Non-small cell lung carcinoma spheroid models in agarose microwells for drug response studies

Qiyue Luan1, Jeffrey H Becker2,3, Celine Macaraniag1

  • 1Department of Biomedical Engineering, University of Illinois Chicago, 851 S. Morgan Street, 218 SEO, Chicago, IL 60607, USA. papauts@uic.edu.

Lab on a Chip
|May 13, 2022
PubMed

Insights

A new 3D-printed platform creates uniform cancer spheroids for personalized non-small cell lung carcinoma (NSCLC) treatment testing. This 3D culture system effectively evaluates drug sensitivity using limited patient tumor samples.

Area of Science:

  • Biotechnology
  • Oncology
  • 3D Printing Applications

Background:

  • Personalized treatment strategies are crucial for non-small cell lung carcinoma (NSCLC) due to genetic mutations and acquired drug resistance.
  • Current limitations in evaluating drug sensitivity stem from the scarcity of patient-derived material.
  • Clinically relevant assay systems are needed for effective NSCLC therapy development.

Purpose of the Study:

  • To develop and validate a 3D-printed platform for culturing cancer cell spheroids.
  • To assess the utility of this platform for evaluating drug sensitivity in NSCLC.
  • To enable personalized drug screening using limited patient tumor samples.

Main Methods:

  • Utilized 3D printing to create molds for miniature agarose microwells (1000 per mold) with U-shaped bottoms.
  • Cultured three NSCLC cell lines (HCC4006, H1975, A549) within the 3D agarose microwells.
  • Evaluated spheroid size uniformity, viability, biomarker expression, and response to EGFR tyrosine kinase inhibitors (TKIs).

Main Results:

  • Achieved uniform spheroid size (CV <22%) and high viability (>83% after 1 week).
  • Demonstrated clinically relevant responses to gefitinib and osimertinib (EGFR TKIs).
  • Confirmed suitability for evaluating drug efficacy in NSCLC models.

Conclusions:

  • The 3D-printed microwell platform provides a robust system for *in vitro* cancer cell culture.
  • This platform is effective for drug sensitivity evaluation, particularly with limited tumor samples.
  • It supports the development of personalized NSCLC treatment strategies.

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