非常规 T 细胞在泌尿系统肿瘤中:能抓住就抓住
Unconventional T cells in urological cancers: catch them if you can.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Pyroptosis-Related Patterns Predict Tumor Immune Landscape and Immunotherapy Response in Bladder Cancer.
Pyroptosis-Related Patterns Predict Tumor Immune Landscape and Immunotherapy Response in Bladder Cancer.
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膀胱癌(BC)是恶性肿瘤致死的主要原因之一,晚期状态的免疫治疗反应存在显著异质性。细胞焦亡是一种新发现的炎症性程序性细胞死亡,已被证实其在肿瘤发生和抗肿瘤活性中发挥不可或缺的作用。然而,细胞焦亡对BC肿瘤免疫景观重塑和免疫治疗的影响仍不清楚。
我们全面评估了BC中33个细胞焦亡相关基因(PRGs)的mRNA表达和基因组改变,并在公开可用的BC数据集中评估了细胞焦亡模式。采用无监督聚类方法将患者分为不同的模式。然后,我们使用主成分分析建立了一个细胞焦亡相关特征评分(PS-score)模型,以量化个体BC患者的细胞焦亡相关模式。此外,我们将这些模式与免疫景观和免疫治疗反应疗效进行了关联分析。
在BC中鉴定出两种细胞焦亡相关模式,不同模式表现出不同的免疫特征。PRGs高表达水平的模式表现出生存优势,并显示更高的细胞毒性淋巴细胞浸润。PS-score低的肿瘤以高TIL(肿瘤浸润淋巴细胞)为特征,被认为是“热”肿瘤。进一步分析显示,PS-score是一个独立预后因素,并且可以预测晚期BC患者的免疫治疗反应。我们发现AHNAK2,即AHNAK核蛋白2,表达与PS-score之间存在显著正相关。功能实验表明,AHNAK2敲低与侵袭能力减弱相关。
本研究全面展示了焦亡相关模式在膀胱肿瘤免疫景观中的潜在功能,并确定了其在免疫治疗中的治疗价值。我们的研究加深了对免疫景观的理解,并为更有效的免疫治疗策略提供了新途径。
Background: Bladder cancer (BC) is a leading cause of death from malignancy, with significant heterogeneity in the immunotherapeutic responsiveness of advanced status. Pyroptosis, a newly discovered inflammatory programmed cell death, is confirmed to play an indispensable role in tumorigenesis and anti-tumor activity.
However, the effect of pyroptosis on the tumor-immune landscape remodeling and immunotherapy in BC remains elusive. Methods: We comprehensively evaluated the mRNA expression and genomic alterations of 33 pyroptosis-related genes (PRGs) in BC and evaluated the patterns of pyroptosis in publicly available BC datasets.
An unsupervised clustering method was used to classify patients into distinct patterns. Then, we established a pyroptosis-related signature score (PS-score) model to quantify the pyroptosis-related patterns of individual BC patients using principal component analysis.
Furthermore, we correlated the patterns with the immune landscape and response efficacy of immunotherapy. Results: Two pyroptosis-related patterns were identified in BC, and distinct patterns showed various immune characteristics. Patterns with a high expression level of PRGs exhibited a survival advantage and showed higher infiltration of cytotoxic lymphocytes. Tumors with a low PS-score were characterized by high tumor-infiltrating lymphocytes and considered "hot."
Further analysis revealed that the PS-score was an independent prognostic factor and could predict the response to immunotherapy for patients with advanced BC.
We found a significant positive association between AHNAK2, AHNAK nucleoprotein 2, expression, and PS-score. Functional assays showed that AHNAK2 knockdown was correlated with attenuated invasive ability. Conclusion: This work comprehensively demonstrated the potential function of pyroptosis-related patterns in the bladder tumor-immune landscape and identified their therapeutic liability in immunotherapy.
Our study enhanced our understanding of the immune landscape and provided a new approach toward more effective immunotherapy strategies.
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