Role of Colony Stimulating Factor 1 (CSF-1) and Its Receptor CSF1R: Macrophage Repolarization for Glioblastoma Treatment

IF 3.7 Q1 CHEMISTRY, MEDICINAL
Gaurisha alias Resha Ramnath Naik, , , Rachana S P, , , Sandesh Ramchandra Jadhav, , , Rahul Pokale, , , Paniz Hedayat, , , Deepanjan Datta, , , Bhupendra Prajapati, , , Srinivas Mutalik, , and , Namdev Dhas*, 
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引用次数: 0

Abstract

Glioblastoma multiforme (GBM) is the most aggressive and prevailing form of primary brain tumor, illustrated by its rapid growth and invasive nature. GBM continues to be highly incurable despite advancements in treatment due to its complex tumor microenvironment (TME) and the unique characteristics of tumor-associated macrophages (TAMs). This review explores the function of macrophages within the TME of GBM, specifically emphasizing the impact of colony-stimulating Factor-1 (CSF-1) and its receptor CSF1R in macrophage biology. The progression, survival, and differentiation of TAMs, which often rely on immunosuppressive properties that contribute to tumor growth and treatment resistance, are facilitated by elevated CSF-1 levels in GBM. The inhibition of CSF1R presents a promising therapeutic strategy, as it selectively targets tumor-promoting macrophages while sparing antitumor macrophages. Preclinical evidence demonstrates improved survival outcomes through CSF1R inhibition in mouse models, highlighting its potential for clinical application. Ongoing clinical trials further investigate this approach, aiming to enhance treatment efficacy for patients with GBM. This review concludes by emphasizing the significance of repolarizing macrophages as a novel therapeutic opportunity in GBM management, alongside emerging trends and future research directions that could lead to breakthroughs in treatment strategies.

集落刺激因子1 (CSF-1)及其受体CSF1R:巨噬细胞复极化在胶质母细胞瘤治疗中的作用
多形性胶质母细胞瘤(GBM)是原发性脑肿瘤中最具侵袭性和最普遍的形式,其快速生长和侵袭性表现出来。尽管治疗取得了进展,但由于其复杂的肿瘤微环境(TME)和肿瘤相关巨噬细胞(tam)的独特特征,GBM仍然是高度不可治愈的。本文综述了巨噬细胞在GBM TME中的功能,特别强调了集落刺激因子-1 (CSF-1)及其受体CSF1R在巨噬细胞生物学中的作用。TAMs的进展、生存和分化通常依赖于免疫抑制特性,从而促进肿瘤生长和治疗耐药性,而GBM中CSF-1水平的升高促进了TAMs的进展、生存和分化。抑制CSF1R是一种很有前景的治疗策略,因为它可以选择性地靶向促肿瘤巨噬细胞,同时保留抗肿瘤巨噬细胞。临床前证据表明,在小鼠模型中通过抑制CSF1R改善了生存结果,突出了其临床应用潜力。正在进行的临床试验进一步研究这种方法,旨在提高GBM患者的治疗效果。本文最后强调了复极化巨噬细胞作为GBM治疗的新治疗机会的重要性,以及可能导致治疗策略突破的新兴趋势和未来研究方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Pharmacology and Translational Science
ACS Pharmacology and Translational Science Medicine-Pharmacology (medical)
CiteScore
10.00
自引率
3.30%
发文量
133
期刊介绍: ACS Pharmacology & Translational Science publishes high quality, innovative, and impactful research across the broad spectrum of biological sciences, covering basic and molecular sciences through to translational preclinical studies. Clinical studies that address novel mechanisms of action, and methodological papers that provide innovation, and advance translation, will also be considered. We give priority to studies that fully integrate basic pharmacological and/or biochemical findings into physiological processes that have translational potential in a broad range of biomedical disciplines. Therefore, studies that employ a complementary blend of in vitro and in vivo systems are of particular interest to the journal. Nonetheless, all innovative and impactful research that has an articulated translational relevance will be considered. ACS Pharmacology & Translational Science does not publish research on biological extracts that have unknown concentration or unknown chemical composition. Authors are encouraged to use the pre-submission inquiry mechanism to ensure relevance and appropriateness of research.
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