摘要4224:SGLT2是早期肺腺癌的诊断靶点

B. Villegas, E. Koziolek, Jie Liu, W. Wallace, D. Elashoff, D. Aberle, D. Shackelford, J. Barrio, J. Yanagawa, S. Dubinett, C. Scafoglio
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引用次数: 0

摘要

肺癌是癌症相关死亡的主要原因,而肺腺癌(LUAD)是最常见的组织学。早期诊断和治疗至关重要;然而,尚无针对早期LUAD的针对性诊断和治疗方法。癌症的一个重要标志是通过GLUT转运体增加葡萄糖摄取。GLUT的活性通过正电子发射断层扫描(PET)与2-[18F]氟脱氧葡萄糖(FDG)成像。FDG PET是晚期肺癌分期的标准工具,但对早期LUAD的敏感性较低。这被认为是生长缓慢和葡萄糖需求低的结果。然而,我们发现了FDG PET未检测到的一种新的代谢供应系统:葡萄糖钠转运蛋白2 (SGLT2)1。SGLT2活性可以用PET示踪剂甲基-4-[18F]氟脱氧葡萄糖(Me4FDG)在体内测量。我们发现SGLT2在人肺恶性前病变和早期LUAD中高表达。Me4FDG检测小鼠模型中fdg阴性的早期LUAD。在遗传和患者源性小鼠模型中,用fda批准的抑制剂靶向SGLT2可显著降低肿瘤生长并延长生存期,证实了SGLT2在早期LUAD2中的重要作用。早期LUAD依赖于SGLT2开启了令人兴奋的诊断和治疗机会。国家肺部筛查试验显示,使用低剂量螺旋计算机断层扫描(CT)可使高危人群的肺癌死亡率降低20%。CT对肺结节的检测非常敏感,但特异性较低,尤其是LUAD。在CT上,LUAD可表现为实性或亚实性结节。大多数亚实性结节不是癌症,许多结节会保持稳定或消退;然而,实下病变可代表癌前病变或原位腺癌。LUAD早期的这些病变在转变为侵袭性疾病之前可能持续数月至数年。因此,目前的护理标准是对这些患者进行CT成像,以监测这些不确定病变的恶性进展的放射学迹象。鉴定新的生物标志物,以预测这些结节的恶性潜能,在他们的初步鉴定是至关重要的。1Scafoglio等。中国科学(自然科学版),2015;112(30):E4111-4119。科学。Transl。引用格式:Brendon Villegas, Eva Koziolek,刘杰,W. Dean Wallace, David Elashoff, Denise R. Aberle, David B. Shackelford, Jorge R. Barrio, Jane Yanagawa, Steven M. Dubinett, Claudio Scafoglio。SGLT2是早期肺腺癌的诊断靶点[摘要]。摘自:2019年美国癌症研究协会年会论文集;2019年3月29日至4月3日;亚特兰大,乔治亚州。费城(PA): AACR;癌症杂志,2019;79(13增刊):摘要nr 4224。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract 4224: SGLT2 is a diagnostic target for early stage lung adenocarcinoma
Lung cancer is the leading cause of cancer-related death, and lung adenocarcinoma (LUAD) is the most frequent histology. Early diagnosis and treatment are essential; however, there are no targeted diagnostic and therapeutic approaches for early LUAD. An important hallmark of cancer is the increased glucose uptake via GLUT transporters. GLUT activity is imaged in cancer by positron emission tomography (PET) with 2-[18F] fluorodeoxyglucose (FDG). FDG PET is a standard tool for staging advanced lung cancer, but has low sensitivity for early-stage LUAD. This is considered a consequence of slow growth and low requirement of glucose. However, we discovered a novel system of metabolic supply not detected by FDG PET: the sodium glucose transporter 2 (SGLT2)1. SGLT2 activity can be measured in vivo with the PET tracer methyl-4-[18F] fluorodeoxyglucose (Me4FDG). We identified high expression of SGLT2 in human lung premalignancy and early-stage LUAD. Me4FDG detects early-stage, FDG-negative LUAD in mouse models. Targeting SGLT2 with FDA-approved inhibitors significantly reduces tumor growth and prolongs survival in genetic and patient-derived murine models, confirming an important role of SGLT2 in early-stage LUAD2. The reliance of early stage LUAD on SGLT2 opens exciting diagnostic and therapeutic opportunities. The National Lung Screening Trial showed a 20% reduction in lung cancer mortality in high risk individuals using low-dose helical computed tomography (CT). CT is highly sensitive for detecting lung nodules, but is limited by low specificity, especially for LUAD. On CT, LUAD may appear as solid or subsolid nodules. Most subsolid nodules are not cancer, and many will remain stable or resolve; however, subsolid lesions can represent premalignant lesions or adenocarcinoma in situ. These lesions in the early spectrum of LUAD may persist for months to years before transforming into invasive disease. As a result, current standard of care is to follow these patients with CT imaging to monitor these indeterminate lesions for radiologic signs of malignant progression. The identification of novel biomarkers to predict the malignant potential of these nodules at their initial identification is of paramount importance. 1Scafoglio et al. Proc Natl Acad Sci U S A 2015;112(30):E4111-4119 2Scafoglio et al. Sci. Transl. Med. 10, eaat5933 (2018) Citation Format: Brendon Villegas, Eva Koziolek, Jie Liu, W. Dean Wallace, David Elashoff, Denise R. Aberle, David B. Shackelford, Jorge R. Barrio, Jane Yanagawa, Steven M. Dubinett, Claudio Scafoglio. SGLT2 is a diagnostic target for early stage lung adenocarcinoma [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2019; 2019 Mar 29-Apr 3; Atlanta, GA. Philadelphia (PA): AACR; Cancer Res 2019;79(13 Suppl):Abstract nr 4224.
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