Ma Li, Yang Hailang, Wu Shuwei, Wang Chunliang, Mei Jinhong
Department of Pathology, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Institute of Molecular Pathology, Nanchang University, Nanchang, China.
J Cancer. 2024 Aug 19;15(16):5425-5439. doi: 10.7150/jca.93112. eCollection 2024.
Dipeptidyl peptidase 7 (DPP7) is overexpressed in various tumors, but its role in colorectal cancer (CRC) remains unclear. Study the Impact of DPP7 on malignant progression and tumor immunity in CRC. We utilized Tumor Immune Estimation Resource 2.0 (TIMER2.0) and The Cancer Genome Atlas (TCGA) analyses to assess the expression of DPP7 in tumors and validated it through immunohistochemistry and immunoblotting. Additionally, we investigated the relationship between DPP7 and immune cell infiltration using single-sample Gene Set Enrichment Analysis (ssGSEA) analysis. Finally, the impact of DPP7 on cell proliferation, invasion, migration, and immune cell function in the tumor microenvironment was confirmed through cell experiments and animal studies. DPP7 is highly expressed in CRC, and high expression of DPP7 is associated with poor prognosis. Cell experiments demonstrate that overexpression of DPP7 enhances the proliferation, migration, and invasion capabilities of colorectal cancer cells both and . Immune infiltration analysis and co-culture results indicate that overexpression of DPP7 suppresses the immune cell's cytotoxic function against tumors in the tumor microenvironment. DPP7 promotes the malignant potential of colorectal cancer cells and inhibits tumor immune function, thereby promoting the progression of colorectal cancer.
二肽基肽酶7(DPP7)在多种肿瘤中过表达,但其在结直肠癌(CRC)中的作用仍不清楚。研究DPP7对CRC恶性进展和肿瘤免疫的影响。我们利用肿瘤免疫评估资源2.0(TIMER2.0)和癌症基因组图谱(TCGA)分析来评估肿瘤中DPP7的表达,并通过免疫组织化学和免疫印迹进行验证。此外,我们使用单样本基因集富集分析(ssGSEA)研究DPP7与免疫细胞浸润之间的关系。最后,通过细胞实验和动物研究证实了DPP7对肿瘤微环境中细胞增殖、侵袭、迁移和免疫细胞功能的影响。DPP7在CRC中高表达,且DPP7的高表达与不良预后相关。细胞实验表明,DPP7的过表达增强了结肠癌细胞的增殖、迁移和侵袭能力。免疫浸润分析和共培养结果表明,DPP7的过表达抑制了肿瘤微环境中免疫细胞对肿瘤的细胞毒性功能。DPP7促进结肠癌细胞的恶性潜能并抑制肿瘤免疫功能,从而促进结直肠癌的进展。