CD81 通过阻断 CD274/PD-L1 的选择性自噬降解驱动放射抵抗性胶质母细胞瘤的免疫逃逸
CD81 drives immune evasion in radioresistant glioblastoma by blocking selective autophagic degradation of CD274/PD-L1.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Turning attention to tumor-host interface and focus on the peritumoral heterogeneity of glioblastoma.
Turning attention to tumor-host interface and focus on the peritumoral heterogeneity of glioblastoma.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
大约90%的胶质母细胞瘤复发发生在瘤周脑区(PBZ),而PBZ的空间异质性尚未得到充分研究。在本研究中,通过术前影像学从每位患者获取两个PBZ组织和一个肿瘤组织样本。我们使用多种技术评估微环境以及浸润免疫/肿瘤细胞的特征。我们的数据表明,PBZ中存在一个或多个脑血流量较高的区域,我们将其统称为“高脑血流量界面”(HBI)。HBI表现出比“低脑血流量界面”(LBI)更多的新生血管形成。与LBI相比,HBI往往有更多的巨噬细胞和T淋巴细胞浸润。HBI中的肿瘤细胞多于LBI,且这些肿瘤细胞的基因表达谱存在显著差异。HBI可能是手术切除后PBZ靶向治疗的关键区域。
Approximately 90% of glioblastoma recurrences occur in the peritumoral brain zone (PBZ), while the spatial heterogeneity of the PBZ is not well studied. In this study, two PBZ tissues and one tumor tissue sample are obtained from each patient via preoperative imaging.
We assess the microenvironment and the characteristics of infiltrating immune/tumor cells using various techniques.
Our data indicate there are one or more regions with higher cerebral blood flow in PBZ, which we collectively name the "higher cerebral blood flow interface" (HBI). The HBI exhibited more neovascularization than the "lower cerebral blood flow interfaces" (LBI).
The HBI tend to have increased infiltration of macrophages and T lymphocytes infiltration compared with that in LBI. There are more tumor cells in the HBI than in LBI, with substantial differences in the gene expression profiles of these tumor cells. HBI may be the key area of PBZ-targeting therapy after surgical resection.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。