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使用新型烟酰胺磷酸核糖转移酶(NAMPT)抑制剂OT-82靶向FH缺陷型遗传性平滑肌瘤病和肾细胞癌中的NAD+代谢脆弱性。

Targeting NAD+ Metabolism Vulnerability in FH-Deficient Hereditary Leiomyomatosis and Renal Cell Carcinoma with the Novel NAMPT Inhibitor OT-82.

作者信息

Najera Susana S, Ricketts Christopher J, Schmidt Laura S, Medina Julia I, Saito Keita, Ileva Lilia, Brender Jeffrey R, James Amy M, Peer Cody J, Gouker Brad, Karim Baktiar O, Chernova Olga, Wells Catherine, Wei Ming-Hui, Yang Youfeng, Zhang Xiaohu, Klumpp-Thomas Carleen, Travers Jameson, Chen Lu, Wilson Kelli M, Issaq Sameer H, Figg William D, Difilippantonio Simone, Kalen Joseph D, Krishna Murali C, Thomas Craig J, Ceribelli Michele, Heske Christine M, Crooks Daniel R, Meier Jordan L

机构信息

Urologic Oncology Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.

Chemical Biology Laboratory, National Cancer Institute, Frederick, Maryland.

出版信息

Mol Cancer Ther. 2025 Feb 4;24(2):200-213. doi: 10.1158/1535-7163.MCT-24-0225.

Abstract

Hereditary leiomyomatosis and renal cell cancer (HLRCC) is an inherited cancer syndrome caused by germline pathogenic variants in the fumarate hydratase (FH) gene. Affected individuals are at risk for developing cutaneous and uterine leiomyomas and aggressive FH-deficient renal cell carcinoma (RCC) with a papillary histology. Due to a disrupted tricarboxylic acid cycle, FH-deficient kidney cancers rely on aerobic glycolysis for energy production, potentially creating compensatory metabolic vulnerabilities. This study conducted a high-throughput drug screen in HLRCC cell lines, which identified a critical dependency on nicotinamide adenine dinucleotide (NAD), a redox cofactor produced by the biosynthetic enzyme nicotinamide phosphoribosyltransferase (NAMPT). Human HLRCC tumors and HLRCC-derived cell lines exhibited elevated NAMPT expression compared with controls. FH-deficient HLRCC cells, but not FH-restored HLRCC or normal kidney cells, were sensitive to NAMPT inhibition. HLRCC cell line viability was significantly decreased in both 2D and 3D in vitro cultures in response to the clinically relevant NAMPT inhibitor OT-82. NAMPT inhibition in vitro significantly decreased the total amount of NAD+, NADH, NADP, NADPH, and poly-ADP-ribose levels, and the effects of NAMPT inhibition could be rescued by the downstream NAD precursor nicotinamide mononucleotide (NMN), confirming the on-target activity of OT-82. Moreover, NAMPT inhibition by OT-82 in two HLRCC xenograft models resulted in severely reduced tumor growth. OT-82 treatment of HLRCC xenograft tumors in vivo inhibited glycolytic flux as demonstrated by reduced lactate/pyruvate ratio in hyperpolarized 13C-pyruvate magnetic resonance spectroscopic imaging experiments. Overall, our data define NAMPT inhibition as a potential therapeutic approach for FH-deficient HLRCC-associated RCC.

摘要

遗传性平滑肌瘤病和肾细胞癌(HLRCC)是一种遗传性癌症综合征,由延胡索酸水合酶(FH)基因的种系致病性变异引起。受影响的个体有发生皮肤和子宫平滑肌瘤以及具有乳头状组织学特征的侵袭性FH缺陷型肾细胞癌(RCC)的风险。由于三羧酸循环中断,FH缺陷型肾癌依靠有氧糖酵解产生能量,这可能会产生代偿性代谢脆弱性。本研究在HLRCC细胞系中进行了高通量药物筛选,确定了对烟酰胺腺嘌呤二核苷酸(NAD)的关键依赖性,NAD是由生物合成酶烟酰胺磷酸核糖基转移酶(NAMPT)产生的一种氧化还原辅助因子。与对照组相比,人类HLRCC肿瘤和HLRCC衍生的细胞系显示出NAMPT表达升高。FH缺陷型HLRCC细胞,而非FH恢复型HLRCC细胞或正常肾细胞,对NAMPT抑制敏感。在二维和三维体外培养中,临床相关的NAMPT抑制剂OT-82可显著降低HLRCC细胞系的活力。体外NAMPT抑制显著降低了NAD+、NADH、NADP、NADPH和多聚ADP-核糖水平,并且NAMPT抑制的作用可被下游NAD前体烟酰胺单核苷酸(NMN)挽救,证实了OT-82的靶向活性。此外,OT-82在两种HLRCC异种移植模型中抑制NAMPT导致肿瘤生长严重减缓。在超极化13C-丙酮酸磁共振波谱成像实验中,OT-82对HLRCC异种移植肿瘤的体内治疗抑制了糖酵解通量,表现为乳酸/丙酮酸比值降低。总体而言,我们的数据将NAMPT抑制定义为FH缺陷型HLRCC相关RCC的一种潜在治疗方法。

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