Up-regulation of Biglycan is Associated with Poor Prognosis and PTEN Deletion in Patients with Prostate Cancer

被引:54
作者
Jacobsen, Frank [1 ]
Kraft, Juliane [1 ]
Schroeder, Cornelia [2 ]
Hube-Magg, Claudia [1 ]
Kluth, Martina [1 ]
Lang, Dagmar S. [1 ]
Simon, Ronald [1 ]
Sauter, Guido [1 ]
Izbicki, Jakob R. [2 ]
Clauditz, Till S. [1 ]
Luebke, Andreas M. [1 ]
Hinsch, Andrea [1 ]
Wilczak, Waldemar [1 ]
Wittmer, Corinna [1 ]
Buescheck, Franziska [1 ]
Hoeflmayer, Doris [1 ]
Minner, Sarah [1 ]
Tsourlakis, Maria Christina [1 ]
Huland, Hartwig [3 ]
Graefen, Markus [3 ]
Budaeus, Lars [3 ]
Thederan, Imke [3 ]
Salomon, Georg [3 ,4 ]
Schlomm, Thorsten [3 ]
Melling, Nathaniel [2 ]
机构
[1] Univ Med Ctr Hamburg Eppendorf, Inst Pathol, Martinistr 52, D-20246 Hamburg, Germany
[2] Univ Med Ctr Hamburg Eppendorf, Gen Visceral & Thorac Surg Dept & Clin, Hamburg, Germany
[3] Univ Med Ctr Hamburg Eppendorf, Prostate Canc Ctr, Martini Clin, Hamburg, Germany
[4] Univ Med Ctr Hamburg Eppendorf, Sect Translat Prostate Canc Res, Dept Urol, Hamburg, Germany
来源
NEOPLASIA | 2017年 / 19卷 / 09期
关键词
EXTRACELLULAR-MATRIX PROTEINS; EARLY PSA RECURRENCE; ANDROGEN RECEPTOR; GENOMIC DELETION; CORE PROTEIN; EXPRESSION; PROTEOGLYCANS; PATHWAY; FUSION; TRANSCRIPTION;
D O I
10.1016/j.neo.2017.06.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Biglycan (BGN), a proteoglycan of the extracellular matrix, is included in mRNA signatures for prostate cancer aggressiveness. To understand the impact of BGN on prognosis and its relationship to molecularly defined subsets, we analyzed BGN expression by immunohistochemistry on a tissue microarray containing 12,427 prostate cancers. Seventy-eight percent of 11,050 interpretable cancers showed BGN expression, which was considered as low intensity in 47.7% and as high intensity in 31.1% of cancers. BGN protein expression rose with increasing pathological tumor stage, Gleason grade, lymph node metastasis and early PSA recurrence (P < .0001 each). Comparison with our molecular database attached to the TMA revealed that BGN expression was linked to presence of TMPRRS2: ERG fusion and PTEN deletion (P < .0001 each). In addition, BGN was strongly linked to androgen-receptor (AR) levels (P < .0001), suggesting a hormone-depending regulation of BGN. BGN up-regulation is a frequent feature of prostate cancer that parallels tumor progression and may be useful to estimate tumor aggressiveness particularly if combined with other molecular markers.
引用
收藏
页码:707 / 715
页数:9
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