通过 CD274/CTLA-4 免疫检查点蛋白分析肝素酶在乳腺癌中的表达模式和预后价值

IF 2.7 4区 医学 Q3 ONCOLOGY Technology in Cancer Research & Treatment Pub Date : 2024-01-01 DOI:10.1177/15330338241281285
Weijia Kong, Ganlin Zhang, Yue Wang, Jiahui Zhang, Tongjing Ding, Dong Chen, Yuancan Pan, Runxi Yi, Xiaohui Yin, Xiaomin Wang
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引用次数: 0

摘要

目的:肝素酶(HPSE)是一种能裂解硫酸肝素的内糖苷酶,它能调节与肿瘤进展相关的各种生物过程。我们探讨了 HPSE 的预后价值及其与乳腺癌患者免疫治疗反应的关系,以改善免疫治疗的效果并提高生存率。研究方法在本研究中,我们通过癌症基因组图谱(TCGA)数据库探讨了HPSE的预后价值。通过单样本基因组富集分析(ssGSEA)方法,我们测量了肿瘤微环境中24种免疫细胞类型的浸润水平。癌症治疗反应门户网站(CTRP)和PRISM数据集提供了剂量反应曲线下面积(AUC),用于测量药物敏感性。利用提名图,我们预测了总体生存能力。在体内研究中,我们通过小鼠三阴性乳腺癌肿瘤的免疫组化研究了 HPSE 与免疫检查点蛋白和促炎细胞因子之间的关系。结果我们的模型表明,将 HPSE 与临床分期相结合可有效预测患者的生存时间,突出了高 HPSE 表达是乳腺癌的预后风险因素。随后的接收者操作特征曲线(ROC)[1年的AUC=0.747,3年的AUC=0.731]和决策曲线分析(DCA)曲线说明了我们的模型具有令人满意的鉴别能力,强调了其宝贵的临床应用价值。免疫相关结果显示,HPSE 与免疫浸润细胞、免疫相关基因和抗癌免疫周期密切相关。体内研究表明,乳腺癌中的HPSE与免疫检查点蛋白CD274和细胞毒性T淋巴细胞相关蛋白4(CTLA-4)的表达增加有关,并与促炎细胞因子TNF-α呈正相关。同时,我们分析了对 HPSE 基因敏感的 11 种药物。结论我们的研究结果表明,HPSE可作为一种有效的生物标志物来预测乳腺癌患者的预后并反映免疫疗法的影响。
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Analysis of Expression Pattern and Prognostic Value of the Heparanase in Breast Cancer Through CD274/CTLA-4 Immune Checkpoint Proteins.

Objectives: Heparanase (HPSE), an endoglycosidase that cleaves heparan sulfate, regulates various biological processes related to tumor progression. We explore the prognostic value of HPSE and its relationship with immunotherapy response in patients with breast cancer, to improve the effectiveness of immunotherapy and increase the survival outcomes. Methods: In the study, we explored the prognostic value of HPSE through the The Cancer Genome Atlas (TCGA) database. By using the single-sample gene set enrichment analysis (ssGSEA) method, we measured the infiltration levels of 24 immune cell types in the tumor microenvironment. Cancer Therapeutics Response Portal (CTRP) and PRISM datasets provide the area under the dose-response curve (AUC) to measure drug sensitivity. Using nomograms, we predicted overall survival ability. In vivo studies, we investigated the relationship between HPSE and immune checkpoint proteins and pro-inflammatory cytokines by immunohistochemistry of Triple-Negative Breast Cancer tumors in mice. Results: Our model demonstrated that the integrating of HPSE with the clinical stage effectively predicts patients' survival time, highlighting high HPSE expression as a prognostic risk factor for breast cancer. Then the Receiver Operating Characteristic (ROC) curve [AUC of 1 year = 0.747, AUC of 3 years = 0.731] and Decision Curve Analysis (DCA) curve illustrated the satisfactory discriminative capacity of our model, emphasizing its valuable clinical applicability. Immune-related results showed that HPSE correlates strongly with immune infiltrating cells, immune-related genes, and the anti-cancer immunity cycle. In vivo studies have demonstrated that HPSE in breast cancer is associated with increased expression of immune checkpoint proteins CD274 and cytotoxic T lymphocyte-associated protein 4 (CTLA-4) and is positively correlated with the pro-inflammatory cytokine TNF-α. Meanwhile, we analyzed the 11 types of drugs that are sensitive to the HPSE gene. Conclusion: Our results show that HPSE can serve as an effective biomarker to predict the prognosis of breast cancer patients and reflect the impact of immunotherapy.

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来源期刊
CiteScore
4.40
自引率
0.00%
发文量
202
审稿时长
2 months
期刊介绍: Technology in Cancer Research & Treatment (TCRT) is a JCR-ranked, broad-spectrum, open access, peer-reviewed publication whose aim is to provide researchers and clinicians with a platform to share and discuss developments in the prevention, diagnosis, treatment, and monitoring of cancer.
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