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通过抑制单羧酸转运蛋白1(MCT1)或单羧酸转运蛋白4(MCT4)靶向乳酸代谢会损害白血病细胞增殖,诱导两种不同的相关死亡途径,并增加急性髓系白血病细胞的化疗敏感性。

Targeting Lactate Metabolism by Inhibiting MCT1 or MCT4 Impairs Leukemic Cell Proliferation, Induces Two Different Related Death-Pathways and Increases Chemotherapeutic Sensitivity of Acute Myeloid Leukemia Cells.

作者信息

Saulle Ernestina, Spinello Isabella, Quaranta Maria Teresa, Pasquini Luca, Pelosi Elvira, Iorio Egidio, Castelli Germana, Chirico Mattea, Pisanu Maria Elena, Ottone Tiziana, Voso Maria Teresa, Testa Ugo, Labbaye Catherine

机构信息

National Center for Drug Research and Evaluation, Istituto Superiore di Sanità, Rome, Italy.

Core Facilities, Istituto Superiore di Sanità, Rome, Italy.

出版信息

Front Oncol. 2021 Feb 5;10:621458. doi: 10.3389/fonc.2020.621458. eCollection 2020.

Abstract

Metabolism in acute myeloid leukemia (AML) cells is dependent primarily on oxidative phosphorylation. However, in order to sustain their high proliferation rate and metabolic demand, leukemic blasts use a number of metabolic strategies, including glycolytic metabolism. Understanding whether monocarboxylate transporters MCT1 and MCT4, which remove the excess of lactate produced by cancer cells, represent new hematological targets, and whether their respective inhibitors, AR-C155858 and syrosingopine, can be useful in leukemia therapy, may reveal a novel treatment strategy for patients with AML. We analyzed MCT1 and MCT4 expression and function in hematopoietic progenitor cells from healthy cord blood, in several leukemic cell lines and in primary leukemic blasts from patients with AML, and investigated the effects of AR-C155858 and syrosingopine, used alone or in combination with arabinosylcytosine, on leukemic cell proliferation. We found an inverse correlation between MCT1 and MCT4 expression levels in leukemic cells, and showed that MCT4 overexpression is associated with poor prognosis in AML patients. We also found that AR-C155858 and syrosingopine inhibit leukemic cell proliferation by activating two different cell-death related pathways, i.e., necrosis for AR-C155858 treatment and autophagy for syrosingopine, and showed that AR-C155858 and syrosingopine exert an anti-proliferative effect, additive to chemotherapy, by enhancing leukemic cells sensitivity to chemotherapeutic agents. Altogether, our study shows that inhibition of MCT1 or MCT4 impairs leukemic cell proliferation, suggesting that targeting lactate metabolism may be a new therapeutic strategy for AML, and points to MCT4 as a potential therapeutic target in AML patients and to syrosingopine as a new anti-proliferative drug and inducer of autophagy to be used in combination with conventional chemotherapeutic agents in AML treatment.

摘要

急性髓系白血病(AML)细胞的代谢主要依赖于氧化磷酸化。然而,为了维持其高增殖率和代谢需求,白血病原始细胞会采用多种代谢策略,包括糖酵解代谢。了解负责清除癌细胞产生的过量乳酸的单羧酸转运蛋白MCT1和MCT4是否代表新的血液学靶点,以及它们各自的抑制剂AR-C155858和毒毛旋花子苷是否可用于白血病治疗,可能会揭示一种针对AML患者的新治疗策略。我们分析了健康脐带血造血祖细胞、几种白血病细胞系以及AML患者的原发性白血病原始细胞中MCT1和MCT4的表达及功能,并研究了单独使用或与阿糖胞苷联合使用的AR-C155858和毒毛旋花子苷对白血病细胞增殖的影响。我们发现白血病细胞中MCT1和MCT4的表达水平呈负相关,并表明MCT4过表达与AML患者的不良预后相关。我们还发现,AR-C155858和毒毛旋花子苷通过激活两种不同的细胞死亡相关途径抑制白血病细胞增殖,即AR-C155858处理诱导坏死,毒毛旋花子苷诱导自噬,并表明AR-C155858和毒毛旋花子苷通过增强白血病细胞对化疗药物的敏感性发挥抗增殖作用,这种作用与化疗相加。总之,我们的研究表明,抑制MCT1或MCT4会损害白血病细胞增殖,提示靶向乳酸代谢可能是AML的一种新治疗策略,并指出MCT4是AML患者的潜在治疗靶点,毒毛旋花子苷是一种新的抗增殖药物和自噬诱导剂,可与AML治疗中的传统化疗药物联合使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f08/7892602/cdd403025592/fonc-10-621458-g001.jpg

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