Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/11423
Title: On-chip determination of tissue-specific metastatic potential of breast cancer cells
Authors: Firatligil-Yildirir, Burcu
Bati-Ayaz, Gizem
Tahmaz, Ismail
Bilgen, Muge
Pesen-Okvur, Devrim
Yalcin-Ozuysal, Ozden
Keywords: breast cancer
extravasation
invasion
lab-on-a-chip
metastasis
Issue Date: 2021
Publisher: Wiley
Abstract: Metastasis is one of the major obstacles for breast cancer patients. Limitations of current models demand the development of custom platforms to predict metastatic potential and homing choices of cancer cells. Here, two organ-on-chip platforms, invasion/chemotaxis (IC-chip) and extravasation (EX-chip) were used for the quantitative assessment of invasion and extravasation towards specific tissues. Lung, liver and breast microenvironments were simulated in the chips using tissue-specific cells embedded in matrigel. In the IC-chip, invasive MDA-MB-231, but not noninvasive MCF-7 breast cancer cells invaded into lung and liver microenvironments. In the EX-chip, MDA-MB-231 cells extravasated more into the lung compared to the liver and breast microenvironments. In addition, lung-specific MDA-MB-231 clone invaded and extravasated into the lung microenvironment more efficiently than the bone-specific clone. Both invasion/chemotaxis and extravasation results were in agreement with published clinical data. Collectively, our results show that IC-chip and EX-chip, simulating tissue-specific microenvironments, can distinguish different in vivo metastatic phenotypes, in vitro. Determination of tissue-specific metastatic potential of breast cancer cells is expected to improve diagnosis and help select the ideal therapy.
URI: https://doi.org/10.1002/bit.27855
https://hdl.handle.net/11147/11423
ISSN: 0006-3592
1097-0290
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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