Dissecting Morphological and Functional Dynamics of Non-Tumorigenic and Triple-Negative Breast Cancer Cell Lines

Yazan A Almahdi1, Eva R Schwark1, Aidan J Mclaughlin1

  • 1Department of Natural Science, College of Arts Sciences and Letters, University of Michigan-Dearborn, Dearborn, Michigan, USA.

PubMed
Abstract

Insights

Triple-negative breast cancer (TNBC) cells show distinct morphological differences compared to normal cells. MDA-MB-231 TNBC cells exhibit higher motility and irregularity, contributing to their aggressive nature.

Area of Science:

  • Cell Biology
  • Cancer Research
  • Biophysics

Background:

  • Triple-negative breast cancer (TNBC) presents significant therapeutic challenges due to its aggressive behavior and lack of targeted treatments.
  • Understanding the distinct cellular characteristics of TNBC is vital for developing effective therapeutic strategies.

Purpose of the Study:

  • To compare the morphological and dynamic characteristics of non-tumorigenic MCF10A cells and aggressive MDA-MB-231 TNBC cells.
  • To utilize advanced analytical techniques for a detailed morphological assessment.

Main Methods:

  • Employed Principal Component Analysis (PCA) and t-Distributed Stochastic Neighbor Embedding (t-SNE) for data analysis.
  • Utilized digital holographic microscopy to analyze cellular features over time.
  • Quantified cell area, migration, motility, irregularity, and optical thickness.

Main Results:

  • Significant morphological disparities were observed between MCF10A and MDA-MB-231 cell lines.
  • MDA-MB-231 cells demonstrated increased motility, smaller size, and greater variability, indicative of invasive potential.
  • MCF10A cells showed larger size and regular migration, suggesting tissue stability.
  • Temporal analysis revealed consistent phenotypic behaviors, with MDA-MB-231 cells exhibiting higher optical thickness and irregularity.

Conclusions:

  • The distinct cellular dynamics highlight the adaptive mechanisms of TNBC cells.
  • These findings provide foundational insights into TNBC aggressiveness and progression.
  • The study offers a basis for future research into TNBC mechanisms and therapeutic targeting.

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