Anti-Cancer Drug Validation: the Contribution of Tissue Engineered Models

Mariana R Carvalho1,2, Daniela Lima1,2, Rui L Reis3,4

  • 13B's Research Group - Biomaterials, Biodegradables and Biomimetics, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, University of Minho, AvePark, 4806-909 Taipas, Guimarães, Portugal.

Insights

Bioengineered 3D tumor models offer a promising alternative to traditional 2D cell cultures and animal studies for drug development. These advanced models improve drug safety and efficacy testing, overcoming limitations of current methods.

Area of Science:

  • Biomedical Engineering
  • Oncology
  • Drug Discovery

Background:

  • Traditional drug development faces challenges with late-stage toxicity detection.
  • 2D cell cultures and animal models have inherent limitations in predicting human drug responses.
  • There is a critical need for more predictive preclinical models in drug screening.

Purpose of the Study:

  • To review the current state of 3D tissue models for drug discovery.
  • To explore 3D models as alternatives to traditional methods for cancer drug testing.
  • To focus on 3D models developed for nine cancer types represented by the NCI60 cell line panel.

Main Methods:

  • Literature review of "state of the art" 3D tissue models.
  • Analysis of models developed for leukemia, lung, colorectal, CNS, melanoma, ovarian, renal, prostate, and breast cancers.
  • Focus on models incorporating tissue context for drug safety and efficacy studies.

Main Results:

  • 3D bioengineered tumor models are emerging as a new generation of predictive tools.
  • These models offer potential to transform drug screening by including tissue context.
  • The review addresses specific 3D models developed for the NCI60 cancer types.

Conclusions:

  • 3D tissue models represent a significant advancement in preclinical drug development.
  • They provide a more accurate platform for evaluating drug safety and efficacy compared to traditional methods.
  • Further development and application of these models can accelerate the discovery of effective cancer therapies.