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We are analyzing https://www.nature.com/articles/s41598-017-17177-5.

Title:
Three-dimensional organotypic matrices from alternative collagen sources as pre-clinical models for cell biology | Scientific Reports
Description:
Organotypic co-cultures bridge the gap between standard two-dimensional culture and mouse models. Such assays increase the fidelity of pre-clinical studies, to better inform lead compound development and address the increasing attrition rates of lead compounds within the pharmaceutical industry, which are often a result of screening in less faithful two-dimensional models. Using large-scale acid-extraction techniques, we demonstrate a step-by-step process to isolate collagen I from commercially available animal byproducts. Using the well-established rat tail tendon collagen as a benchmark, we apply our novel kangaroo tail tendon collagen as an alternative collagen source for our screening-ready three-dimensional organotypic co-culture platform. Both collagen sources showed equal applicability for invasive, proliferative or survival assessment of well-established cancer models and clinically relevant patient-derived cancer cell lines. Additional readouts were also demonstrated when comparing these alternative collagen sources for stromal contributions to stiffness, organization and ultrastructure via atomic force microscopy, second harmonic generation imaging and scanning electron microscopy, among other vital biological readouts, where only minor differences were found between the preparations. Organotypic co-cultures represent an easy, affordable and scalable model to investigate drug responses within a physiologically relevant 3D platform.
Website Age:
30 years and 10 months (reg. 1994-08-11).

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Keywords {🔍}

pubmed, article, collagen, google, scholar, cas, cancer, tail, cell, matrix, kangaroo, organotypic, rat, cells, matrices, fig, central, nature, staining, journal, assessment, invasion, analysis, fibroblasts, pancreatic, stromal, performed, preclinical, microscopy, research, growth, breast, ads, platform, line, significant, models, imaging, ecm, scale, bars, biology, assay, protein, force, preparations, drug, metastasis, human, days,

Topics {✒️}

nature portfolio privacy policy /timpsonlab/shg-quantification-tools 10 mm stock solutions advertising open source software olympus u-pot polarizer inhibits egf-induced invasion reprints author information authors large-scale acid-extraction techniques triple-negative breast cancer overcomes growth arrest/senescence patient-derived cell lines29 cubic b-spline interpolation pre-clinical testing grounds patient-derived cell line quantitative real-time pcr real-time quantitative pcr tmc anti-vibration table inexpensive pre-clinical platform high inter-batch variability patient-derived tumour xenografts original author breast cancer research picro-sirius red fba invasive index calculated beta-catenin activation tyrosine kinase inhibitor reducing batch-specific variation central factors contributing clinical cancer research nature medicine 23 nature medicine 19 lox/hypoxia axis reverses irrelevant cell-based models future pre-clinical investigations drug-dependent dynamic regulation taking cell-matrix adhesions nature reviews nature communications 5 nature communications 8 nature communications 2 tyrosine phosphatase ptpn14 melanoma cell-derived factors multiphoton-excited native fluorescence nature protocols 1 nature protocols 7 nature protocols 2 nonpolarized signaling reveals

Questions {❓}

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Schema {🗺️}

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         headline:Three-dimensional organotypic matrices from alternative collagen sources as pre-clinical models for cell biology
         description:Organotypic co-cultures bridge the gap between standard two-dimensional culture and mouse models. Such assays increase the fidelity of pre-clinical studies, to better inform lead compound development and address the increasing attrition rates of lead compounds within the pharmaceutical industry, which are often a result of screening in less faithful two-dimensional models. Using large-scale acid-extraction techniques, we demonstrate a step-by-step process to isolate collagen I from commercially available animal byproducts. Using the well-established rat tail tendon collagen as a benchmark, we apply our novel kangaroo tail tendon collagen as an alternative collagen source for our screening-ready three-dimensional organotypic co-culture platform. Both collagen sources showed equal applicability for invasive, proliferative or survival assessment of well-established cancer models and clinically relevant patient-derived cancer cell lines. Additional readouts were also demonstrated when comparing these alternative collagen sources for stromal contributions to stiffness, organization and ultrastructure via atomic force microscopy, second harmonic generation imaging and scanning electron microscopy, among other vital biological readouts, where only minor differences were found between the preparations. Organotypic co-cultures represent an easy, affordable and scalable model to investigate drug responses within a physiologically relevant 3D platform.
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      headline:Three-dimensional organotypic matrices from alternative collagen sources as pre-clinical models for cell biology
      description:Organotypic co-cultures bridge the gap between standard two-dimensional culture and mouse models. Such assays increase the fidelity of pre-clinical studies, to better inform lead compound development and address the increasing attrition rates of lead compounds within the pharmaceutical industry, which are often a result of screening in less faithful two-dimensional models. Using large-scale acid-extraction techniques, we demonstrate a step-by-step process to isolate collagen I from commercially available animal byproducts. Using the well-established rat tail tendon collagen as a benchmark, we apply our novel kangaroo tail tendon collagen as an alternative collagen source for our screening-ready three-dimensional organotypic co-culture platform. Both collagen sources showed equal applicability for invasive, proliferative or survival assessment of well-established cancer models and clinically relevant patient-derived cancer cell lines. Additional readouts were also demonstrated when comparing these alternative collagen sources for stromal contributions to stiffness, organization and ultrastructure via atomic force microscopy, second harmonic generation imaging and scanning electron microscopy, among other vital biological readouts, where only minor differences were found between the preparations. Organotypic co-cultures represent an easy, affordable and scalable model to investigate drug responses within a physiologically relevant 3D platform.
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         Cancer models
         Extracellular matrix
         Science
         Humanities and Social Sciences
         multidisciplinary
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