Mesenchymal stem cell‑derived exosomes loaded with 5‑Fu against cholangiocarcinoma .

Mol Med Rep

Department of Hepatobiliary Surgery, Taizhou People's Hospital, The Fifth Affiliated Hospital of The Medical School of Nantong University, Taizhou, Jiangsu 225300, P.R. China.

Published: June 2022

AI Article Synopsis

  • Cholangiocarcinoma (CCA) is a highly aggressive cancer that often shows no symptoms in its early stages.
  • Recent studies highlight exosomes as promising carriers for delivering chemotherapy drugs, specifically to combat tumor growth.
  • The research demonstrates that exosomes derived from human bone marrow mesenchymal stem cells can effectively deliver 5-fluorouracil (5-Fu), with the sonication method showing better loading efficiency, leading to significantly reduced viability of CCA cells compared to free 5-Fu.

Article Abstract

Cholangiocarcinoma (CCA) is an intractable malignant tumour with a high degree of malignancy that is asymptomatic in the early stages. Exosomes have been shown in numerous studies in recent years to be effective delivery vehicles for chemotherapy drugs to suppress tumour proliferation and growth and . In order to explore the inhibition of 5‑fluorouracil (5‑Fu)‑loaded exosomes on CCA growth, the present study used human bone marrow mesenchymal stem cell‑derived exosomes, as well as incubation and sonication methods for 5‑Fu loading into exosomes, to treat CCA . The findings demonstrated that exosomes isolated from mesenchymal stem cells have typical exosome characteristics. Both the incubation and sonication methods successfully loaded 5‑Fu into the exosomes (5‑Fu‑Exos), with the sonication method having a higher loading efficiency than the incubation method. When compared to the free 5‑Fu group, the 5‑Fu‑Exos group significantly inhibited the viability of CCA cells (P<0.01), indicating that 5‑Fu‑Exos can be an effective chemotherapy drug for CCA treatment.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9133964PMC
http://dx.doi.org/10.3892/mmr.2022.12729DOI Listing

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