Journal article
Nuclear MTA1 overexpression is associated with aggressive prostate cancer, recurrence and metastasis in African Americans
Scientific reports, Vol.3(1), pp.2331-2331
2013
DOI: 10.1038/srep02331
PMCID: PMC3728596
PMID: 23900262
Abstract
Metastasis-associated protein 1 (MTA1), a negative epigenetic modifier, plays a critical role in prostate cancer (PCa) progression. We hypothesized that MTA1 overexpression in primary tumor tissues can predict PCa aggressiveness and metastasis. Immunohistochemical staining of MTA1 was done on archival PCa specimens from University of Mississippi Medical Center and University of Iowa. We found that nuclear MTA1 overexpression was positively correlated with the severity of disease progression reaching its highest levels in metastatic PCa. Nuclear MTA1 overexpression was significantly associated with Gleason > 7 tumors in African Americans but not in Caucasians. It was also a predictor of recurrent disease. We concluded that MTA1 nuclear overexpression may be a prognostic indicator and a future therapeutic target for aggressive PCa in African American men. Our findings may be useful for categorizing African American patients with a higher probability of recurrent disease and metastasis from those who are likely to remain metastasis-free.
Details
- Title: Subtitle
- Nuclear MTA1 overexpression is associated with aggressive prostate cancer, recurrence and metastasis in African Americans
- Creators
- Steven J Dias - University of Mississippi Medical CenterXinchun Zhou - University of Mississippi Medical CenterMarina Ivanovic - University of IowaMichael P Gailey - University of IowaSwati Dhar - University of Mississippi Medical CenterLiangfen Zhang - University of Mississippi Medical CenterZhi He - University of Mississippi Medical CenterAlan D Penman - University of Mississippi Medical CenterSrinivasan Vijayakumar - University of Mississippi Medical CenterAnait S Levenson - University of Mississippi Medical Center
- Resource Type
- Journal article
- Publication Details
- Scientific reports, Vol.3(1), pp.2331-2331
- DOI
- 10.1038/srep02331
- PMID
- 23900262
- PMCID
- PMC3728596
- NLM abbreviation
- Sci Rep
- ISSN
- 2045-2322
- eISSN
- 2045-2322
- Publisher
- Nature Publishing Group
- Language
- English
- Date published
- 2013
- Academic Unit
- Pathology
- Record Identifier
- 9984201258402771
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