IndraLab

Statements

USP53 activates epithelial to mesenchymal transition. 4 / 4
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"Additionally, the knockdown of USP53 suppressed proliferation, EMT, and metastasis and enhanced the paclitaxel response of TNBC cells."
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"Because upregulation of USP53 promoted proliferation, migration, invasion, and EMT in TNBC, we investigated whether this was due to the regulation of CRKL by USP53."
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"Taken together, USP53 promotes metastasis and EMT in TNBC."
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"Functionally, USP53 promotes TNBC cell proliferation, migration, invasion, and epithelial-mesenchymal transition (EMT)."
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