Label-free drug response evaluation of human derived tumor spheroids using three-dimensional dynamic optical

Ibrahim Abd El-Sadek1,2, Larina Tzu-Wei Shen3, Tomoko Mori3

  • 1Computational Optics Group, University of Tsukuba, Tsukuba, Ibaraki, 305-8573, Japan.

Scientific Reports
|September 16, 2023
PubMed

Insights

Dynamic optical coherence tomography (D-OCT) offers label-free assessment of anti-cancer drug responses in tumor spheroids. This method visualizes distinct drug-induced patterns, showing its potential for personalized cancer drug testing.

Area of Science:

  • Biomedical Optics
  • Cancer Research
  • Drug Discovery

Background:

  • Accurate assessment of anti-cancer drug efficacy is crucial for effective cancer treatment.
  • Tumor spheroids serve as advanced in vitro models for studying drug responses.
  • Label-free imaging techniques offer advantages by avoiding exogenous agents.

Purpose of the Study:

  • To demonstrate label-free assessment of drug response patterns in different tumor spheroids using dynamic optical coherence tomography (D-OCT).
  • To evaluate the feasibility of D-OCT for anti-cancer drug testing.
  • To investigate differential responses of breast (MCF-7) and colon (HT-29) cancer spheroids to paclitaxel and SN-38.

Main Methods:

  • Utilized a swept-source OCT microscope with a repeated raster scanning protocol.
  • Applied logarithmic intensity variance (LIV) and OCT correlation decay speed (OCDS) algorithms for image analysis.
  • Treated MCF-7 and HT-29 spheroids with varying concentrations (0-10 microM) of paclitaxel and SN-38 over 1, 3, and 6 days.

Main Results:

  • LIV and OCDS imaging successfully visualized distinct drug-response patterns for MCF-7 and HT-29 spheroids.
  • Quantification of spheroid morphology, LIV, and OCDS revealed differential time-courses based on spheroid and drug type.
  • Observed variations suggest potentially different drug action mechanisms.

Conclusions:

  • D-OCT is a feasible technique for label-free evaluation of drug response patterns in various tumor spheroids and drug types.
  • The study demonstrates D-OCT's potential as a tool for anti-cancer drug screening and testing.
  • Findings support the utility of D-OCT in understanding differential drug effects and mechanisms.

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