Clinical significance of p53 alterations in surgically treated prostate cancers.

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Clinical significance of p53 alterations in surgically treated prostate cancers. / Schlomm, Thorsten; Iwers, Liv; Kirstein, Patrick; Jessen, Birte; Köllermann, Jens; Minner, Sarah; Passow-Drolet, Annika; Mirlacher, Martina; Milde-Langosch, Karin; Graefen, Markus; Haese, Alexander; Steuber, Thomas; Simon, Ronald; Huland, Hartwig; Sauter, Guido; Erbersdobler, Andreas.

In: MODERN PATHOL, Vol. 21, No. 11, 11, 2008, p. 1371-1378.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Schlomm, T, Iwers, L, Kirstein, P, Jessen, B, Köllermann, J, Minner, S, Passow-Drolet, A, Mirlacher, M, Milde-Langosch, K, Graefen, M, Haese, A, Steuber, T, Simon, R, Huland, H, Sauter, G & Erbersdobler, A 2008, 'Clinical significance of p53 alterations in surgically treated prostate cancers.', MODERN PATHOL, vol. 21, no. 11, 11, pp. 1371-1378. <http://www.ncbi.nlm.nih.gov/pubmed/18552821?dopt=Citation>

APA

Schlomm, T., Iwers, L., Kirstein, P., Jessen, B., Köllermann, J., Minner, S., Passow-Drolet, A., Mirlacher, M., Milde-Langosch, K., Graefen, M., Haese, A., Steuber, T., Simon, R., Huland, H., Sauter, G., & Erbersdobler, A. (2008). Clinical significance of p53 alterations in surgically treated prostate cancers. MODERN PATHOL, 21(11), 1371-1378. [11]. http://www.ncbi.nlm.nih.gov/pubmed/18552821?dopt=Citation

Vancouver

Schlomm T, Iwers L, Kirstein P, Jessen B, Köllermann J, Minner S et al. Clinical significance of p53 alterations in surgically treated prostate cancers. MODERN PATHOL. 2008;21(11):1371-1378. 11.

Bibtex

@article{8f9533d154d34aa4adaa0342c0dcf708,
title = "Clinical significance of p53 alterations in surgically treated prostate cancers.",
abstract = "Despite the high number of previous studies, the role of p53 alterations in prostate cancer is not clearly defined. To address the role of p53 alterations in prostate cancer biology, a total of 2514 cancers treated by radical prostatectomy were successfully analyzed by immunohistochemistry in a tissue microarray format. Overall a low rate of p53-positive tumors was found (2.5%). A significant underestimation of p53-positive cases was excluded by subsequent large section analyses and direct sequencing of the p53 gene in subsets of our patients. Large section analysis of 23 cases considered negative on the tissue microarray yielded only one weakly p53-positive tumor. Only 4 out of 64 (6.4%) high-grade tumors, that were considered negative for p53 by immunohistochemistry, presented exon 5-8 mutations. These data suggest a high sensitivity of our immunohistochemistry approach and confirm the overall low frequency of p53 alterations in clinically localized prostate cancer. A positive p53 immunostaining was strongly associated with presence of exon 5-8 mutations (P",
author = "Thorsten Schlomm and Liv Iwers and Patrick Kirstein and Birte Jessen and Jens K{\"o}llermann and Sarah Minner and Annika Passow-Drolet and Martina Mirlacher and Karin Milde-Langosch and Markus Graefen and Alexander Haese and Thomas Steuber and Ronald Simon and Hartwig Huland and Guido Sauter and Andreas Erbersdobler",
year = "2008",
language = "Deutsch",
volume = "21",
pages = "1371--1378",
journal = "MODERN PATHOL",
issn = "0893-3952",
publisher = "NATURE PUBLISHING GROUP",
number = "11",

}

RIS

TY - JOUR

T1 - Clinical significance of p53 alterations in surgically treated prostate cancers.

AU - Schlomm, Thorsten

AU - Iwers, Liv

AU - Kirstein, Patrick

AU - Jessen, Birte

AU - Köllermann, Jens

AU - Minner, Sarah

AU - Passow-Drolet, Annika

AU - Mirlacher, Martina

AU - Milde-Langosch, Karin

AU - Graefen, Markus

AU - Haese, Alexander

AU - Steuber, Thomas

AU - Simon, Ronald

AU - Huland, Hartwig

AU - Sauter, Guido

AU - Erbersdobler, Andreas

PY - 2008

Y1 - 2008

N2 - Despite the high number of previous studies, the role of p53 alterations in prostate cancer is not clearly defined. To address the role of p53 alterations in prostate cancer biology, a total of 2514 cancers treated by radical prostatectomy were successfully analyzed by immunohistochemistry in a tissue microarray format. Overall a low rate of p53-positive tumors was found (2.5%). A significant underestimation of p53-positive cases was excluded by subsequent large section analyses and direct sequencing of the p53 gene in subsets of our patients. Large section analysis of 23 cases considered negative on the tissue microarray yielded only one weakly p53-positive tumor. Only 4 out of 64 (6.4%) high-grade tumors, that were considered negative for p53 by immunohistochemistry, presented exon 5-8 mutations. These data suggest a high sensitivity of our immunohistochemistry approach and confirm the overall low frequency of p53 alterations in clinically localized prostate cancer. A positive p53 immunostaining was strongly associated with presence of exon 5-8 mutations (P

AB - Despite the high number of previous studies, the role of p53 alterations in prostate cancer is not clearly defined. To address the role of p53 alterations in prostate cancer biology, a total of 2514 cancers treated by radical prostatectomy were successfully analyzed by immunohistochemistry in a tissue microarray format. Overall a low rate of p53-positive tumors was found (2.5%). A significant underestimation of p53-positive cases was excluded by subsequent large section analyses and direct sequencing of the p53 gene in subsets of our patients. Large section analysis of 23 cases considered negative on the tissue microarray yielded only one weakly p53-positive tumor. Only 4 out of 64 (6.4%) high-grade tumors, that were considered negative for p53 by immunohistochemistry, presented exon 5-8 mutations. These data suggest a high sensitivity of our immunohistochemistry approach and confirm the overall low frequency of p53 alterations in clinically localized prostate cancer. A positive p53 immunostaining was strongly associated with presence of exon 5-8 mutations (P

M3 - SCORING: Zeitschriftenaufsatz

VL - 21

SP - 1371

EP - 1378

JO - MODERN PATHOL

JF - MODERN PATHOL

SN - 0893-3952

IS - 11

M1 - 11

ER -