Combined Hyaluronic Acid Nanobioconjugates Impair CD44-Signaling for Effective Treatment Against Obesity: A Review of Comparison with Other Actors.

IF 6.5 2区 医学 Q1 NANOSCIENCE & NANOTECHNOLOGY
International Journal of Nanomedicine Pub Date : 2025-08-21 eCollection Date: 2025-01-01 DOI:10.2147/IJN.S529250
Daniel Ejim Uti, Wilson Achu Omang, Esther Ugo Alum, Okechukwu Paul-Chima Ugwu, Margaret Amieibi Wokoma, Rowland Inalegwu Oplekwu, Item Justin Atangwho, Godwin Eneji Egbung
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Abstract

CD44, a key hyaluronic acid (HA) receptor, has emerged as a central mediator of adipose tissue inflammation, remodeling, and insulin resistance in obesity. Its overexpression in obese adipose depots promotes leukocyte infiltration, pro-inflammatory signaling, and extracellular matrix dysregulation processes that underlie metabolic dysfunction. This review explores the therapeutic relevance of targeting the HA-CD44 axis by synthesizing data primarily from preclinical studies, with emerging evidence from early clinical investigations. A narrative review methodology was employed to assess and compare therapeutic modalities, highlighting advances in molecular targeting, drug delivery systems, and metabolic interventions. We focus on two primary therapeutic classes: small molecules and nanobioconjugates. Small molecules, such as curcumin, metformin, and CD44 antagonists, offer systemic modulation and accessibility but are limited by their low tissue specificity and potential side effects. In contrast, HA-functionalized nanobioconjugates, including liposomes, PLGA nanoparticles, dendrimers, and exosomes, enable targeted delivery to adipose tissue, prolonged drug release, and reduced systemic toxicity. These nanosystems have demonstrated superior modulation of CD44 signaling, adipose inflammation, and glucose homeostasis in obesity models. Emerging strategies such as monoclonal antibodies, GLP-1 analogs, gene-editing tools (eg, CRISPR/Cas9), microbiome modulators, and brown adipose tissue (BAT) activators are also discussed. A comparative analysis indicates that nanobioconjugates offer the highest targeting precision, while small molecules remain advantageous in terms of cost and ease of administration. However, biologics and gene therapies face challenges related to delivery and scalability. Collectively, current evidence predominantly preclinical supports the HA-CD44 axis as a promising therapeutic target in obesity. Integrated approaches combining nanotechnology with molecular inhibitors and biologics could offer a multifaceted strategy for managing metabolic disease.

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复合透明质酸纳米生物偶联物损害cd44信号通路以有效治疗肥胖:与其他参与者的比较综述
CD44是一种关键的透明质酸(HA)受体,是肥胖症中脂肪组织炎症、重塑和胰岛素抵抗的中心介质。它在肥胖脂肪库中的过度表达促进了白细胞浸润、促炎信号和细胞外基质失调过程,这些过程是代谢功能障碍的基础。本文通过综合临床前研究数据和早期临床研究的新证据,探讨了靶向HA-CD44轴的治疗相关性。采用叙述性回顾方法来评估和比较治疗方式,强调分子靶向,药物传递系统和代谢干预方面的进展。我们专注于两个主要的治疗类:小分子和纳米生物偶联物。小分子,如姜黄素、二甲双胍和CD44拮抗剂,提供全身调节和可及性,但受其低组织特异性和潜在副作用的限制。相比之下,ha功能化的纳米生物偶联物,包括脂质体、PLGA纳米颗粒、树状大分子和外泌体,能够靶向递送到脂肪组织,延长药物释放时间,降低全身毒性。在肥胖模型中,这些纳米系统已经证明了对CD44信号、脂肪炎症和葡萄糖稳态的优越调节。新兴策略,如单克隆抗体,GLP-1类似物,基因编辑工具(如CRISPR/Cas9),微生物组调节剂和棕色脂肪组织(BAT)激活剂也进行了讨论。一项比较分析表明,纳米生物偶联物提供了最高的靶向精度,而小分子在成本和易于管理方面仍然具有优势。然而,生物制剂和基因疗法面临着递送和可扩展性方面的挑战。总的来说,目前的临床前证据主要支持HA-CD44轴作为肥胖的有希望的治疗靶点。将纳米技术与分子抑制剂和生物制剂相结合的综合方法可以为管理代谢性疾病提供多方面的策略。
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来源期刊
International Journal of Nanomedicine
International Journal of Nanomedicine NANOSCIENCE & NANOTECHNOLOGY-PHARMACOLOGY & PHARMACY
CiteScore
14.40
自引率
3.80%
发文量
511
审稿时长
1.4 months
期刊介绍: The International Journal of Nanomedicine is a globally recognized journal that focuses on the applications of nanotechnology in the biomedical field. It is a peer-reviewed and open-access publication that covers diverse aspects of this rapidly evolving research area. With its strong emphasis on the clinical potential of nanoparticles in disease diagnostics, prevention, and treatment, the journal aims to showcase cutting-edge research and development in the field. Starting from now, the International Journal of Nanomedicine will not accept meta-analyses for publication.
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