中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Nanotechnology-based shikonin delivery strategies for modulating the tumor immune microenvironment efficacy

文献类型:期刊论文

作者Kalambhe, Dipika Ramdas6,7; Asrorov, Akmal M.1,8,9; Mukhammedov, Nurkhodja2,3; Huang, Yongzhuo6,7; Wu, Aihua4; Zhao, Pengfei5
刊名DRUG DELIVERY AND TRANSLATIONAL RESEARCH
出版日期2025-08-11
页码16
关键词Nano delivery systems Shikonin PKM2 inhibition Tumor immune microenvironment
ISSN号2190-393X
DOI10.1007/s13346-025-01943-4
英文摘要Malignant tumors remain a major cause of global mortality and pose a formidable threat to human health. While natural and synthetic substances have been explored for cancer therapy, natural products such as shikonin (SHK), a naphthalene quinone extracted from Lithospermum erythrorhizon, offer unique advantages due to their plant-based origins and multifaceted pharmaceutical properties. SHK exhibits potent anticancer activity and inhibits pyruvate kinase M2 (PKM2), which suppresses glycolysis and lactate metabolism. The metabolic regulation inhibits adenosine triphosphate (ATP) production and suppresses the immunosuppressive phenotype of immune cells (e.g., Tregs), thus remodeling the tumor immune microenvironment. Additionally, SHK promotes apoptosis and anti-angiogenesis by affecting key molecular pathways, such as HIF-1 alpha, STAT3, and VEGF. However, its clinical translation is hindered by low water solubility and bioavailability, non-specific toxicity, and rapid systemic clearance. Recent advances in nanotechnology have addressed these limitations through the development of nanosized drug delivery systems, including liposomes, nanoparticles, micelles, nanogels, and other nano-formulations. These systems enhance tumor-targeted delivery, improve pharmacokinetics, and potentiate the immunomodulatory effects of SHK by reprogramming the tumor microenvironment. This review highlights the mechanisms underlying SHK antitumor immunity, evaluates the latest nanotechnology strategies to optimize SHK delivery, and discusses the challenges and prospects for translating SHK-based therapies into clinical practice.
WOS关键词REGULATORY T-CELLS ; PYRUVATE-KINASE ; LACTIC-ACID ; CANCER-CELLS ; ACTIVATION ; NANOPARTICLES ; THERAPY ; NANOMEDICINES ; DEGRADATION ; METASTASIS
资助项目Key Technologies Research and Development Program
WOS研究方向Instruments & Instrumentation ; Research & Experimental Medicine ; Pharmacology & Pharmacy
语种英语
WOS记录号WOS:001548095200001
出版者SPRINGER HEIDELBERG
源URL[http://119.78.100.183/handle/2S10ELR8/321261]  
专题国家级研究中心_原创新药研究全国重点实验室
通讯作者Wu, Aihua; Zhao, Pengfei
作者单位1.Ctr Genom & Bioinformat, 2 Univ St, Qibray 111215, Tashkent Region, Uzbekistan
2.Natl Univ Uzbekistan, Dept Nat Cpds & Appl Chem, Tashkent 100174, Uzbekistan
3.Kokand Univ, Andijan Branch, Jasorat 43, Andijan 170619, Uzbekistan
4.Zhejiang Univ, Sch Med, Sir Run Run Shaw Hosp, Dept Pharm, 3rd East Qingchun Rd, Hangzhou 310016, Zhejiang, Peoples R China
5.Zhejiang Univ, Ctr Clin Pharmacol, Affiliated Hosp 2, Sch Med, 88 Jiefang Rd, Hangzhou 310009, Peoples R China
6.Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China
7.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
8.Uzbek Acad Sci, Inst Bioorgan Chem, 83 M Ulugbek Str, Tashkent 100125, Uzbekistan
9.Alfraganus Univ, 2a Yukori Karakamish St, Tashkent 100190, Uzbekistan
推荐引用方式
GB/T 7714
Kalambhe, Dipika Ramdas,Asrorov, Akmal M.,Mukhammedov, Nurkhodja,et al. Nanotechnology-based shikonin delivery strategies for modulating the tumor immune microenvironment efficacy[J]. DRUG DELIVERY AND TRANSLATIONAL RESEARCH,2025:16.
APA Kalambhe, Dipika Ramdas,Asrorov, Akmal M.,Mukhammedov, Nurkhodja,Huang, Yongzhuo,Wu, Aihua,&Zhao, Pengfei.(2025).Nanotechnology-based shikonin delivery strategies for modulating the tumor immune microenvironment efficacy.DRUG DELIVERY AND TRANSLATIONAL RESEARCH,16.
MLA Kalambhe, Dipika Ramdas,et al."Nanotechnology-based shikonin delivery strategies for modulating the tumor immune microenvironment efficacy".DRUG DELIVERY AND TRANSLATIONAL RESEARCH (2025):16.

入库方式: OAI收割

来源:上海药物研究所

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