Agrimol B induces apoptosis and ferroptosis in acute monocytic leukemia by targeting EGFR/ERK1/2 signaling and activating SIRT1

IF 3.5 Q3 Medicine
Ting Ma, Qi Wang, Hao Wang, Ke Li, Dan Zhao, Wenjie Huang, Tao Li, Dantong Lyu, Hong Hong, Yue Liu, Min Wang, Jiuqing Gao, Xin Meng, Haiyan Zhang, Xu Wang, Bin Wu
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引用次数: 0

Abstract

Leukemia is an aggressive hematologic malignancy with high global morbidity and mortality. Despite advances in CAR-T cell therapy and targeted treatments, acute myeloid leukemia and high-risk relapsed cases continue to face formidable therapeutic challenges owing to heterogeneity and drug resistance. Agrimol B (AB), a bioactive natural compound isolated from the edible and medicinal plant Agrimonia pilosa Ledeb., has demonstrated notable anticancer potential. However, its role in leukemia has not yet been investigated. Here, we demonstrate that AB significantly reduces leukemia burden in an Acute Monocytic Leukemia (AMoL) mouse model and suppresses proliferation, invasion, and migration of THP-1 cells in vitro. Mechanistically, AB interacts with EGFR and inhibits ERK1/2 signaling, thereby activating FOXO1. In addition, AB upregulates SIRT1 expression and promotes FOXO1 deacetylation, leading to HMOX1 activation and subsequently triggers ferroptosis. These findings indicate that Agrimol B exerts potent anti-leukemic activity through multiple mechanisms, highlighting its potential as a therapeutic candidate for AMoL.
Agrimol B通过靶向EGFR/ERK1/2信号通路和激活SIRT1诱导急性单核细胞白血病细胞凋亡和铁凋亡。
白血病是一种侵袭性血液系统恶性肿瘤,全球发病率和死亡率都很高。尽管CAR-T细胞疗法和靶向治疗取得了进展,但由于异质性和耐药,急性髓系白血病和高危复发病例仍然面临着巨大的治疗挑战。Agrimol B (AB)是一种从药用和食用植物Agrimonia pilosa Ledeb中分离得到的具有生物活性的天然化合物。已经显示出显著的抗癌潜力。然而,它在白血病中的作用尚未被研究。本研究表明,AB可显著降低急性单核细胞白血病(AMoL)小鼠模型的白血病负担,并在体外抑制THP-1细胞的增殖、侵袭和迁移。在机制上,AB与EGFR相互作用,抑制ERK1/2信号,从而激活fox01。此外,AB上调SIRT1表达,促进FOXO1去乙酰化,导致HMOX1激活,进而引发铁下垂。这些发现表明,Agrimol B通过多种机制发挥强大的抗白血病活性,突出了其作为AMoL治疗候选药物的潜力。
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来源期刊
CiteScore
4.30
自引率
0.00%
发文量
148
审稿时长
56 days
期刊介绍: Cancer Treatment and Research Communications is an international peer-reviewed publication dedicated to providing comprehensive basic, translational, and clinical oncology research. The journal is devoted to articles on detection, diagnosis, prevention, policy, and treatment of cancer and provides a global forum for the nurturing and development of future generations of oncology scientists. Cancer Treatment and Research Communications publishes comprehensive reviews and original studies describing various aspects of basic through clinical research of all tumor types. The journal also accepts clinical studies in oncology, with an emphasis on prospective early phase clinical trials. Specific areas of interest include basic, translational, and clinical research and mechanistic approaches; cancer biology; molecular carcinogenesis; genetics and genomics; stem cell and developmental biology; immunology; molecular and cellular oncology; systems biology; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; cancer policy; and integration of various approaches. Our mission is to be the premier source of relevant information through promoting excellence in research and facilitating the timely translation of that science to health care and clinical practice.
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