دورية أكاديمية

Dual role of ARPC1B in regulating the network between tumor-associated macrophages and tumor cells in glioblastoma

التفاصيل البيبلوغرافية
العنوان: Dual role of ARPC1B in regulating the network between tumor-associated macrophages and tumor cells in glioblastoma
المؤلفون: Tianqi Liu, Chen Zhu, Xin Chen, Jianqi Wu, Gefei Guan, Cunyi Zou, Shuai Shen, Ling Chen, Peng Cheng, Wen Cheng, Anhua Wu
المصدر: OncoImmunology, Vol 11, Iss 1 (2022)
بيانات النشر: Taylor & Francis Group, 2022.
سنة النشر: 2022
المجموعة: LCC:Immunologic diseases. Allergy
LCC:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
مصطلحات موضوعية: arpc1b, actin cytoskeleton, tam, macrophage, gbm, Immunologic diseases. Allergy, RC581-607, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
الوصف: The tumor microenvironment (TME) plays a critical role in promoting the growth and metastasis of glioblastoma (GBM). Tumor-associated macrophages (TAMs), the most abundant myeloid cells infiltrating in TME, produce proinflammatory cytokines, regulate glioma cell pools, and lead to GBM progression. Understanding the mechanism of GBM-TAMs regulation can help to find new targeted therapeutic strategies against GBM. Based on the CGGA and TCGA GBM cohorts, ARPC1B was defined as the key macrophage-associated gene with prognostic value. Higher ARPC1B expression was associated with progressive malignancy, poor outcomes and TAM infiltration. We demonstrated that macrophage-expressed ARPC1B promoted the migration, invasion, and epithelial–mesenchymal transition of glioma cells. Glioma-intrinsic ARPC1B also maintained the malignant phenotype and promoted macrophage recruitment. Positive feedback signaling between macrophages and glioma cells via ARPC1B was determined to be under control of the IFNγ-IRF2-ARPC1B axis. This study highlights the important role of ARPC1B in GBM malignancy progression and the regulation network between GBM and TAMs, suggesting ARPC1B as a novel biomarker with potential therapeutic implications.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2162-402X
2162402X
84105976
Relation: https://doaj.org/toc/2162-402X
DOI: 10.1080/2162402X.2022.2031499
URL الوصول: https://doaj.org/article/155484fd6fa841059763d5024f0fefc1
رقم الأكسشن: edsdoj.155484fd6fa841059763d5024f0fefc1
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:2162402X
84105976
DOI:10.1080/2162402X.2022.2031499