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TMPRSS2-ERG 重排在前位优势前列腺肿瘤中的发生率及与 ERG 免疫组化的相关性。

TMPRSS2-ERG rearrangement in dominant anterior prostatic tumours: incidence and correlation with ERG immunohistochemistry.

机构信息

Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, NY, USA.

出版信息

Histopathology. 2013 Aug;63(2):279-86. doi: 10.1111/his.12153. Epub 2013 May 23.

DOI:10.1111/his.12153
PMID:23701505
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3723763/
Abstract

AIM

To study prostate cancer zonal differences in TMPRSS2-ERG gene rearrangement.

METHODS AND RESULTS

We examined 136 well-characterized dominant anterior prostatic tumours, including 61 transition zone (TZ) and 75 anterior peripheral zone (PZ) lesions, defined using strict anatomical considerations. TMPRSS2-ERG FISH and ERG protein immunohistochemistry were performed on tissue microarrays. FISH results, available for 56 TZ and 71 anterior PZ samples, were correlated with ERG staining and TZ-associated 'clear cell' histology. Fewer TZ cancers (four of 56; 7%) were rearranged than anterior PZ cancers (18 of 71; 25%) (P = 0.009); deletion was the sole mechanism of TZ cancer rearrangement. ERG protein overexpression was present in 4% (two of 56; both FISH+) and 30% (21 of 71; 17 FISH+) of TZ and anterior PZ tumours, respectively. 'Clear cell' histology was present in 21 of 56 (38%) TZ and eight of 71 (11%) anterior PZ tumours. Seven per cent of cancers with and 21% without this histology had rearrangement, regardless of zonal origin.

CONCLUSIONS

TMPRSS2-ERG rearrangement occurs in dominant TZ and anterior PZ prostate cancers, with all rearranged TZ cancers in this cohort showing deletion. ERG immunohistochemistry demonstrated excellent sensitivity (86%) and specificity (96%) for TMPRSS2-ERG rearrangement. TMPRSS2-ERG fusion is rare in TZ tumours and present at a low frequency in tumours displaying 'clear cell' histology.

摘要

目的

研究 TMPRSS2-ERG 基因重排在前列腺癌中的区带差异。

方法和结果

我们检查了 136 个特征明确的优势前叶前列腺肿瘤,包括 61 个移行区(TZ)和 75 个前周缘区(PZ)病变,这些病变是根据严格的解剖学考虑定义的。对组织微阵列进行了 TMPRSS2-ERG FISH 和 ERG 蛋白免疫组织化学检测。FISH 结果可用于 56 个 TZ 和 71 个前 PZ 样本,并与 ERG 染色和 TZ 相关的“透明细胞”组织学相关。TZ 癌的重排比例(56 例中有 4 例,7%)低于前 PZ 癌(71 例中有 18 例,25%)(P=0.009);缺失是 TZ 癌重排的唯一机制。ERG 蛋白过表达分别存在于 4%(56 例中有 2 例,均为 FISH+)和 30%(71 例中有 21 例,17 例为 FISH+)的 TZ 和前 PZ 肿瘤中。21%(56 例中有 21 例)和 8%(71 例中有 8 例)的 TZ 和前 PZ 肿瘤分别存在“透明细胞”组织学。有和没有这种组织学的癌症中,7%有重排,而与区带起源无关。

结论

TMPRSS2-ERG 重排在优势 TZ 和前 PZ 前列腺癌中发生,本队列中所有重排的 TZ 癌均显示缺失。ERG 免疫组织化学检测对 TMPRSS2-ERG 重排具有优异的敏感性(86%)和特异性(96%)。TZ 肿瘤中 TMPRSS2-ERG 融合罕见,表现为“透明细胞”组织学的肿瘤频率较低。

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