Az orvos-, egészségtudományi- és gyógyszerészképzés tudományos műhelyeinek fejlesztése(EFOP-3.6.3-VEKOP-16-2017-00009)
Támogató: EFOP-VEKOP
(STIA-POC-2023)
(STIA-KFI-2020)
(2024–2.1.1-EKOP-2024–00004)
(ÚNKP-23-06-SE-09)
Bolyai János Kutatási Ösztöndíj(bo_187_24) Támogató: MTA Bolyai pályázat
Three‐dimensional (3D) cell culture models derived from patient tumors are currently
under development to recapitulate in vivo physiological conditions and assess therapeutic
responses. In vitro models often fail to replicate the drug sensitivity observed in
humans. In this study, a standardized in vitro culturing method using a 3D bioprinted
breast cancer tumor model was established. We compared traditional two‐dimensional
(2D), spheroid, and 3D bioprinted in vitro models as well as in vivo growing syngeneic
or xenograft tumors. Our aim was to determine whether 3D bioprinted in vitro cultures
can represent tissue heterogeneity, growth capacity, and/or drug response as potential
tools for personalized drug sensitivity tests. Our findings demonstrated that 3D bioprinted
models closely mimic in vivo tumor morphology and drug responses, outperforming 2D
cultures and patient‐derived xenografts (PDX) in severe combined immunodeficiency
mice. Additionally, 3D bioprinted models showed similar drug sensitivity to syngeneic
tumors regrown in BALB/c mice, highlighting their potential for better therapeutic
response predictions. Our results support the use of 3D bioprinted tumor models for
personalized oncology. The presented approach could significantly advance personalized
cancer therapy by using 3D bioprinted tumor tissues, offering a more accurate representation
of tumor behavior and treatment efficacy compared to currently used PDX models.