Fatty acid metabolism regulates ferroptosis in mutant KRAS lung cancer

脂肪酸代谢调节突变 KRAS 肺癌的铁死亡

基本信息

批准号：
10544159
负责人：
PIER Paolo SCAGLIONI
金额：
$ 39.4万
依托单位：
UNIVERSITY OF CINCINNATI
依托单位国家：
美国
项目类别：
财政年份：
2022
资助国家：
美国
起止时间：
2022-01-01 至 2026-12-31
项目状态：
未结题

来源：
https://reporter.nih.gov/project-details/10544159
关键词：
Acyl Coenzyme A Acylation Acyltransferase Affect Apoptosis Biochemical Pathway Bioenergetics Cancer Etiology Cancer cell line Cell Death Cell Survival Cell physiology Cells Cessation of life Coenzyme A Coenzyme A Ligases Data Dependence Development Drug Targeting Enzymes Essential Fatty Acids Esters Extinction Family member Fatty Acids Fatty-acid synthase Goals Growth Guanosine Triphosphate Phosphohydrolases Human Image Immunotherapy In Vitro Intracellular Accumulation of Lipids Iron Knowledge Lead Lecithin Lipid Peroxides Lysophosphatidylcholines Maintenance Malignant Neoplasms Malignant neoplasm of lung Metabolic Metabolism Minority Modeling Mutation Non-Small-Cell Lung Carcinoma Nonesterified Fatty Acids Oncogenes Oncogenic Oral Outcome Oxidative Stress PLA2G4C gene Patients Peroxides Phase II Clinical Trials Phenotype Phospholipase A2 Phospholipids Pre-Clinical Model Process Prognosis Proliferating Property Proto-Oncogenes Reaction Reactive Oxygen Species Resolution Role Signal Transduction Specimen Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization Testing Therapeutic Transgenic Mice Validation airway epithelium antitumor effect cancer cell cancer therapy coping effective therapy experimental study fatty acid metabolism feeding in vivo inhibitor innovation insight lipid metabolism lipidome lipidomics long chain fatty acid lung cancer cell lung tumorigenesis mouse model mutant novel novel therapeutics peroxidation reconstitution repaired tandem mass spectrometry therapeutic target therapy resistant tumor tumorigenesis

项目摘要

SUMMARY Lung cancer (LC) is the leading cause of cancer related death in the USA and in the world. Activating mutations of the proto-oncogene KRAS (mutant KRAS, KM thereafter) occur in ~30% of non-small cell lung cancer (NSCLC). These cancers are associated with an aggressive phenotype, resistance to therapy and poor outcome. Expression of KM in the respiratory epithelium is sufficient to initiate lung tumorigenesis. Furthermore, KM is required for the maintenance of established tumors. These observations establish KM as a high priority drug target. Only a minority of patients with KM-driven LC benefit from therapy, including immunotherapy or KRASG12C inhibitors. Accordingly, patients with KMLC have a poor prognosis. Hence, there is an urgent need for effective therapies for KMLC. Cancer cells undergo oncogene-directed metabolic reprogramming in order to meet the energetic and biosynthetic challenges of cell survival, growth and proliferation. It has been proposed that these changes are critical for the maintenance of established cancers. Indeed, we found that extinction of KM in LC of transgenic mice leads to the perturbation of several metabolic networks including fatty acid (FA) synthesis. To determine the contribution of lipid metabolism to KM-driven LC, we characterized the lipidome of KMLC with high resolution mass spectrometry, matrix-assisted laser desorption/ionization imaging MS (MALDI-IMS) and functional experiments. Our preliminary data indicate that KM upregulates Fatty acid synthase (FASN) and the synthesis of FA to repair peroxided phospholipids (PL) damaged by reactive oxygen species (ROS). FASN is often upregulated in cancer, however its role has remained elusive. We found that inhibition of FASN with TVB-3664, a first in class FASN inhibitor (FASNi), induces ferroptosis, a form of iron- and ROS- dependent programmed cell death characterized by the accumulation of lipid peroxides both in vitro and in vivo in preclinical models of KMLC. Lipidomics analysis and functional experiments suppressing ACSL3, LPCAT3 and PLA2G4C strongly suggest that in KMLC, FA serve a prosurvival function by feeding the Lands cycle, the main process that remodels the peroxided acyl chains of PL, deflecting ferroptosis. These observations support the hypothesis that KMLC depends on FA to evade ferroptosis and to promote tumorigenesis. We propose to test this hypothesis with a multifaceted approach that employs KM transgenic mice, panels of LC cells lines, functional and lipidomics experiments. it is worth noting that our group provided the rationale for a phase II clinical trial of TVB-2640, a FASNi derivative, in patients with KMLC (NCI identifier NCT03808558). We anticipate that these studies will contribute to a better understanding of cellular metabolic networks required for KM driven tumorigenesis, providing the framework for the development of novel cancer therapies.

概括肺癌（LC）是美国乃至全世界癌症相关死亡的主要原因。激活原癌基因 KRAS 突变（突变型 KRAS，此后为 KM）发生在约 30% 的非小细胞肺中癌症（非小细胞肺癌）。这些癌症与侵袭性表型、治疗耐药性和较差的预后有关。结果。 KM 在呼吸道上皮中的表达足以引发肺部肿瘤发生。此外，KM对于维持已形成的肿瘤是必需的。这些观察结果将 KM 确立为高度优先的药物靶点。只有少数 KM 驱动的 LC 患者从治疗中受益，包括免疫疗法或 KRASG12C 抑制剂。因此，KMLC 患者的预后较差。因此， KMLC 迫切需要有效的治疗方法。癌细胞经历癌基因引导的代谢重编程，以满足能量和能量的需求。细胞存活、生长和增殖的生物合成挑战。有人提议这些改变是对于维持已确定的癌症至关重要。事实上，我们发现转基因的 LC 中 KM 消失了。小鼠的饮食会导致多种代谢网络的扰动，包括脂肪酸 (FA) 的合成。为了确定脂质代谢对 KM 驱动的 LC 的贡献，我们对 KMLC 的脂质组进行了表征具有高分辨率质谱、基质辅助激光解吸/电离成像 MS (MALDI-IMS) 和功能实验。我们的初步数据表明 KM 上调脂肪酸合酶 (FASN) 合成 FA 来修复被活性氧 (ROS) 损坏的过氧化磷脂 (PL)。 FASN 在癌症中经常上调，但其作用仍然难以捉摸。我们发现抑制 FASN 与 TVB-3664 是同类首个 FASN 抑制剂 (FASNi)，可诱导铁死亡（铁和 ROS- 的一种形式）依赖性程序性细胞死亡，其特征是脂质过氧化物在体外和体内的积累 KMLC 的临床前模型。抑制 ACSL3、LPCAT3 和 LPCAT3 的脂质组学分析和功能实验 PLA2G4C 强烈建议，在 KMLC 中，FA 通过供给土地循环来发挥促生存功能，土地循环是主要的重塑 PL 过氧化酰基链的过程，使铁死亡偏转。这些观察结果支持这样的假设：KMLC 依赖 FA 来避免铁死亡并促进肿瘤发生。我们建议通过采用知识管理的多方面方法来检验这一假设转基因小鼠、LC 细胞系组、功能和脂质组学实验。值得注意的是，我们的小组提供了 TVB-2640（一种 FASNi 衍生物）在患有以下疾病的患者中进行 II 期临床试验的基本原理： KMLC（NCI 标识符 NCT03808558）。我们预计这些研究将有助于更好地理解 KM 驱动的肿瘤发生所需的细胞代谢网络，为开发提供框架新的癌症疗法。