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希望阻断剂(DON):通过谷氨酰胺拮抗作用饿死胰腺癌。

DON of Hope: Starving Pancreatic Cancer by Glutamine Antagonism.

机构信息

Department of Pathology, New York University Grossman School of Medicine, New York, New York.

Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, New York University Grossman School of Medicine, New York, New York.

出版信息

Cancer Res. 2024 Feb 1;84(3):349-350. doi: 10.1158/0008-5472.CAN-23-3954.

Abstract

A promising approach to treat solid tumors involves disrupting their reliance on glutamine, a key component for various metabolic processes. Traditional attempts using glutamine inhibitors like 6-diazo-5-oxo-L-norleucine (DON) and CB-839 were unsuccessful, but new hope arises with DRP-104, a prodrug of DON. This compound effectively targets tumor metabolism while minimizing side effects. In a recent study published in Nature Cancer, Encarnación-Rosado and colleagues demonstrated in preclinical models that pancreatic ductal adenocarcinoma (PDAC) responds well to DRP-104, although tumors adapt through the MEK/ERK signaling pathway, which can be countered by the MEK inhibitor trametinib. In a related study, Recouvreux and colleagues found that DON is effective against pancreatic tumors, revealing that PDAC tumors upregulate asparagine synthesis in response to DON, making them susceptible to asparaginase treatment. Both studies underscore the potential of inhibiting glutamine metabolism and adaptive pathways as a promising strategy against PDAC. These findings pave the way for upcoming clinical trials utilizing DRP-104 and similar glutamine antagonists in the battle against solid tumors.

摘要

一种有前途的治疗实体瘤的方法涉及破坏它们对谷氨酰胺的依赖,谷氨酰胺是各种代谢过程的关键组成部分。使用谷氨酰胺抑制剂(如 6-重氮-5-氧-L-正亮氨酸(DON)和 CB-839)的传统尝试都没有成功,但 DRP-104 的出现带来了新的希望,DRP-104 是 DON 的前药。这种化合物可以有效地靶向肿瘤代谢,同时最大限度地减少副作用。在最近发表在《自然癌症》杂志上的一项研究中,Encarnación-Rosado 及其同事在临床前模型中表明,胰腺导管腺癌(PDAC)对 DRP-104 反应良好,尽管肿瘤通过 MEK/ERK 信号通路适应,MEK 抑制剂 trametinib 可以对抗这种信号通路。在一项相关研究中,Recouvreux 及其同事发现 DON 对胰腺肿瘤有效,这表明 PDAC 肿瘤上调天冬酰胺合成以响应 DON,使它们易受天冬酰胺酶治疗的影响。这两项研究都强调了抑制谷氨酰胺代谢和适应性途径作为对抗 PDAC 的一种有前途的策略的潜力。这些发现为即将进行的临床试验铺平了道路,这些临床试验将利用 DRP-104 和类似的谷氨酰胺拮抗剂来对抗实体瘤。

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