Accumulation of inactive p53 protein in oral squamous cell carcinoma: stabilization by protein interaction. (30th November 2012)
- Record Type:
- Journal Article
- Title:
- Accumulation of inactive p53 protein in oral squamous cell carcinoma: stabilization by protein interaction. (30th November 2012)
- Main Title:
- Accumulation of inactive p53 protein in oral squamous cell carcinoma: stabilization by protein interaction
- Authors:
- Francis, Geo
Dileep Kumar, U
Nalinakumari, KR
Jayasree, K
Kannan, S - Abstract:
- <abstract abstract-type="main" id="eos12007-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Our previous study showed that p53 protein is accumulated in &gt;60% of cases of oral squamous cell carcinoma (OSCC) and its overexpression is related to poor prognosis. However, the mechanism behind this is still elusive. The present study attempts to dissect p53 alterations at various levels from gene to function in tumor biopsies to understand whether molecular alterations have any relationship with the accumulation of p53 protein in OSCC. Protein‐stabilizing mutations were observed in only 13.8% of the samples. Neither p53 polymorphisms nor human papillomavirus (HPV) infection (&lt;2%) has any major role in augmented expression of p53 protein. Analysis of the p53 transcript demonstrated that alteration in the level of <italic>p53 </italic>mRNA (10%) is not the major mechanistic cause for accumulation of p53 protein, and p21 transcript status showed that the overexpressed p53 protein is functionally inactive. Immunoprecipitation studies demonstrated that the known interactors of p53, such as MDM2 and HSP70, have no significant role in stabilizing p53 and the significant presence of some unknown interactors, sequestering p53, and leading to the aberrant accumulation of p53. Our study suggests that overexpression of inactive p53 protein could be manifested as a result of sequestering from degradation by an unknown interacting protein rather than by gene or<abstract abstract-type="main" id="eos12007-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Our previous study showed that p53 protein is accumulated in &gt;60% of cases of oral squamous cell carcinoma (OSCC) and its overexpression is related to poor prognosis. However, the mechanism behind this is still elusive. The present study attempts to dissect p53 alterations at various levels from gene to function in tumor biopsies to understand whether molecular alterations have any relationship with the accumulation of p53 protein in OSCC. Protein‐stabilizing mutations were observed in only 13.8% of the samples. Neither p53 polymorphisms nor human papillomavirus (HPV) infection (&lt;2%) has any major role in augmented expression of p53 protein. Analysis of the p53 transcript demonstrated that alteration in the level of <italic>p53 </italic>mRNA (10%) is not the major mechanistic cause for accumulation of p53 protein, and p21 transcript status showed that the overexpressed p53 protein is functionally inactive. Immunoprecipitation studies demonstrated that the known interactors of p53, such as MDM2 and HSP70, have no significant role in stabilizing p53 and the significant presence of some unknown interactors, sequestering p53, and leading to the aberrant accumulation of p53. Our study suggests that overexpression of inactive p53 protein could be manifested as a result of sequestering from degradation by an unknown interacting protein rather than by gene or transcript level of alteration.</p> </abstract> … (more)
- Is Part Of:
- European journal of oral sciences. Volume 121:Number 1(2013:Feb.)Part 1
- Journal:
- European journal of oral sciences
- Issue:
- Volume 121:Number 1(2013:Feb.)Part 1
- Issue Display:
- Volume 121, Issue 1, Part 1 (2013)
- Year:
- 2013
- Volume:
- 121
- Issue:
- 1
- Part:
- 1
- Issue Sort Value:
- 2013-0121-0001-0001
- Page Start:
- 21
- Page End:
- 28
- Publication Date:
- 2012-11-30
- Subjects:
- Dentistry -- Periodicals
Oral medicine -- Periodicals
617.6005 - Journal URLs:
- http://www.blackwell-synergy.com/loi/eos ↗
http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=eos ↗
http://onlinelibrary.wiley.com/ ↗
http://firstsearch.oclc.org ↗ - DOI:
- 10.1111/eos.12007 ↗
- Languages:
- English
- ISSNs:
- 0909-8836
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3829.733250
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 2992.xml