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多组学分析揭示了PTPN6对多种癌症肿瘤免疫的影响。

Multi-omic analyses reveal PTPN6's impact on tumor immunity across various cancers.

作者信息

Zhong Yuchen, Zhang Weiyuan, Zheng Chaojing, Wu Hongyu, Luo Jun, Yuan Ziming, Zhang Hao, Wang Chunlin, Feng Haiyang, Wang Meng, Zhang Qian, Ju Haixing, Wang Guiyu

机构信息

Department of Colorectal Cancer Surgery, the Second Affiliated Hospital of Harbin Medical University, Harbin, 150000, Heilongjiang, People's Republic of China.

Department of Colorectal Cancer Surgery, Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences, Hangzhou, Zhejiang, People's Republic of China.

出版信息

Sci Rep. 2025 Apr 1;15(1):11025. doi: 10.1038/s41598-025-96302-1.

DOI:10.1038/s41598-025-96302-1
PMID:40164665
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11958644/
Abstract

Protein Tyrosine Phosphatase Non-Receptor Type 6 (PTPN6) plays a crucial regulatory role in cellular processes and has been implicated in oncogenesis. This pan-cancer analysis aimed to elucidate PTPN6's involvement across various cancer types, with a particular emphasis on its association with tumor immunity. We analyzed PTPN6 expression data from open access databases using various statistical techniques, including survival analysis, genetic heterogeneity analysis, immune profiling, single-cell analysis, drug sensitivity analysis, and protein interaction analysis. We also conducted in vitro experiments utilizing colorectal cancer cell lines to validate PTPN6's functional role. PTPN6 exhibited distinct expression patterns across cancers, and its prognostic significance was apparent in several cancer types, particularly in glioblastoma, sarcoma, and melanoma. We observed correlations between PTPN6 and immune genes/cell infiltration in these cancers, suggesting a potential role in modulating the tumor immune microenvironment. Single-cell analysis revealed that PTPN6 is predominantly localized in macrophages, B cells, and dendritic cells within the tumor microenvironment, implying its involvement in regulating immune cell function. Enrichment analysis highlighted PTPN6's role in immune-related pathways. Drug sensitivity analysis identified specific drugs, including PAC-1, SNX-2112, BELINOSTAT, VORINOSTAT, TPCA-1, and PHA-893,888, whose efficacy may be influenced by PTPN6 expression. Knocking down PTPN6 expression inhibited the proliferation and migration of colorectal cancer cells in vitro, confirming its oncogenic role in this cancer type. This pan-cancer analysis establishes PTPN6's multifaceted influence on tumor immunity and its potential as a biomarker and therapeutic target.

摘要

非受体型6蛋白酪氨酸磷酸酶(PTPN6)在细胞过程中发挥着关键的调节作用,并与肿瘤发生有关。这项泛癌分析旨在阐明PTPN6在各种癌症类型中的作用,尤其着重于其与肿瘤免疫的关联。我们使用了包括生存分析、基因异质性分析、免疫谱分析、单细胞分析、药物敏感性分析和蛋白质相互作用分析等各种统计技术,分析了来自开放获取数据库的PTPN6表达数据。我们还利用结肠癌细胞系进行了体外实验,以验证PTPN6的功能作用。PTPN6在不同癌症中呈现出不同的表达模式,其预后意义在几种癌症类型中很明显,特别是在胶质母细胞瘤、肉瘤和黑色素瘤中。我们观察到这些癌症中PTPN6与免疫基因/细胞浸润之间的相关性,表明其在调节肿瘤免疫微环境中可能发挥作用。单细胞分析显示,PTPN6主要定位于肿瘤微环境中的巨噬细胞、B细胞和树突状细胞内,这意味着它参与调节免疫细胞功能。富集分析突出了PTPN6在免疫相关途径中的作用。药物敏感性分析确定了包括PAC-1、SNX-2112、贝利司他、伏立诺他、TPCA-1和PHA-893,888在内的特定药物,其疗效可能受PTPN6表达的影响。敲低PTPN6表达可抑制结肠癌细胞在体外的增殖和迁移,证实了其在这种癌症类型中的致癌作用。这项泛癌分析确立了PTPN6对肿瘤免疫的多方面影响及其作为生物标志物和治疗靶点的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18f/11958644/7f05bb8e82a2/41598_2025_96302_Fig9_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18f/11958644/7f05bb8e82a2/41598_2025_96302_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18f/11958644/982ec06de416/41598_2025_96302_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18f/11958644/db67151c622d/41598_2025_96302_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18f/11958644/66ba9c2213d7/41598_2025_96302_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18f/11958644/339df87d1177/41598_2025_96302_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18f/11958644/cb1c977cc55d/41598_2025_96302_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18f/11958644/7f05bb8e82a2/41598_2025_96302_Fig9_HTML.jpg

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本文引用的文献

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Mechanism study of tyrosine phosphatase shp-1 in inhibiting hepatocellular carcinoma progression by regulating the SHP2/GM-CSF pathway in TAMs.
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Neurotransmitter Receptor HTR2B Regulates Lipid Metabolism to Inhibit Ferroptosis in Gastric Cancer.神经递质受体 HTR2B 通过调节脂质代谢抑制胃癌中的铁死亡。
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