دورية أكاديمية
Dual role of ARPC1B in regulating the network between tumor-associated macrophages and tumor cells in glioblastoma
العنوان: | Dual role of ARPC1B in regulating the network between tumor-associated macrophages and tumor cells in glioblastoma |
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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 |
تدمد: | 2162402X 84105976 |
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DOI: | 10.1080/2162402X.2022.2031499 |