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ME3BP-7是一种靶向细胞毒性药物,可迅速杀死表达高水平单羧酸转运蛋白MCT1的胰腺癌细胞。

ME3BP-7 is a targeted cytotoxic agent that rapidly kills pancreatic cancer cells expressing high levels of monocarboxylate transporter MCT1.

作者信息

Rincon-Torroella Jordina, Dal Molin Marco, Mog Brian, Han Gyuri, Watson Evangeline, Wyhs Nicolas, Ishiyama Shun, Ahmedna Taha, Minn Il, Azad Nilofer, Bettegowda Chetan, Papadopoulos Nickolas, Kinzler Kenneth W, Zhou Shibin, Vogelstein Bert, Gabrielson Kathleen, Sur Surojit

机构信息

Ludwig Center, Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins University School of Medicine, Baltimore, United States.

Department of Neurosurgery, The Johns Hopkins University School of Medicine, Baltimore, United States.

出版信息

Elife. 2025 May 20;13:RP94488. doi: 10.7554/eLife.94488.

Abstract

Nearly 30% of pancreatic ductal adenocarcinomas (PDACs) exhibit a marked overexpression of monocarboxylate transporter 1 (MCT1) offering a unique opportunity for therapy. However, biochemical inhibitors of MCT1 have proven unsuccessful in clinical trials. In this study, we present an alternative approach using 3-bromopyruvate (3BP) to target MCT1 overexpressing PDACs. 3BP is a cytotoxic agent that is known to be transported into cells via MCT1, but its clinical usefulness has been hampered by difficulties in delivering the drug systemically. We describe here a novel microencapsulated formulation of 3BP (ME3BP-7), which is effective against a variety of PDAC cells in vitro and remains stable in serum. Furthermore, systemically administered ME3BP-7 significantly reduces pancreatic cancer growth and metastatic spread in multiple orthotopic models of pancreatic cancer with manageable toxicity. ME3BP-7 is, therefore, a prototype of a promising new drug, in which the targeting moiety and the cytotoxic moiety are both contained within the same single small molecule.

摘要

近30%的胰腺导管腺癌(PDAC)表现出单羧酸转运蛋白1(MCT1)的显著过表达,这为治疗提供了独特的机会。然而,MCT1的生化抑制剂在临床试验中已被证明是不成功的。在本研究中,我们提出了一种使用3-溴丙酮酸(3BP)靶向MCT1过表达的PDAC的替代方法。3BP是一种细胞毒性剂,已知可通过MCT1转运到细胞中,但其临床应用因药物全身递送困难而受到阻碍。我们在此描述了一种新型的3BP微囊化制剂(ME3BP-7),它在体外对多种PDAC细胞有效,并且在血清中保持稳定。此外,全身给药的ME3BP-7在多种胰腺癌原位模型中显著降低胰腺癌的生长和转移扩散,且毒性可控。因此,ME3BP-7是一种有前景的新药的原型,其中靶向部分和细胞毒性部分都包含在同一个小分子中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70d1/12092006/d613b1e69a85/elife-94488-fig1.jpg

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