IndraLab

Statements



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"In summary, in vitro assays indicated that USP11 enhances CRC cell proliferation, migration, and invasion, but showed no effect on apoptosis.3.3 USP11 enhances tumorigenesis and liver metastasis of CRC in vivo."

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"The authors postulated that USP11 up-regulates and augments the ability of proliferation, invasion, migration and collagen deposition of keloid-derived fibroblasts (KFBs) through deubiquitinating TGF-β receptor II (TβRII)."

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"Taken together, these data indicate that USP11 overexpression may be relevant with the tumorigenesis and progression of CRC.3.2 USP11 promotes CRC cell proliferation, migration, and invasion in vitro."

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"This suggested that USP11 promotes CRC invasion and metastasis."

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"USP11 elevates the ability of proliferation, collagen deposition, invasion and migration of keloid-derived fibroblasts by deubiquitinating TβRII."

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"Also, USP11 had been confirmed to accelerate proliferation, invasion and migration in keloid derived-fibroblasts ."

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"Moreover, in vitro and in vivo experiments confirmed that USP11 could promote the migration and invasion of HCC cell."

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"The combination of USP11 overexpression and BLM treatment produced increased cell migration and invasion, compared with cells treated with BLM alone (Figure 5G and 5H)."

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"USP11 promotes HCC cell survival, invasion, and metastatic potency in vitro and in vivo."

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"Transwell assays indicated that silencing USP11 inhibited the invasion and migration of HCC cells (Fig. 5A, Figure S2E), while overexpressing USP11 promoted these processes (Fig. 5B)."

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"USP11 promotes the proliferation, migration, and invasion of CRC cells by modulating IGF2BP3 stability [84]."

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"USP1, OUTB1, and USP11 induced migration, invasion, and metastasis through Snail (Figure 2B) [109,111,112]."