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Physical confinement during cancer cell migration triggers therapeutic resistance and cancer stem cell-like behavior.


ABSTRACT: Metastasized cancer cells have an increased resistance to therapies leading to a drastic decrease in patient survival rates. However, our understanding of the cause for this enhanced resistance is lacking. In this study, we report that physically tight confinement during cancer cell migration triggers therapeutic resistance and induces cancer stem cell-like behavior including up-regulation in efflux proteins and in cancer stem cell related markers. Moreover, the re-localization of Yes-associated protein (YAP) to the cell nucleus indicated an elevated level of cytoskeletal tension. The increased cytoskeletal tension suggested that mechanical interactions between cancer cells and tight surroundings during metastasis is one of the factors that contributes to therapeutic resistance and acquisition of cancer stem cell (CSC) like features. With this system and supporting data, we are able to study cells with therapeutic resistance and CSC-like properties for the future purpose of developing new strategies for the treatment of metastatic cancer.

SUBMITTER: Shen Q 

PROVIDER: S-EPMC8112468 | biostudies-literature | 2021 May

REPOSITORIES: biostudies-literature

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Physical confinement during cancer cell migration triggers therapeutic resistance and cancer stem cell-like behavior.

Shen Qionghua Q   Hill Tamara T   Cai Xue X   Bui Loan L   Barakat Rami R   Hills Emily E   Almugaiteeb Turki T   Babu Anish A   Mckernan Patrick H PH   Zalles Michelle M   Battiste James D JD   Kim Young-Tae YT  

Cancer letters 20210225


Metastasized cancer cells have an increased resistance to therapies leading to a drastic decrease in patient survival rates. However, our understanding of the cause for this enhanced resistance is lacking. In this study, we report that physically tight confinement during cancer cell migration triggers therapeutic resistance and induces cancer stem cell-like behavior including up-regulation in efflux proteins and in cancer stem cell related markers. Moreover, the re-localization of Yes-associated  ...[more]

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