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Therapeutic targeting of a novel 6-substituted pyrrolo [2,3-d]pyrimidine thienoyl antifolate to human solid tumors based on selective uptake by the proton-coupled folate transporter.基于质子偶联叶酸转运体的选择性摄取,新型 6-取代吡咯并[2,3-d]嘧啶噻吩酰类抗叶酸药物对人实体瘤的治疗靶向作用。
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J Med Chem. 2011 Oct 27;54(20):7150-64. doi: 10.1021/jm200739e. Epub 2011 Sep 22.
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Annu Rev Nutr. 2011 Aug 21;31:177-201. doi: 10.1146/annurev-nutr-072610-145133.
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Hypermethylation of the human proton-coupled folate transporter (SLC46A1) minimal transcriptional regulatory region in an antifolate-resistant HeLa cell line.叶酸载体蛋白(SLC46A1)最小转录调控区在氨甲喋呤耐药的 HeLa 细胞系中的高甲基化。
Mol Cancer Ther. 2009 Aug;8(8):2424-31. doi: 10.1158/1535-7163.MCT-08-0938. Epub 2009 Aug 11.
8
Role of the glutamate 185 residue in proton translocation mediated by the proton-coupled folate transporter SLC46A1.谷氨酸185残基在质子偶联叶酸转运体SLC46A1介导的质子转运中的作用。
Am J Physiol Cell Physiol. 2009 Jul;297(1):C66-74. doi: 10.1152/ajpcell.00096.2009. Epub 2009 Apr 29.
9
The functional roles of the His247 and His281 residues in folate and proton translocation mediated by the human proton-coupled folate transporter SLC46A1.人类质子偶联叶酸转运体SLC46A1介导的叶酸和质子转运过程中His247和His281残基的功能作用。
J Biol Chem. 2009 Jun 26;284(26):17846-57. doi: 10.1074/jbc.M109.008060. Epub 2009 Apr 23.
10
Membrane transporters and folate homeostasis: intestinal absorption and transport into systemic compartments and tissues.膜转运蛋白与叶酸稳态:肠道吸收以及向全身各腔室和组织的转运
Expert Rev Mol Med. 2009 Jan 28;11:e4. doi: 10.1017/S1462399409000969.

碳酸根离子和其他阴离子对质子偶联叶酸转运蛋白(PCFT-SLC46A1)的抑制作用。

Inhibition of the proton-coupled folate transporter (PCFT-SLC46A1) by bicarbonate and other anions.

机构信息

Department of Molecular Pharmacology, Albert Einstein College of Medicine, Chanin 628, 1300 Morris Park Avenue, Bronx, NY 10461, USA.

出版信息

Mol Pharmacol. 2013 Jul;84(1):95-103. doi: 10.1124/mol.113.085605. Epub 2013 Apr 22.

DOI:10.1124/mol.113.085605
PMID:23609145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3684825/
Abstract

The proton-coupled folate transporter (PCFT) plays a key role in intestinal folate absorption, and loss-of-function mutations in the gene encoding this transporter are the molecular basis for hereditary folate malabsorption. Using a stable transfectant with high expression of PCFT, physiologic levels of bicarbonate produced potent and rapidly reversible inhibition of PCFT-mediated transport at neutral pH. Bisulfite and nitrite also inhibited PCFT function at neutral pH, whereas sulfate, nitrate, and phosphate had no impact at all. At weakly acidic pH (6.5), bisulfite and nitrite exhibited much stronger inhibition of PCFT-mediated transport, whereas sulfate and nitrate remained noninhibitory. Inhibition by bisulfite and nitrite at pH 6.5 was associated with a marked decrease in the influx Vmax and collapse of the transmembrane proton gradient attributed to the diffusion of the protonated forms into these cells. Monocarboxylates such as pyruvate and acetate also collapsed the pH gradient and were also inhibitory, whereas citrate and glycine neither altered the proton gradient nor inhibited PCFT-mediated transport. These observations add another dimension to the unfavorable pH environment for PCFT function in systemic tissues: the presence of high concentrations of bicarbonate.

摘要

质子偶联叶酸转运蛋白(PCFT)在肠道叶酸吸收中发挥关键作用,该转运蛋白基因的功能丧失突变是遗传性叶酸吸收不良的分子基础。使用高表达 PCFT 的稳定转染细胞系,生理浓度的碳酸氢盐在中性 pH 下对 PCFT 介导的转运产生强大且快速可逆的抑制作用。亚硫酸氢盐和亚硝酸盐在中性 pH 下也抑制 PCFT 功能,而硫酸盐、硝酸盐和磷酸盐则完全没有影响。在弱酸性 pH(6.5)下,亚硫酸氢盐和亚硝酸盐对 PCFT 介导的转运的抑制作用更强,而硫酸盐和硝酸盐仍然没有抑制作用。亚硫酸氢盐和亚硝酸盐在 pH 6.5 时的抑制作用与内流 Vmax 的显著下降以及跨膜质子梯度的崩溃有关,这归因于质子化形式扩散到这些细胞中。单羧酸如丙酮酸和醋酸盐也会使 pH 梯度崩溃并具有抑制作用,而柠檬酸和甘氨酸既不改变质子梯度也不抑制 PCFT 介导的转运。这些观察结果为 PCFT 在全身组织中的功能增加了另一个不利 pH 环境:高浓度的碳酸氢盐。