人体有机阳离子转运体的使用和药物靶标反应

Badiginchala Navya Sai, Hindustan Abdul Ahad, Haranath Chinthaginjala, Bake Meharajunnisa, Siriguppa Dheeraj, Mallem Venkata Barath
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引用次数: 0

摘要

本研究旨在探讨人体有机阳离子摄取转运体及其在生物运输中的关键功能。hOCT在肝脏中广泛表达,并被发现具有广泛的底物选择性,这是由SLC22A1基因编码的。OCT1促进分子扩散,使营养物质进入细胞。根据最近的研究,OCT1可以帮助吸收用于治疗癌症等疾病的药物。功能受损的OCT1,其外观水平与对多种药物的反应有关,是耐药性的根本原因。最近,在药物基因组学研究中,一个重要的药理靶点被提出为OCT1。整个OCT1基因包含一些单核苷酸多态性。同样未知的是OCT1识别一系列配体所需的特定变化或与其他蛋白质的相互作用。作者在这篇综述中提出了最新的OCT1发现,以刺激对这一重要摄取转运体的进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Human Organic Cation Transporter Use and Drug Target Responses
The goal of the current work was to explore the human organic cation uptake transporter and its critical function in biological transportation. The hOCT is extensively articulated in the liver and has been found to have a broad range of substrate selectivity, which is encoded by the SLC22A1 gene. OCT1 promotes molecular diffusion, enabling nutrients to enter the cell. OCT1 can aid in the absorption of drugs used to treat illnesses like cancer, according to recent research. Functionally impaired OCT1, whose appearance levels are associated with responses to a variety of medications, is the root cause of drug resistance. One of the important pharmacological targets employed in pharmacogenomic studies has recently been proposed as OCT1. The entire OCT1 gene contains a few single nucleotide polymorphisms. Also unknown are the specific changes or interactions with other proteins required for OCT1 to recognize a range of ligands. The authors presented the most recent OCT1 findings in this review to stimulate further investigation into this crucial uptake transporter.
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