Tehran University of Medical Sciences

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):
Share this content! On (X network) By
Cost-Reduction Strategy to Culture Patient Derived Bladder Tumor Organoids Publisher Pubmed



Sisakht MM1, 2 ; Gholizadeh F2 ; Hekmatirad S2 ; Mahmoudi T3 ; Montazeri S4 ; Sharifi L4 ; Daemi H5 ; Romal S3 ; Yazdi MH1 ; Faramarzi MA1 ; Shahverdi AR1, 6 ; Hamidieh AA1, 7
Authors
Show Affiliations
Authors Affiliations
  1. 1. Biotechnology Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Stem Cell and Regenerative Medicine innovation center, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Department of Urology, Erasmus MC Cancer Institute, Erasmus University Medical Center Rotterdam, Rotterdam, Netherlands
  4. 4. Uro-oncology Research Center, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Department of Cell Engineering, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran
  6. 6. Recombinant Vaccine Research Center, Tehran University of Medical Sciences, Tehran, Iran
  7. 7. Pediatric Cell and Gene Therapy Research Center, Gene, Cell & Tissue Research Institute, Tehran University of Medical Sciences, Tehran, Iran

Source: Scientific Reports Published:2025


Abstract

Organoids as self-organized structure derived from stem cells can recapitulate the function of an organ in miniature form which have developed great potential for clinical translation, drug screening and personalized medicine. Nevertheless, the majority of patient-derived organoids (PDOs) are currently being cultured in the basement membrane matrices (BMMs), which are constrained by xenogeneic origin, batch-to-batch variability, cost, and complexity. Besides, organoid culture relies on biochemical signals provided by various growth factors in the composition of medium. We propose sodium alginate hydrogel scaffold in addition to the fibroblast conditioned medium (FCM)-enriched culture medium that is inexpensive and easily amenable to clinical applications for the culture of bladder cancer PDOs. PDOs grown in sodium alginate and FCM based medium have proliferation potential, growth rate, and gene expression that are similar to PDOs cultured in BME. According to the results, sodium alginate has substantial mechanical properties and reduces variance in early passage bladder tumor organoid cultures collected from patients. Furthermore, using FCM based medium as an alternative solution to eliminate some essential growth factors can be considered, especially for low-resource situation and develop cost effective tumor organoids. © The Author(s) 2025.