Literature DB >> 8158773

Immunohistochemical determination of p53 protein nuclear accumulation in prostatic adenocarcinoma.

A G Aprikian1, A S Sarkis, W R Fair, Z F Zhang, Z Fuks, C Cordon-Cardo.   

Abstract

Abnormalities of the TP53 gene are currently the most common genetic alterations associated with human malignancy. The study of altered patterns of p53 protein expression in primary prostate cancer has to date yielded a much lower incidence of alteration compared to bladder, colon, lung and breast cancer. However, the analysis of prostate cancer metastases has been limited. The objective of our study was to determine the prevalence of p53 nuclear accumulation in primary, metastatic and hormone refractory prostatic adenocarcinoma, and to characterize its relationship with conventional clinicopathological variables. We used 2 antibodies (mouse monoclonal PAb 1801 and rabbit polyclonal CM-1) and an immunohistochemical method in 93 paraffin embedded tumors (48 primary tumors, 29 lymph node metastases and 16 bone metastases) to assess p53 nuclear accumulation. Overall, p53 nuclear accumulation was observed in 19 tumors (20%), including 17 with PAb 1801 and CM-1 immunoreactivities, and 2 with CM-1 immunoreactivity only. The pattern of p53 immunoreactivity was heterogeneous in most tumors, with only 3 cases exhibiting homogeneous staining. Primary, lymph node and bone metastases exhibited p53 nuclear staining in 9 of 48 (19%), 2 of 29 (7%) and 8 of 16 (50%) cases, respectively (p = 0.003). In 6 of 10 primary hormone refractory tumors (60%) and in 3 of 38 primary hormone naive tumors (8%) p53 nuclear immunoreactivity was expressed (p = 0.002). P53 nuclear accumulation was significantly more common in higher grade primary tumors (p = 0.007). Our results suggest that p53 nuclear accumulation is relatively uncommon in prostate cancer. However, p53 nuclear accumulation appears to be associated with advanced stages of disease, as illustrated by its relatively higher occurrence in hormone refractory tumors and bone metastases. Furthermore, the significantly greater prevalence of p53 accumulation in bone metastases is currently the highest reported for prostate cancer.

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Year:  1994        PMID: 8158773     DOI: 10.1016/s0022-5347(17)35231-x

Source DB:  PubMed          Journal:  J Urol        ISSN: 0022-5347            Impact factor:   7.450


  13 in total

1.  Silencing of CD24 Enhances the PRIMA-1-Induced Restoration of Mutant p53 in Prostate Cancer Cells.

Authors:  Wei Zhang; Bin Yi; Chao Wang; Dongquan Chen; Sejong Bae; Shi Wei; Rong-Jun Guo; Changming Lu; Lisa L H Nguyen; Wei-Hsiung Yang; James W Lillard; Xingyi Zhang; Lizhong Wang; Runhua Liu
Journal:  Clin Cancer Res       Date:  2015-12-28       Impact factor: 12.531

Review 2.  Molecular markers for prostate cancer metastasis. Developing diagnostic methods for predicting the aggressiveness of prostate cancer.

Authors:  J T Isaacs
Journal:  Am J Pathol       Date:  1997-05       Impact factor: 4.307

3.  Prognostic significance of Bcl-2 in clinically localized prostate cancer.

Authors:  L Bubendorf; G Sauter; H Moch; P Jordan; A Blöchlinger; T C Gasser; M J Mihatsch
Journal:  Am J Pathol       Date:  1996-05       Impact factor: 4.307

4.  Detection of apoptosis by the TUNEL technique in clinically localised prostatic cancer before and after combined endocrine therapy.

Authors:  M Colecchia; B Frigo; C Del Boca; A Guardamagna; A Zucchi; D Colloi; O Leopardi
Journal:  J Clin Pathol       Date:  1997-05       Impact factor: 3.411

Review 5.  Molecular biology of prostate cancer.

Authors:  X B Shi; P H Gumerlock; R W deVere White
Journal:  World J Urol       Date:  1996       Impact factor: 4.226

6.  Prostate cancer in a transgenic mouse.

Authors:  N M Greenberg; F DeMayo; M J Finegold; D Medina; W D Tilley; J O Aspinall; G R Cunha; A A Donjacour; R J Matusik; J M Rosen
Journal:  Proc Natl Acad Sci U S A       Date:  1995-04-11       Impact factor: 11.205

7.  Cytokine genetic polymorphisms and prostate cancer aggressiveness.

Authors:  Jovanny Zabaleta; L Joseph Su; Hui-Yi Lin; Rosa A Sierra; M Craig Hall; A Oliver Sartor; Peter E Clark; Jennifer J Hu; Augusto C Ochoa
Journal:  Carcinogenesis       Date:  2009-05-27       Impact factor: 4.944

8.  Antisense MDM2 enhances E2F1-induced apoptosis and the combination sensitizes androgen-sensitive [corrected] and androgen-insensitive [corrected] prostate cancer cells to radiation.

Authors:  Thirupandiyur S Udayakumar; Paul Hachem; Mansoor M Ahmed; Sudhir Agrawal; Alan Pollack
Journal:  Mol Cancer Res       Date:  2008-11       Impact factor: 5.852

9.  Correlation of transcription of MALAT-1, a novel noncoding RNA, with deregulated expression of tumor suppressor p53 in small DNA tumor virus models.

Authors:  Liesl K Jeffers; Kaiwen Duan; Lesley G Ellies; William T Seaman; Raquel A Burger-Calderon; Luda B Diatchenko; Jennifer Webster-Cyriaque
Journal:  J Cancer Ther       Date:  2013-05

10.  Androgen receptor expression in relation to apoptosis and the expression of cell cycle related proteins in prostate cancer.

Authors:  Zahra Amirghofran; Ahmad Monabati; Naser Gholijani
Journal:  Pathol Oncol Res       Date:  2004-03-18       Impact factor: 3.201

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