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王虎, 尹艳梅, 杜昊轩, 陈浩, 马小鹏, 戴爱斌, 朱克祥. MKI67在胰腺癌中的表达及临床意义[J]. 肿瘤防治研究, 2024, 51(2): 91-98. DOI: 10.3971/j.issn.1000-8578.2024.23.0762
引用本文: 王虎, 尹艳梅, 杜昊轩, 陈浩, 马小鹏, 戴爱斌, 朱克祥. MKI67在胰腺癌中的表达及临床意义[J]. 肿瘤防治研究, 2024, 51(2): 91-98. DOI: 10.3971/j.issn.1000-8578.2024.23.0762
WANG Hu, YIN Yanmei, DU Haoxuan, CHEN Hao, MA Xiaopeng, DAI Aibin, ZHU Kexiang. Expression and Clinical Significance of MKI67 in Pancreatic Cancer[J]. Cancer Research on Prevention and Treatment, 2024, 51(2): 91-98. DOI: 10.3971/j.issn.1000-8578.2024.23.0762
Citation: WANG Hu, YIN Yanmei, DU Haoxuan, CHEN Hao, MA Xiaopeng, DAI Aibin, ZHU Kexiang. Expression and Clinical Significance of MKI67 in Pancreatic Cancer[J]. Cancer Research on Prevention and Treatment, 2024, 51(2): 91-98. DOI: 10.3971/j.issn.1000-8578.2024.23.0762

MKI67在胰腺癌中的表达及临床意义

Expression and Clinical Significance of MKI67 in Pancreatic Cancer

  • 摘要:
    目的 探讨MKI67在胰腺癌中的表达、生物学功能、潜在机制及其临床意义。
    方法 利用公共数据库分析MKI67在胰腺癌中的表达水平、诊断和预后价值,研究MKI67与免疫细胞浸润和免疫检查点分子之间的关系,并通过功能通路的富集分析揭示其可能的分子机制。采用qRT-PCR和Western blot法验证MKI67在mRNA和蛋白质水平的表达,采用免疫组织化学染色对MKI67在组织蛋白的表达水平进行检测。
    结果 MKI67的高表达与胰腺癌较高的组织学分级和较差的预后显著相关。MKI67表达升高与胰腺癌患者不良预后相关(P=0.009),是影响患者预后的独立危险因素(95%CI: 1.084~1.743, P<0.05)。MKI67的表达与Th2细胞水平呈正相关,而与pDC细胞、NK细胞、肥大细胞、T滤泡辅助细胞、免疫DC和CD8+T细胞呈负相关。
    结论 MKI67可能作为胰腺癌的诊断和预后生物标志物,其机制可能与免疫逃逸或免疫抑制相关。

     

    Abstract:
    Objectives To explore the expression, biological function, and mechanism of MKI67 in pancreatic cancer and its clinical significance.
    Methods The expression level, diagnosis, and prognostic value of MKI67 in pancreatic cancer were analyzed using public databases. We also investigated the association between the MKI67 with immune cell infiltration and immune checkpoint molecules. We analyzed the functional pathway enrichment to uncover the possible molecular mechanisms. qRT-PCR and Western blot assay were used to verify the expression of MKI67 mRNA and protein. Immunohistochemistry staining was used to detect the expression of MKI67 in tissue protein.
    Results The high expression of MKI67 was significantly associated with high histological grades and poor outcomes in pancreatic cancer. High MKI67 expression was correlated with poor prognosis of pancreatic cancer patients (P=0.009). MKI67 was an independent risk factor for the patient outcome (95%CI: 1.084-1.743, P<0.05). The MKI67 expression was positively correlated with the helper T cell 2 levels but negatively correlated with plasmacytoid DC, NK cells, mast cells, the T follicular helper, immune DC, and CD8 T cells.
    Conclusion MKI67 may serve as a biomarker for the diagnosis and prognosis of pancreatic cancer and the mechanism might be associated with immune escape or immunosuppression.

     

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