HOXB13 overexpression is an independent predictor of early PSA recurrence in prostate cancer treated by radical prostatectomy
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HOXB13 overexpression is an independent predictor of early PSA recurrence in prostate cancer treated by radical prostatectomy. / Zabalza, Cristina Villares; Adam, Meike; Burdelski, Christoph; Wilczak, Waldemar; Wittmer, Corinna; Kraft, Stefan; Krech, Till; Steurer, Stefan; Koop, Christina; Hube-Magg, Claudia; Graefen, Markus; Heinzer, Hans; Minner, Sarah; Simon, Ronald; Sauter, Guido; Schlomm, Thorsten; Tsourlakis, Maria Christina.
in: ONCOTARGET, Jahrgang 6, Nr. 14, 23.03.2015, S. 12822-12834.Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung
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T1 - HOXB13 overexpression is an independent predictor of early PSA recurrence in prostate cancer treated by radical prostatectomy
AU - Zabalza, Cristina Villares
AU - Adam, Meike
AU - Burdelski, Christoph
AU - Wilczak, Waldemar
AU - Wittmer, Corinna
AU - Kraft, Stefan
AU - Krech, Till
AU - Steurer, Stefan
AU - Koop, Christina
AU - Hube-Magg, Claudia
AU - Graefen, Markus
AU - Heinzer, Hans
AU - Minner, Sarah
AU - Simon, Ronald
AU - Sauter, Guido
AU - Schlomm, Thorsten
AU - Tsourlakis, Maria Christina
PY - 2015/3/23
Y1 - 2015/3/23
N2 - HOXB13 is a prostate cancer susceptibility gene which shows a cancer predisposing (G84E) mutation in 0.1-0.6% of males. We analyzed the prognostic impact of HOXB13 expression by immunohistochemistry on a tissue microarray containing more than 12,400 prostate cancers. Results were compared to tumor phenotype, biochemical recurrence, androgen receptor (AR) and prostate specific antigen (PSA) as well as molecular subtypes defined by ERG status and genomic deletions of 3p, 5q, 6q, and PTEN. HOXB13 immunostaining was detectable in 51.7% of 10,216 interpretable cancers and considered strong in 9.6%, moderate in 19.7% and weak in 22.3% of cases. HOXB13 expression was linked to advanced pT stage, high Gleason grade, positive lymph node status (p < 0.0001 each), high pre-operative PSA levels (p = 0.01), TMPRSS2:ERG fusion, PTEN deletions, AR expression, cell proliferation, reduced PSA expression and early PSA recurrence (p < 0.0001 each). The prognostic value of HOXB13 was independent from established parameters including Gleason, stage, nodal stage and PSA. Co-expression analysis identified a subset of tumors with high HOXB13 and AR but low PSA expression that had a particularly poor prognosis. HOXB13 appears to be a promising candidate for clinical routine tests either alone or in combination with other markers, including AR and PSA.
AB - HOXB13 is a prostate cancer susceptibility gene which shows a cancer predisposing (G84E) mutation in 0.1-0.6% of males. We analyzed the prognostic impact of HOXB13 expression by immunohistochemistry on a tissue microarray containing more than 12,400 prostate cancers. Results were compared to tumor phenotype, biochemical recurrence, androgen receptor (AR) and prostate specific antigen (PSA) as well as molecular subtypes defined by ERG status and genomic deletions of 3p, 5q, 6q, and PTEN. HOXB13 immunostaining was detectable in 51.7% of 10,216 interpretable cancers and considered strong in 9.6%, moderate in 19.7% and weak in 22.3% of cases. HOXB13 expression was linked to advanced pT stage, high Gleason grade, positive lymph node status (p < 0.0001 each), high pre-operative PSA levels (p = 0.01), TMPRSS2:ERG fusion, PTEN deletions, AR expression, cell proliferation, reduced PSA expression and early PSA recurrence (p < 0.0001 each). The prognostic value of HOXB13 was independent from established parameters including Gleason, stage, nodal stage and PSA. Co-expression analysis identified a subset of tumors with high HOXB13 and AR but low PSA expression that had a particularly poor prognosis. HOXB13 appears to be a promising candidate for clinical routine tests either alone or in combination with other markers, including AR and PSA.
M3 - SCORING: Journal article
C2 - 25825985
VL - 6
SP - 12822
EP - 12834
JO - ONCOTARGET
JF - ONCOTARGET
SN - 1949-2553
IS - 14
ER -