Translational Oncology (Jul 2024)

Multifunctional and stimuli-responsive liposomes in hepatocellular carcinoma diagnosis and therapy

  • Seyedeh Setareh Samaei,
  • Mahshid Daryab,
  • Sarah Gholami,
  • Aryan Rezaee,
  • Navid Fatehi,
  • Romina Roshannia,
  • Saeed Hashemi,
  • Nazanin Javani,
  • Parham Rahmanian,
  • Reza Amani-Beni,
  • Mohammad Arad Zandieh,
  • Noushin Nabavi,
  • Mohsen Rashidi,
  • Neda Malgard,
  • Mehrdad Hashemi,
  • Afshin Taheriazam

Journal volume & issue
Vol. 45
p. 101975

Abstract

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Hepatocellular carcinoma (HCC) is the most prevalent type of liver cancer, mainly occurring in Asian countries with an increased incidence rate globally. Currently, several kinds of therapies have been deployed for HCC therapy including surgical resection, chemotherapy, radiotherapy and immunotherapy. However, this tumor is still incurable, requiring novel strategies for its treatment. The nanomedicine has provided the new insights regarding the treatment of cancer that liposomes as lipid-based nanoparticles, have been widely applied in cancer therapy due to their biocompaitiblity, high drug loading and ease of synthesis and modification. The current review evaluates the application of liposomes for the HCC therapy. The drugs and genes lack targeting ability into tumor tissues and cells. Therefore, loading drugs or genes on liposomes can increase their accumulation in tumor site for HCC suppression. Moreover, the stimuli-responsive liposomes including pH-, redox- and light-sensitive liposomes are able to deliver drug into tumor microenvironment to improve therapeutic index. Since a number of receptors upregulate on HCC cells, the functionalization of liposomes with lactoferrin and peptides can promote the targeting ability towards HCC cells. Moreover, phototherapy can be induced by liposomes through loading phtoosensitizers to stimulate photothermal- and photodynamic-driven ablation of HCC cells. Overall, the findings are in line with the fact that liposomes are promising nanocarriers for the treatment of HCC.

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