Abstract | PURPOSE: METHODS: With the knock-down of USP22, the changes of cellular proliferation, cell cycle, cell apoptosis, and major vault protein (MVP) expression were investigated. Furthermore, a tumor xenograft model in nude mice was injected with USP22 miRNA silencing vector and the immunohistochemical staining was performed to evaluate the USP22 expression in the tumor. RESULTS: The knock-down of USP22 protein expression by miRNA resulted in the inhibition of cellular proliferation, the accumulation of cells in the G1 phase, the reduction of apoptosis, and the down-regulation of MVP expression. Furthermore, with orthotopic mice as a model, tumor growth was suppressed when USP22 miRNA silencing vector was injected. Immunohistochemical analyses of tumor sections revealed that USP22 expression in animals decreased when USP22 expression was inhibited by miRNA. CONCLUSION: These results support the hypothesis that USP22 plays a crucial role in tumor formation and growth by regulating cell proliferation with USP22-dependent signaling pathway. Furthermore, USP22 acts as a major transcriptional factor to regulate MVP drug resistant gene. Taken together, targeting USP22 may offer additional possibilities in cancer therapy.
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Authors | Hui Xu, Yan-Long Liu, Yan-Mei Yang, Xin-Shu Dong |
Journal | International journal of colorectal disease
(Int J Colorectal Dis)
Vol. 27
Issue 1
Pg. 21-30
(Jan 2012)
ISSN: 1432-1262 [Electronic] Germany |
PMID | 21773699
(Publication Type: Journal Article)
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Chemical References |
- MicroRNAs
- Vault Ribonucleoprotein Particles
- major vault protein
- Thiolester Hydrolases
- Ubiquitin Thiolesterase
- Usp22 protein, human
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Topics |
- Animals
- Apoptosis
(genetics)
- Cell Proliferation
- Cell Survival
- Colorectal Neoplasms
(enzymology, genetics, pathology)
- Down-Regulation
(genetics)
- G1 Phase
(genetics)
- Gene Expression Regulation, Neoplastic
- Gene Knockdown Techniques
- HCT116 Cells
- Humans
- Mice
- Mice, Nude
- MicroRNAs
(metabolism)
- RNA Interference
- S Phase
(genetics)
- Thiolester Hydrolases
(genetics, metabolism)
- Transfection
- Ubiquitin Thiolesterase
- Vault Ribonucleoprotein Particles
(metabolism)
- Xenograft Model Antitumor Assays
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