Shafi Sadat, Khan Mohammad Ahmed, Ahmad Javed, Rabbani Syed Arman, Singh Shailja, Najmi Abul Kalam
Department of Pharmacology, School of Pharmaceutical Education and Research, Jamia Hamdard, New Delhi, 110062, India.
Special Centre for Molecular Medicine, Jawaharlal Nehru University, New Delhi, 110067, India.
Curr Drug Targets. 2025;26(2):109-131. doi: 10.2174/0113894501335877240926101134.
Metabolic reprogramming and altered cellular energetics have been recently established as an important cancer hallmark. The modulation of glucose metabolism is one of the important characteristic features of metabolic reprogramming in cancer. It contributes to oncogenic progression by supporting the increased biosynthetic and bio-energetic demands of tumor cells. This oncogenic transformation consequently results in elevated expression of glucose transporters in these cells. Moreover, various cancers exhibit abnormal transporter expression patterns compared to normal tissues. Recent investigations have underlined the significance of glucose transporters in regulating cancer cell survival, proliferation, and metastasis. Abnormal regulation of these transporters, which exhibit varying affinities for hexoses, could enable cancer cells to efficiently manage their energy supply, offering a crucial edge for proliferation. Exploiting the upregulated expression of glucose transporters, GLUTs, and Sodium Linked Glucose Transporters (SGLTs), could serve as a novel therapeutic intervention for anti-cancer drug discovery as well as provide a unique targeting approach for drug delivery to specific tumor tissues. This review aims to discussthe previous and emerging research on the expression of various types of glucose transporters in tumor tissues, the role of glucose transport inhibitors as a cancer therapy intervention as well as emerging GLUT/SGLT-mediated drug delivery strategies that can be therapeutically employed to target various cancers.
代谢重编程和细胞能量代谢改变最近已被确立为一种重要的癌症标志。葡萄糖代谢的调节是癌症代谢重编程的重要特征之一。它通过支持肿瘤细胞增加的生物合成和生物能量需求来促进致癌进展。这种致癌转化因此导致这些细胞中葡萄糖转运蛋白的表达升高。此外,与正常组织相比,各种癌症表现出异常的转运蛋白表达模式。最近的研究强调了葡萄糖转运蛋白在调节癌细胞存活、增殖和转移中的重要性。这些对己糖具有不同亲和力的转运蛋白的异常调节,可使癌细胞有效地管理其能量供应,为增殖提供关键优势。利用葡萄糖转运蛋白(GLUTs)和钠依赖性葡萄糖转运体(SGLTs)的上调表达,可作为抗癌药物发现的一种新型治疗干预手段,并为向特定肿瘤组织进行药物递送提供独特的靶向方法。本综述旨在讨论以往及新出现的关于肿瘤组织中各种类型葡萄糖转运蛋白表达的研究、葡萄糖转运抑制剂作为癌症治疗干预手段的作用,以及可用于治疗各种癌症的新出现的GLUT/SGLT介导的药物递送策略。