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用一种受生物启发的配体靶向清道夫受体B1类可诱导急性髓系白血病细胞凋亡或铁死亡。

Targeting scavenger receptor class B type 1 with a bioinspired ligand induces apoptosis or ferroptosis in AML.

作者信息

Lin Adam Y, Rink Jonathan S, Yang Eva, Small Sara, Gerber Jessica J, Zak Taylor J, Altman Jessica, Abaza Yasmin, Platanias Leonidas C, Gordon Leo I, Thaxton C Shad

机构信息

Division of Hematology/Oncology, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL.

Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL.

出版信息

Blood Neoplasia. 2025 Jun 3;2(4):100122. doi: 10.1016/j.bneo.2025.100122. eCollection 2025 Nov.

Abstract

Despite progress in research and treatment strategies for acute myeloid leukemia (AML), the prognosis for patients with AML, particularly for individuals aged >60 years and those with adverse risk factors, remains poor. Cellular receptors that affect cholesterol homeostasis may present a new target for treating AML. Scavenger receptor class B type 1 (SR-B1), which plays an important role in cellular cholesterol uptake and redox balance, is expressed by AML cells and correlates with poor patient outcomes. Previously, we targeted SR-B1 in various hematologic and solid malignancies with a synthetic bioinspired high-density lipoprotein nanoparticle (HDL NP) ligand that disrupted cholesterol metabolism, inhibited protective antioxidant mechanisms, and induced ferroptosis. This study demonstrates that HDL NPs are effective at low nanomolar drug concentrations in AML, surpassing the effectiveness of cytarabine, a standard-of-care chemotherapy agent. The HDL NP reduced glutathione peroxidase 4, leading to reactive oxygen species accumulation, which causes some AML cells to undergo ferroptosis while others undergo apoptosis and pyroptosis. HDL NP treatment was synergistic with standard AML therapies, including cytarabine, venetoclax, and gilteritinib for fms-like tyrosine kinase 3-mutated leukemia cells. Notably, HDL NP treatment induced the differentiation of AML cells into mature granulocytes. Overall, this study provides a foundation for further investigations into the underlying mechanisms and clinical applications of SR-B1 targeting in AML treatment.

摘要

尽管急性髓系白血病(AML)的研究和治疗策略取得了进展,但AML患者的预后仍然很差,尤其是60岁以上的个体以及具有不良风险因素的患者。影响胆固醇稳态的细胞受体可能成为治疗AML的新靶点。清道夫受体B1型(SR-B1)在细胞胆固醇摄取和氧化还原平衡中起重要作用,AML细胞表达该受体,且与患者不良预后相关。此前,我们用一种合成的仿生高密度脂蛋白纳米颗粒(HDL NP)配体靶向SR-B1,该配体可破坏胆固醇代谢、抑制保护性抗氧化机制并诱导铁死亡,用于治疗各种血液系统和实体恶性肿瘤。本研究表明,HDL NPs在AML中低纳摩尔药物浓度下有效,超过了护理标准化疗药物阿糖胞苷的有效性。HDL NP降低了谷胱甘肽过氧化物酶4,导致活性氧积累,这使得一些AML细胞发生铁死亡,而另一些细胞则发生凋亡和焦亡。HDL NP治疗与标准AML疗法具有协同作用,包括阿糖胞苷、维奈克拉和针对FMS样酪氨酸激酶3突变白血病细胞的吉列替尼。值得注意的是,HDL NP治疗可诱导AML细胞分化为成熟粒细胞。总体而言,本研究为进一步研究SR-B1靶向治疗AML的潜在机制和临床应用奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4803/12418828/0260d62818ea/BNEO_NEO-2024-000469-ga1.jpg

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