Tumor Models | Farcast biodynamics
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TRUTUMOR TUMOR MODELS

Human Relevant Data & Biosignatures

Farcast's extensively published models ensure that tissue fragments are optimally sized, maintaining the equilibrium between stromal, tumor and immune components and retaining the spatial contexture of the original tumor microenvironment. Such living, near native, heterogeneous tumor systems are ideal for determining true treatment impact and predicting tumor and immune responses

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Farcast's technology comprehensively combines multimodal data from every tumor processed with available multiomics and clinical information. The AI (artificial intelligence) enabled technology computes response biosignatures of treatments with higher precision that truly elucidate the complexities of tumor responses

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Application of such true perturbation based human biosignatures leads to a much more precise identification of responder phenotypes than traditional biomarkers or baseline signatures

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Test Combination Therapies

Develop combination strategy and test synergy with existing treatments

Scout New Indications

Expand the range of indications of your pipeline

Evaluate Mechanism of Action

Gain confidence in the mechanism of your therapeutic candidate 

Discover Predictive Biosignatures

Optimal patient stratification for enhanced response rates

Hispathology
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HISTOPATHOLOGY

Morphological assessment of mechanistic response of drug to assess proliferation, cell death and immune cell infiltration induced by treatment

GENE EXPRESSION

Measurement of differential gene expression resulting from therapeutic intervention

 

Patient cohort stratification discovery with baseline gene expression

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Farcast proprietary images

PanCK

Fox P3

CD8

SPATIAL BIOLOGY

Live imaging that offers a comprehensive evaluation of true tumor microenvironment

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Multiplex immunofluorescence techniques that help visualization of the spatial distribution of different sub-population of immune and cancer cells in the original human tumor microenvironment

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Assessment of changes in spatial biology caused by therapeutic intervention in the treated tumor microenvironment

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FLOWCYTOMETRY

Precise measurement and characterization of diverse immune cell populations within the tumor microenvironment

 

Customized panels for assessment of specific immune cell type activity indicative of therapy response

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CYTOKINE PROFILING

Flexible, multiplexed quantitative evaluation of cytokines/chemokines released due to therapeutic intervention 

 

Immune effector cells for assessing early response in tumor fragments in response to drug exposure

KINETIC ASSAYS

Discrete time course measurements to understand the metabolic state and viability of explants in the culture system for up to 72 hours

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