Yadav Dharmendra Kumar, Singh Desh Deepak, Shin Dongyun
College of Pharmacy, Gachon University Hambakmoeiro 191, Yeonsu-gu Incheon 21924 Republic of Korea
Amity Institute of Biotechnology, Amity University Rajasthan Jaipur India.
RSC Med Chem. 2024 Dec 17. doi: 10.1039/d4md00786g.
Aquaporins (AQPs) are integral membrane proteins responsible for facilitating the transmembrane transport of water and small solutes. Their involvement in diverse physiological functions extends to pathological conditions, including cancer, positioning them as promising targets for anticancer therapy. Tumor cells, particularly those with high metastatic potential, exhibit elevated AQP expression, reinforcing their critical role in tumor biology. Emerging evidence highlights AQPs' involvement in key oncogenic processes such as cell migration, proliferation, and tumor-associated edema, suggesting their potential as novel therapeutic targets. Despite this, the development of selective and potent AQP inhibitors has proven challenging. Efforts to produce small-molecule AQP inhibitors have largely been unsuccessful. However, recent advancements include monoclonal human IgG antibodies targeting extracellular domains of aquaporin-4, offering new therapeutic strategies, particularly in glioblastoma, where AQP-4 is overexpressed. However, recent advancements include monoclonal human IgG antibodies targeting extracellular domains of aquaporin-4, offering new therapeutic strategies, particularly in glioblastoma, where AQP-4 is over expressed. These antibodies hold promise for selectively targeting and eradicating AQP-4-expressing cells in malignant brain tumors. This review discusses the critical role AQPs play in cancer, including their contributions to tumor cell proliferation, migration, angiogenesis, and edema formation. Additionally, we explore innovative therapeutic approaches, such as antibody-based interventions, and outline potential future research directions in AQP-targeted cancer therapies.
水通道蛋白(AQPs)是整合膜蛋白,负责促进水和小分子溶质的跨膜运输。它们参与多种生理功能,这一作用延伸到包括癌症在内的病理状况,使它们成为抗癌治疗中有前景的靶点。肿瘤细胞,尤其是那些具有高转移潜能的肿瘤细胞,表现出水通道蛋白表达升高,这强化了它们在肿瘤生物学中的关键作用。新出现的证据突显了水通道蛋白参与细胞迁移、增殖和肿瘤相关水肿等关键致癌过程,表明它们作为新型治疗靶点的潜力。尽管如此,开发选择性强效的水通道蛋白抑制剂已被证明具有挑战性。生产小分子水通道蛋白抑制剂的努力大多未成功。然而,最近的进展包括靶向水通道蛋白4细胞外结构域的单克隆人IgG抗体,提供了新的治疗策略,特别是在水通道蛋白4过表达的胶质母细胞瘤中。这些抗体有望在恶性脑肿瘤中选择性地靶向和根除表达水通道蛋白4的细胞。本综述讨论了水通道蛋白在癌症中所起的关键作用,包括它们对肿瘤细胞增殖、迁移、血管生成和水肿形成的作用。此外,我们探索了创新的治疗方法,如基于抗体的干预措施,并概述了水通道蛋白靶向癌症治疗未来潜在的研究方向。