3D Spheroids Propel Tumor Characterization

Shengli Li1, Zhao Zhang1, Leng Han2

  • 1Department of Biochemistry and Molecular Biology, McGovern Medical School at The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.

Trends in Cancer
|May 20, 2020
PubMed

Insights

Researchers used 3D lung cancer spheroids and clustered regularly interspaced short palindromic repeats (CRISPR) screening to identify new cancer targets. This 3D model better mimics tumors than 2D models, revealing carboxypeptidase D (CPD) as a potential therapeutic target.

Area of Science:

  • Oncology
  • Genetics
  • Biotechnology

Background:

  • Accurately modeling in vivo tumors is crucial for understanding cancer driver gene functions.
  • Traditional 2D cell culture models have limitations in replicating the complex tumor microenvironment.

Purpose of the Study:

  • To evaluate the utility of 3D lung cancer spheroids for large-scale clustered regularly interspaced short palindromic repeats (CRISPR) screening.
  • To identify novel cancer driver genes and potential therapeutic targets using an advanced 3D screening model.

Main Methods:

  • Implementation of large-scale CRISPR screening.
  • Utilizing 3D lung cancer spheroids as an advanced cancer model.
  • Comparison of 3D spheroids versus 2D monolayers for screening efficacy.

Main Results:

  • 3D spheroids demonstrated significant advantages over 2D monolayers for CRISPR screening.
  • Novel cancer driver genes were identified through the screening process.
  • Carboxypeptidase D (CPD) was identified as a promising novel therapeutic target.

Conclusions:

  • 3D lung cancer spheroids provide a more effective platform for functional cancer genomics screening.
  • The study highlights the potential of CPD as a therapeutic target for lung cancer treatment.

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