期刊
ONCOGENE
卷 32, 期 40, 页码 4758-4765出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/onc.2012.497
关键词
PIR2; Rnf144B; p63; p21(WAF1); squamous cell carcinoma (SCC); skin
资金
- University of Southampton
- Medical Research Council, UK
- 'Alleanza contro il Cancro' [ACC12]
- MIUR/PRIN [RBIP06LCA9_0023]
- AIRC [2008-2010_33-08]
- Italian Human ProteomeNet RBRN07BMCT
- Medical Research Council [MC_U132670600] Funding Source: researchfish
- MRC [MC_U132670600] Funding Source: UKRI
Delta Np63 is a transcription factor that is critical for the development of stratified epithelia and is overexpressed or amplified in >80% of squamous cell carcinomas (SCCs). We identified the RING finger E3 ubiquitin ligase PIR2/Rnf144b as a direct transcriptional target of Delta Np63 alpha and showed that its expression parallels that of Delta Np63 alpha in keratinocytes, SCC cell lines and SCCs. We used primary keratinocytes as a model system to investigate the function of PIR2/Rnf144b in stratified epithelia. Depletion of PIR2/Rnf144b severely impaired keratinocyte proliferation and differentiation, associated with accumulation of p21(WAF1/CIP1); a known target of PIR2/Rnf144b. More importantly, we found that PIR2/Rnf144b binds and mediates proteasomal degradation of Delta Np63 alpha, generating a hitherto unknown auto-regulatory feedback loop. These findings substantiate PIR2/Rnf144b as a potentially critical component of epithelial homeostasis, acting downstream of Delta Np63 alpha to regulate cellular levels of p21(WAF1/CIP1) and Delta Np63 alpha.
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