Terasaki Institute scientists developed a 3D model replicating chemoresistance in glioblastoma by including pericytes, a critical component of the tumor microenvironment.
The model integrates human GBM tumor cells with pericytes in a biomaterial scaffold mimicking brain tissue properties, enhancing drug response studies.
Pericyte presence led to increased temozolomide (TMZ) resistance in GBM cell lines, linked to elevated CCL5 levels, a potential therapeutic target for overcoming chemoresistance.
By emulating tissue-level properties accurately, the 3D model enables in-depth analysis of tumor-stroma interactions crucial for drug resistance mechanisms.
The model supports precision medicine by assessing individual tumor responses and facilitating high-throughput drug screening in a tumor-like environment.
This innovative platform offers a cost-effective, scalable alternative to animal models, aiding in oncology drug development and screening programs.
The biomaterial scaffold's design mimics key physical properties influencing tumor behavior, enhancing the model's ability to replicate the brain tissue's constraints.
Pericytes play a significant role in creating a protective niche for GBM cells, reducing TMZ efficacy, highlighting a potential avenue for therapeutic intervention.
The study's publication in Acta Biomaterialia marks a landmark achievement at the intersection of tissue engineering, cancer biology, and translational medicine.
The model developed by Terasaki Institute scientists holds promise in reshaping preclinical research by elucidating tumor microenvironment dynamics in drug resistance modulation.