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Anti-Inflammatory Effect of Mesenchymal Stem Cells on Hepatocellular Carcinoma in the Xenograft Mice Model Publisher Pubmed



Hajighasemlou S1, 2 ; Nikbakht M3 ; Pakzad S2 ; Azadbakht A4, 5 ; Muhammadnejad S6 ; Mirmoghtadaei M7, 8 ; Gharibzadeh S9 ; Seyhoun I1 ; Verdi J1
Authors
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Authors Affiliations
  1. 1. Department of Tissue Engineering & Applied Cell Sciences, Tehran University of Medical Sciences (TUMS), Tehran, Iran
  2. 2. Food and Drug Administration, Ministry of Health and Medical Education, Tehran, Iran
  3. 3. Hematology, Oncology & Stem Cell Transplantation Research Center, Tehran University of Medical Sciences (TUMS), Tehran, Iran
  4. 4. Department of Biomedical Engineering, Central Tehran Branch, Islamic Azad university, Tehran, Iran
  5. 5. Stem cells Research Center, Tissue Engineering and Regenerative Medicine Institute, Central Tehran Branch, Islamic Azad university, Tehran, Iran
  6. 6. Gene Therapy Research Center, Digestive Diseases Research Institute, Tehran University of Medical Sciences, Tehran, Iran
  7. 7. Immunology, Asthma and Allergy Research Institute, Tehran University of Medical Sciences (TUMS), Tehran, Iran
  8. 8. Children's Medical Center, Pediatrics Center of Excellence, Tehran University of Medical Sciences (TUMS), Tehran, Iran
  9. 9. Department of Epidemiology and Biostatistics Research Centre for Emerging and Reemerging Infectious Diseases, Pasteur institute, Tehran, Iran

Source: Veterinary Medicine and Science Published:2022


Abstract

Background: Hepatocellular carcinoma (HCC) is the fifth most diagnosed cancer and the second leading cause of cancer-related deaths worldwide. Sorafenib is the standard treatment used in the advanced stages of HCC. Cell therapy with mesenchymal stem cells (MSCs)-based cell therapy has proven effective in immune regulation and tumour growth inhibition. Objectives: In this study, we investigated the anti-inflammatory effect of MSCs on HCC xenografts. Methods: Human HepG2 cell lines were subcutaneously implanted into the flank of 12 nude mice, divided into three groups: the control group, the IV group (intravenous MSCs injection) and the local group (local MSCs injection). Mice were sacrificed 6 weeks after tumour implantation, and tumours were resected entirety. Quantitative real-time polymerase chain reaction (qRT-PCR) measured the gene expression of inflammatory markers, including tumour necrosis factor-α (TNF-α), interleukin (IL)-1α and IL-10. Aspartate transaminase (AST), alanine transaminase (ALT) and urea levels were measured using spectrophotometry to ensure the safety of MSC therapy. Results: Gene expressions for all three inflammatory markers were reduced in both MSCs groups compared to the control group. AST, ALT and urea levels remained in normal ranges. Conclusions: MSC therapy can reduce inflammation in HCC xenograft mouse models. © 2022 The Authors. Veterinary Medicine and Science published by John Wiley & Sons Ltd.