Abstract

The invasion of cancer is brought about by continuous interaction of malignant cells with their surrounding tissue microenvironment. Investigating the remodeling of local extracellular matrix (ECM) by invading cells can thus provide fundamental insights into the dynamics of cancer progression. In this paper, we use an active untethered nanomechanical tool, realized as magnetically driven nanomotors, to locally probe a 3D tissue culture environment. We observed that nanomotors preferentially adhere to the cancer‐proximal ECM and magnitude of the adhesive force increased with cell lines of higher metastatic ability. We experimentally confirmed that sialic acid linkage specific to cancer‐secreted ECM makes it differently charged, which causes this adhesion. In an assay consisting of both cancerous and non‐cancerous epithelia, that mimics the in vivo histopathological milieu of a malignant breast tumor, we find that nanomotors preferentially decorate the region around the cancer cells.

Highlights

  • Fabrication of thin nanomotors: To fabricate thin nanomotors, it was necessary to reduce the seed layer size while maintaining enough distance between subsequent seeds to allow shadowing during evaporation

  • This was used as the seed layer for Glancing Angle Deposition (GLAD) of silica in which the magnetic material made of iron and cobalt powder mixed in 1:1 (w/w) ratio was integrated inline during the shadow growth

  • All the cells were maintained in a humidified chamber at 370 C temperature and 5% carbon dioxide. 3D culture and experimental procedure: In case of 3D monoculture, 5×104 cells were mixed in 50 μl of reconstituted Basement Membrane (rBM) (Corning, 354230) and allowed to solidify at 370 C temperature and 5% carbon dioxide in a humidified chamber

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Summary

Supporting Information

Nanomotors Sense Local Physicochemical Heterogeneities in Tumor Microenvironments**. Anie_202008681_sm_miscellaneous_information.pdf anie_202008681_sm_M1.mp[4] anie_202008681_sm_M2.mp[4] anie_202008681_sm_M3.mp[4] anie_202008681_sm_M4.mp[4] anie_202008681_sm_M5.mp[4]

Materials and methods
Supporting information
Immortalized mammary epithelial cell line
Full Text
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