| Literature DB >> 33290947 |
Md Shahjahan Molla1, Dinesh R Katti2, Kalpana S Katti3.
Abstract
Prostate cancer exhibits a propensity to metastasize to the bone, which often leads to fatality. Bone metastasis is characterized by complex biochemical, morphological, pathophysiological, and genetic changes to cancer cells as they colonize at bone sites. In this study, we report the evaluation of MDA PCa2b prostate cancer cells' nanomechanical properties during the mesenchymal-to-epithelial transition (MET) and during disease progression at the metastatic site. Bone-mimetic tissue-engineered 3D nanoclay scaffolds have been used to create in vitro metastatic site for prostate cancer. A significant softening of the prostate cancer cells during MET and further softening as disease progression occurs at metastasis is also reported. The significant reduction in elastic modulus of prostate cancer cells during MET was attributed to actin reorganization and depolymerization. This study provides input towards direct nanomechanical measurements to evaluate the time evolution of cells' mechanical behavior in tumors at bone metastasis site.Entities:
Keywords: Mechanobiology; Metastasis; Nanoclay; Nanomechanics; Prostate cancer; Scaffolds
Mesh：
Year: 2020 PMID： 33290947 PMCID： PMC8281967 DOI： 10.1016/j.jbiomech.2020.110142
Source DB: PubMed Journal: J Biomech ISSN： 0021-9290 Impact factor: 2.712