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Metastasis02:30

Metastasis

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Metastasis is the spread of cancer cells from the original site to distant locations in the body. Cancer cells can spread via blood vessels (hematogenous) as well as lymph vessels in the body.
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...
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Modeling and Imaging 3-Dimensional Collective Cell Invasion
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Single-cell morphology encodes metastatic potential.

Pei-Hsun Wu1,2, Daniele M Gilkes1,3, Jude M Phillip2

  • 1Johns Hopkins Physical Sciences-Oncology Center, The Johns Hopkins University, Baltimore, MD 21218, USA.

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|February 4, 2020
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Summary
This summary is machine-generated.

Cell morphology analysis reveals distinct, heritable traits in breast cancer clones. These morphological differences predict tumor growth and metastasis, offering a new method for in vivo cancer phenotyping.

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Area of Science:

  • Cancer research
  • Cell biology
  • Genomics

Background:

  • Precision medicine aims to tailor treatments using multidimensional patient data.
  • Cell morphology reflects a cell's functional state and molecular underpinnings.
  • Quantitative cell morphology analysis can provide insights into cellular function.

Purpose of the Study:

  • To investigate the relationship between cell morphology and functional phenotypes in breast cancer.
  • To determine if morphological traits are heritable and associated with genomic and transcriptomic profiles.
  • To assess the predictive power of cell morphology for tumorigenic and metastatic potential in vivo.

Main Methods:

  • Measured 216 morphological features from over 30,000 breast cancer cells.
  • Established and analyzed single cell-derived clones (SCCs) from parental breast cancer cells.
  • Utilized unsupervised clustering analysis to classify SCCs based on morphology.
  • Validated findings using multiple in vivo mouse models of breast cancer.

Main Results:

  • Single cell-derived clones exhibited distinct and heritable morphological traits.
  • Morphological traits were associated with genomic (ploidy) and transcriptomic phenotypes.
  • Morphological classes predicted distinct tumorigenic and metastatic potentials in vivo.
  • Quantitative morpho-profiling effectively phenotyped cancer cell function.

Conclusions:

  • Cell morphology is a heritable trait linked to functional and genomic phenotypes in breast cancer.
  • In vitro quantitative morpho-profiling can predict in vivo cancer behavior.
  • Morpho-profiling offers a potentially convenient and economical method for cancer phenotyping.