IndraLab

Statements



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"USP28 contributes to the proliferation and metastasis of gastric cancer."

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"Through the miR‐500a‐5p/ubiquitin specific peptidase 28 (USP28) axis, exosomal miR‐500a‐5p in CAFs could promote cancer cell proliferation, EMT, and metastasis [57]."

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"MiR-500a-5p was transferred from CAFs to the cancer cells, and subsequently promoted proliferation and metastasis by binding to ubiquitin specific peptidase 28 (USP28)."

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"In NCCIT cells, wound healing assays and Matrigel cell invasion assays revealed that the USP28 activates the process of metastasis through its deubiquitination of Lin28A [74]."

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"Pard3 deletion led to the up-regulation of USP28, which promoted BC migration and migration via Snail1 stabilization.Given its essential role in tumor metastasis and EMT, Snail1 is considered a key regulator of aggressive phenotypes in tumors."

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"USP28 is a member of deubiquitinase family, and the aberrant expression and functional dysregulation of USP28 might lead to the development and metastasis of malignant tumors [12,13] ."