Emerging nanomedicine strategies for hepatocellular carcinoma therapy

Author:

Guo Chen12,Zhang Jiayu2ORCID,Cai Xiaomeng2,Dou Rui2,Tang Jiaruo2,Huang Zhengyuan2,Wang Xueting2,Guo Yan2,Chen Hanqing13ORCID,Chen Jun2ORCID

Affiliation:

1. Department of Gastroenterology and Hepatology, Center for Medical Research on Innovation and Translation, The Second Affiliated Hospital, School of Medicine South China University of Technology Guangzhou China

2. CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety, Multi‐disciplinary Research Division Institute of High Energy Physics and University of Chinese Academy of Sciences (UCAS), Chinese Academy of Sciences (CAS) Beijing China

3. Department of Nutrition & Food Hygiene, School of Public Health Capital Medical University Beijing China

Abstract

AbstractHepatocellular carcinoma (HCC) is a prevalent malignant tumor with a range of risk factors, including viral infections, alcoholic liver disease, exposure to fungal toxins, obesity, and type 2 diabetes. Despite advancements in early detection and treatment, HCC continues to exhibit a high rate of recurrence. Patients in advanced stages have a poor prognosis, and the survival rate after cancer metastasis is notably low. Consequently, there exists an urgent necessity for novel treatment strategies. Nanomedicine possesses superior attributes, such as targeted administration and responsive drug release within the tumor microenvironment. These systems demonstrate potential in HCC treatment by facilitating the transportation of diverse therapeutic drugs. This comprehensive review aims to delve into the application of nanoparticle drug delivery systems in the management of liver tumors, with particular emphasis on formulation, targeted strategies specific to liver tumors, and various methods of drug release. By offering insights into the utilization of nanoparticle drug delivery systems in the realm of liver tumor treatment, this review endeavors to assist readers in exploring their vast potential.

Publisher

Wiley

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