Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, China.
Graduate School, Beijing University of Chinese Medicine, Beijing, China.
Technol Cancer Res Treat. 2024 Jan-Dec;23:15330338241281285. doi: 10.1177/15330338241281285.
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. 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. 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. 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.
肝素酶 (HPSE) 是一种内切糖苷酶,可切割肝素硫酸,调节与肿瘤进展相关的各种生物学过程。我们探讨了 HPSE 在乳腺癌患者中的预后价值及其与免疫治疗反应的关系,以提高免疫治疗的效果并增加生存结果。
在研究中,我们通过癌症基因组图谱 (TCGA) 数据库探讨了 HPSE 的预后价值。通过使用单样本基因集富集分析 (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 (CTRP) 和 PRISM 数据集提供了测量药物敏感性的剂量反应曲线下面积 (AUC)。使用列线图预测总体生存能力。在体内研究中,我们通过对小鼠三阴性乳腺癌肿瘤进行免疫组织化学研究,研究了 HPSE 与免疫检查点蛋白和促炎细胞因子之间的关系。
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,突出高 HPSE 表达是乳腺癌的预后危险因素。然后,受试者工作特征 (ROC) 曲线 [1 年 AUC=0.747,3 年 AUC=0.731] 和决策曲线分析 (DCA) 曲线表明我们的模型具有令人满意的区分能力,强调了其在临床应用中的价值。免疫相关结果表明,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,并且与促炎细胞因子 TNF-α呈正相关。同时,我们分析了对 HPSE 基因敏感的 11 种类型的药物。
我们的结果表明,HPSE 可以作为预测乳腺癌患者预后的有效生物标志物,并反映免疫治疗的影响。