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线粒体丙酮酸载体复合物增强了多发性骨髓瘤中蛋白酶体抑制剂的疗效。

The mitochondrial pyruvate carrier complex potentiates the efficacy of proteasome inhibitors in multiple myeloma.

机构信息

Lady Davis Institute for Medical Research, Segal Cancer Centre, Jewish General Hospital, Montreal, Canada.

Division of Experimental Medicine, McGill University, Montreal, Canada.

出版信息

Blood Adv. 2023 Jul 25;7(14):3485-3500. doi: 10.1182/bloodadvances.2022008345.

Abstract

Multiple myeloma (MM) is a hematological malignancy that emerges from antibody-producing plasma B cells. Proteasome inhibitors, including the US Food and Drug Administration-approved bortezomib (BTZ) and carfilzomib (CFZ), are frequently used for the treatment of patients with MM. Nevertheless, a significant proportion of patients with MM are refractory or develop resistance to this class of inhibitors, which represents a significant challenge in the clinic. Thus, identifying factors that determine the potency of proteasome inhibitors in MM is of paramount importance to bolster their efficacy in the clinic. Using genome-wide CRISPR-based screening, we identified a subunit of the mitochondrial pyruvate carrier (MPC) complex, MPC1, as a common modulator of BTZ response in 2 distinct human MM cell lines in vitro. We noticed that CRISPR-mediated deletion or pharmacological inhibition of the MPC complex enhanced BTZ/CFZ-induced MM cell death with minimal impact on cell cycle progression. In fact, targeting the MPC complex compromised the bioenergetic capacity of MM cells, which is accompanied by reduced proteasomal activity, thereby exacerbating BTZ-induced cytotoxicity in vitro. Importantly, we observed that the RNA expression levels of several regulators of pyruvate metabolism were altered in advanced stages of MM for which they correlated with poor patient prognosis. Collectively, this study highlights the importance of the MPC complex for the survival of MM cells and their responses to proteasome inhibitors. These findings establish mitochondrial pyruvate metabolism as a potential target for the treatment of MM and an unappreciated strategy to increase the efficacy of proteasome inhibitors in the clinic.

摘要

多发性骨髓瘤(MM)是一种血液恶性肿瘤,起源于产生抗体的浆细胞。蛋白酶体抑制剂,包括美国食品和药物管理局批准的硼替佐米(BTZ)和卡非佐米(CFZ),常用于治疗 MM 患者。然而,相当一部分 MM 患者对此类抑制剂具有耐药性或产生耐药性,这在临床上是一个重大挑战。因此,确定决定蛋白酶体抑制剂在 MM 中效力的因素对于增强其在临床上的疗效至关重要。通过基于全基因组 CRISPR 的筛选,我们在 2 种不同的人 MM 细胞系中鉴定出线粒体丙酮酸载体(MPC)复合物的亚基 MPC1 是 BTZ 反应的常见调节剂。我们注意到,CRISPR 介导的 MPC 复合物缺失或药理学抑制增强了 BTZ/CFZ 诱导的 MM 细胞死亡,而对细胞周期进程的影响最小。事实上,靶向 MPC 复合物会损害 MM 细胞的生物能量能力,伴随着蛋白酶体活性降低,从而在体外加剧 BTZ 诱导的细胞毒性。重要的是,我们观察到几种丙酮酸代谢调节剂的 RNA 表达水平在 MM 的晚期阶段发生改变,它们与患者预后不良相关。总的来说,这项研究强调了 MPC 复合物对于 MM 细胞存活及其对蛋白酶体抑制剂反应的重要性。这些发现将线粒体丙酮酸代谢确立为治疗 MM 的潜在靶点,并为提高蛋白酶体抑制剂在临床上的疗效提供了一种未被认识的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a6a/10362273/c413f043057a/BLOODA_ADV-2022-008345-fx1.jpg

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