Development of a cancer metastasis-on-chip assay for high throughput drug screening

<p dir="ltr">Metastasis is the cause of most triple-negative breast cancer deaths, yet anti-metastatic therapeutics remain limited. To develop new therapeutics to prevent metastasis, pathophysiologically relevant assays that recapitulate tumor microenvironment is essential for diseas...

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Main Author: Lutfiye Yildiz Ozer (17732619) (author)
Other Authors: Hend Salah Fayed (17732622) (author), Johan Ericsson (49714) (author), Ayman Al Haj Zen (16614801) (author)
Published: 2024
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author Lutfiye Yildiz Ozer (17732619)
author2 Hend Salah Fayed (17732622)
Johan Ericsson (49714)
Ayman Al Haj Zen (16614801)
author2_role author
author
author
author_facet Lutfiye Yildiz Ozer (17732619)
Hend Salah Fayed (17732622)
Johan Ericsson (49714)
Ayman Al Haj Zen (16614801)
author_role author
dc.creator.none.fl_str_mv Lutfiye Yildiz Ozer (17732619)
Hend Salah Fayed (17732622)
Johan Ericsson (49714)
Ayman Al Haj Zen (16614801)
dc.date.none.fl_str_mv 2024-01-01T00:00:00Z
dc.identifier.none.fl_str_mv 10.3389/fonc.2023.1269376
dc.relation.none.fl_str_mv https://figshare.com/articles/journal_contribution/Development_of_a_cancer_metastasis-on-chip_assay_for_high_throughput_drug_screening/26316919
dc.rights.none.fl_str_mv CC BY 4.0
info:eu-repo/semantics/openAccess
dc.subject.none.fl_str_mv Biomedical and clinical sciences
Oncology and carcinogenesis
Pharmacology and pharmaceutical sciences
cancer metastasis
intravasation
organ-on-a chip
high content screening
targeted anti-cancer therapy
dc.title.none.fl_str_mv Development of a cancer metastasis-on-chip assay for high throughput drug screening
dc.type.none.fl_str_mv Text
Journal contribution
info:eu-repo/semantics/publishedVersion
text
contribution to journal
description <p dir="ltr">Metastasis is the cause of most triple-negative breast cancer deaths, yet anti-metastatic therapeutics remain limited. To develop new therapeutics to prevent metastasis, pathophysiologically relevant assays that recapitulate tumor microenvironment is essential for disease modeling and drug discovery. Here, we have developed a microfluidic metastasis-on-chip assay of the early stages of cancer metastasis integrated with the triple-negative breast cancer cell line (MDA-MB-231), stromal fibroblasts and a perfused microvessel. High-content imaging with automated quantification methods was optimized to assess the tumor cell invasion and intravasation within the model. Cell invasion and intravasation were enhanced when fibroblasts co-cultured with a breast cancer cell line (MDA-MB-231). However, the non-invasive breast cancer cell line, MCF7, remained non-invasive in our model, even in the presence of fibroblasts. High-content screening of a targeted anti-cancer therapy drug library was conducted to evaluate the drug response sensitivity of the optimized model. Through this screening, we identified 30 compounds that reduced the tumor intravasation by 60% compared to controls. Multi-parametric phenotypic analysis was applied by combining the data from the metastasis-on-chip, cell proliferation and 2D cell migration screens, revealing that the drug library was clustered into eight distinct groups with similar drug responses. Notably, MEK inhibitors were enriched in cluster cell invasion and intravasation. In contrast, drugs with molecular targets: ABL, KIT, PDGF, SRC, and VEGFR were enriched in the drug clusters showing a strong effect on tumor cell intravasation with less impact on cell invasion or cell proliferation, of which, Imatinib, a multi-kinase inhibitor targeting BCR-ABL/PDGFR/KIT. Further experimental analysis showed that Imatinib enhanced endothelial barrier stability as measured by trans-endothelial electrical resistance and significantly reduced the trans-endothelial invasion activity of tumor cells. Our findings demonstrate the potential of our metastasis-on-chip assay as a powerful tool for studying cancer metastasis biology, drug discovery aims, and assessing drug responses, offering prospects for personalized anti-metastatic therapies for triple-negative breast cancer patients.</p><h2>Other Information</h2><p dir="ltr">Published in: Frontiers in Oncology<br>License: <a href="https://creativecommons.org/licenses/by/4.0/" target="_blank">https://creativecommons.org/licenses/by/4.0/</a><br>See article on publisher's website: <a href="https://dx.doi.org/10.3389/fonc.2023.1269376" target="_blank">https://dx.doi.org/10.3389/fonc.2023.1269376</a></p>
eu_rights_str_mv openAccess
id Manara2_21d262a3555400667b7bc7fe97da48c5
identifier_str_mv 10.3389/fonc.2023.1269376
network_acronym_str Manara2
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oai_identifier_str oai:figshare.com:article/26316919
publishDate 2024
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spelling Development of a cancer metastasis-on-chip assay for high throughput drug screeningLutfiye Yildiz Ozer (17732619)Hend Salah Fayed (17732622)Johan Ericsson (49714)Ayman Al Haj Zen (16614801)Biomedical and clinical sciencesOncology and carcinogenesisPharmacology and pharmaceutical sciencescancer metastasisintravasationorgan-on-a chiphigh content screeningtargeted anti-cancer therapy<p dir="ltr">Metastasis is the cause of most triple-negative breast cancer deaths, yet anti-metastatic therapeutics remain limited. To develop new therapeutics to prevent metastasis, pathophysiologically relevant assays that recapitulate tumor microenvironment is essential for disease modeling and drug discovery. Here, we have developed a microfluidic metastasis-on-chip assay of the early stages of cancer metastasis integrated with the triple-negative breast cancer cell line (MDA-MB-231), stromal fibroblasts and a perfused microvessel. High-content imaging with automated quantification methods was optimized to assess the tumor cell invasion and intravasation within the model. Cell invasion and intravasation were enhanced when fibroblasts co-cultured with a breast cancer cell line (MDA-MB-231). However, the non-invasive breast cancer cell line, MCF7, remained non-invasive in our model, even in the presence of fibroblasts. High-content screening of a targeted anti-cancer therapy drug library was conducted to evaluate the drug response sensitivity of the optimized model. Through this screening, we identified 30 compounds that reduced the tumor intravasation by 60% compared to controls. Multi-parametric phenotypic analysis was applied by combining the data from the metastasis-on-chip, cell proliferation and 2D cell migration screens, revealing that the drug library was clustered into eight distinct groups with similar drug responses. Notably, MEK inhibitors were enriched in cluster cell invasion and intravasation. In contrast, drugs with molecular targets: ABL, KIT, PDGF, SRC, and VEGFR were enriched in the drug clusters showing a strong effect on tumor cell intravasation with less impact on cell invasion or cell proliferation, of which, Imatinib, a multi-kinase inhibitor targeting BCR-ABL/PDGFR/KIT. Further experimental analysis showed that Imatinib enhanced endothelial barrier stability as measured by trans-endothelial electrical resistance and significantly reduced the trans-endothelial invasion activity of tumor cells. Our findings demonstrate the potential of our metastasis-on-chip assay as a powerful tool for studying cancer metastasis biology, drug discovery aims, and assessing drug responses, offering prospects for personalized anti-metastatic therapies for triple-negative breast cancer patients.</p><h2>Other Information</h2><p dir="ltr">Published in: Frontiers in Oncology<br>License: <a href="https://creativecommons.org/licenses/by/4.0/" target="_blank">https://creativecommons.org/licenses/by/4.0/</a><br>See article on publisher's website: <a href="https://dx.doi.org/10.3389/fonc.2023.1269376" target="_blank">https://dx.doi.org/10.3389/fonc.2023.1269376</a></p>2024-01-01T00:00:00ZTextJournal contributioninfo:eu-repo/semantics/publishedVersiontextcontribution to journal10.3389/fonc.2023.1269376https://figshare.com/articles/journal_contribution/Development_of_a_cancer_metastasis-on-chip_assay_for_high_throughput_drug_screening/26316919CC BY 4.0info:eu-repo/semantics/openAccessoai:figshare.com:article/263169192024-01-01T00:00:00Z
spellingShingle Development of a cancer metastasis-on-chip assay for high throughput drug screening
Lutfiye Yildiz Ozer (17732619)
Biomedical and clinical sciences
Oncology and carcinogenesis
Pharmacology and pharmaceutical sciences
cancer metastasis
intravasation
organ-on-a chip
high content screening
targeted anti-cancer therapy
status_str publishedVersion
title Development of a cancer metastasis-on-chip assay for high throughput drug screening
title_full Development of a cancer metastasis-on-chip assay for high throughput drug screening
title_fullStr Development of a cancer metastasis-on-chip assay for high throughput drug screening
title_full_unstemmed Development of a cancer metastasis-on-chip assay for high throughput drug screening
title_short Development of a cancer metastasis-on-chip assay for high throughput drug screening
title_sort Development of a cancer metastasis-on-chip assay for high throughput drug screening
topic Biomedical and clinical sciences
Oncology and carcinogenesis
Pharmacology and pharmaceutical sciences
cancer metastasis
intravasation
organ-on-a chip
high content screening
targeted anti-cancer therapy