本文引用的文献

1
The role of Clec11a in bone construction and remodeling.Clec11a 在骨骼构建和重塑中的作用。
Front Endocrinol (Lausanne). 2024 Aug 12;15:1429567. doi: 10.3389/fendo.2024.1429567. eCollection 2024.
2
STING agonist inflames the cervical cancer immune microenvironment and overcomes anti-PD-1 therapy resistance.STING 激动剂激活宫颈癌免疫微环境并克服抗 PD-1 治疗耐药性。
Front Immunol. 2024 Mar 14;15:1342647. doi: 10.3389/fimmu.2024.1342647. eCollection 2024.
3
Identification and characterization of CLEC11A and its derived immune signature in gastric cancer.
鉴定和表征胃癌中的 CLEC11A 及其衍生免疫特征。
Front Immunol. 2024 Jan 29;15:1324959. doi: 10.3389/fimmu.2024.1324959. eCollection 2024.
4
Expression of Concern: HER3, but Not HER4, Plays an Essential Role in the Clinicopathology and Prognosis of Gastric Cancer: A Meta-Analysis.
PLoS One. 2023 May 24;18(5):e0286446. doi: 10.1371/journal.pone.0286446. eCollection 2023.
5
CLEC11A improves insulin secretion and promotes cell proliferation in human beta-cells.CLEC11A 可改善人胰岛β细胞的胰岛素分泌功能并促进其增殖。
J Mol Endocrinol. 2023 Jun 21;71(1). doi: 10.1530/JME-22-0066. Print 2023 Jul 1.
6
Treatment with decitabine induces the expression of stemness markers, PD-L1 and NY-ESO-1 in colorectal cancer: potential for combined chemoimmunotherapy.地西他滨治疗诱导结直肠癌细胞干性标志物、PD-L1 和 NY-ESO-1 的表达:联合化疗免疫治疗的潜力。
J Transl Med. 2023 Mar 31;21(1):235. doi: 10.1186/s12967-023-04073-y.
7
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