Diverse Ways to Control p27Kip1 Function: miRNAs Come into Play
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Summary
The difficulties interpreting the data from available computer algorithms are reviewed, the pros and cons of the genetic screening method are critically addressed, and how miRNAs could be involved in the regulation of p27 in both normal and malignant conditions are argued.
- Type
- review
- Published
- 2007-11-15
- Cited by
- 63
- References
- 108
- Access
- Open access
- OpenAlex
- https://openalex.org/W2001769314
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:22887986
Keywords
Biology, microRNA, Computational biology, Function (biology), Gene
References
- p27(Kip1) ubiquitination and degradation is regulated by the SCF(Skp2) complex through phosphorylated Thr187 in p27.
- Pten and p27KIP1 cooperate in prostate cancer tumor suppression in the mouse
- MicroRNA genes are transcribed by RNA polymerase II
- The murine gene p27Kip1 is haplo-insufficient for tumour suppression
- p45SKP2 promotes p27Kip1 degradation and induces S phase in quiescent cells
- The cell-cycle regulatory protein Cks1 is required for SCFSkp2-mediated ubiquitinylation of p27
- Are all cancer genes equal?
- Oncogenic kinase signalling
- Regulation of the Cdk inhibitor p27 and its deregulation in cancer
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- Both natural and designed micro RNAs can inhibit the expression of cognate mRNAs when expressed in human cells.
- Cell Cycle Control: A Complex Issue
- 14-3-3 suppresses the nuclear localization of threonine 157-phosphorylated p27(Kip1).
- The role of microRNA genes in papillary thyroid carcinoma.
- c-Myc-regulated microRNAs modulate E2F1 expression
- Cytoplasmic ubiquitin ligase KPC regulates proteolysis of p27Kip1 at G1 phase
- A Role for the RNase III Enzyme DCR-1 in RNA Interference and Germ Line Development in Caenorhabditis elegans
- Translational Control of p27Kip1 Accumulation During the Cell Cycle
- The nuclear RNase III Drosha initiates microRNA processing
- Cytoplasmic relocalization and inhibition of the cyclin-dependent kinase inhibitor p27Kip1 by PKB/Akt-mediated phosphorylation in breast cancer
Cited by
- Regulation of p27(kip1) mRNA expression by microRNAs.
- The transcription factor FOXM1 (Forkhead box M1): proliferation-specific expression, transcription factor function, target genes, mouse models, and normal biological roles.
- microRNAs in cancer: from bench to bedside.
- REGULATION OF MAMMARY GLAND DEVELOPMENT AND TUMORIGENESIS BY 14-3-3 ZETA
- MicroRNA miR‐24 promotes cell proliferation by targeting the CDKs inhibitors p27Kip1 and p16INK4a
- A Novel Mutation in the Upstream Open Reading Frame of the CDKN1B Gene Causes a MEN4 Phenotype
- Profilin-1 overexpression inhibits proliferation of MDA-MB-231 breast cancer cells partly through p27kip1 upregulation
- Control of cell proliferation pathways by microRNAs
- IKK-β/NFκB p65 Mediates p27kip1 Protein Degradation in Arsenite Response
- [p53 and p27 gene expression in subserosal gallbladder carcinoma].
- Pumilio turns on microRNA function
- RETRACTED ARTICLE: MIR221/MIR222-driven post-transcriptional regulation of P27KIP1 and P57KIP2 is crucial for high-glucose- and AGE-mediated vascular cell damage
- Genome-wide siRNA Screen Identifies the Radiosensitizing Effect of Downregulation of MASTL and FOXM1 in NSCLC
- Long non-coding RNA UCA1 promotes breast tumor growth by suppression of p27 (Kip1)
- The regulatory loop of COMP1 and HNF-4-miR-150-p27 in various signaling pathways
- p27 as Jekyll and Hyde: Regulation of cell cycle and cell motility
- miR-340 inhibits tumor cell proliferation and induces apoptosis by targeting multiple negative regulators of p27 in non-small cell lung cancer
- The Cdk inhibitor p27 in human cancer: prognostic potential and relevance to anticancer therapy
- Localization‐ and mutation‐dependent microRNA (miRNA) expression signatures in gastrointestinal stromal tumours (GISTs), with a cluster of co‐expressed miRNAs located at 14q32.31
- Immunohistochemical expression of p27(kip1) in metastatic laryngeal squamous cell carcinoma.
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