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前列腺肿瘤中的神经内分泌分化

Neuroendocrine differentiation in prostate neoplasms.

作者信息

Grobholz Rainer

机构信息

Medical Faculty, University of Zurich, Zurich, Switzerland.

Institute of Pathology, Cantonal Hospital Aarau, Tellstrasse 25, 5001, Aarau, Switzerland.

出版信息

Pathologie (Heidelb). 2025 Aug 25. doi: 10.1007/s00292-025-01449-3.

DOI:10.1007/s00292-025-01449-3
PMID:40853482
Abstract

Neuroendocrine (NE) cells in the prostate are part of the diffuse NE system and are found in both the normal prostate and acinar adenocarcinomas, occasionally exhibiting Paneth cell-like morphology.NE cells produce peptide hormones and biogenic amines that influence the differentiation and growth of the prostate glands through paracrine signaling; however, they do not show proliferative activity and lack androgen receptors (AR).Prostate tumors with NE differentiation are classified into five groups: (1) acinar adenocarcinomas with partial NE differentiation, detectable only by immunohistochemistry, (2) adenocarcinomas with Paneth cell-like differentiation, (3) NE tumors/carcinoids (NET), (4) small cell NE carcinomas (SCNEC), and (5) large cell NE carcinomas (LCNEC).The significance of partial and Paneth cell-like differentiation in adenocarcinomas remains under discussion and plays a minor role in routine diagnostics. NETs are extremely rare and appear to behave similarly to NETs of the gastrointestinal tract. In contrast, SCNECs and LCNECs are aggressive tumors with important clinical relevance, as they have a poor prognosis and require aggressive treatment.Therapy-associated neuroendocrine prostate carcinomas (t-NEPC) are recognized as a distinct entity for the first time in the WHO classification (5th edition, 2022). It arises through transdifferentiation via epigenetic changes following androgen deprivation and is characterized by AR loss and high proliferation, among other features. As with primary NE carcinomas, aggressive therapy is indicated. Therefore, a follow-up biopsy is recommended for castration-resistant progressive prostate cancer to confirm this aggressive phenotype.

摘要

前列腺中的神经内分泌(NE)细胞是弥散性NE系统的一部分,在正常前列腺和腺泡腺癌中均有发现,偶尔呈现潘氏细胞样形态。NE细胞产生肽类激素和生物胺,通过旁分泌信号影响前列腺腺管的分化和生长;然而,它们不表现出增殖活性且缺乏雄激素受体(AR)。具有NE分化的前列腺肿瘤分为五组:(1)仅通过免疫组织化学可检测到的部分NE分化的腺泡腺癌,(2)具有潘氏细胞样分化的腺癌,(3)NE肿瘤/类癌(NET),(4)小细胞NE癌(SCNEC),以及(5)大细胞NE癌(LCNEC)。腺癌中部分和潘氏细胞样分化的意义仍在讨论中,在常规诊断中作用较小。NET极为罕见,其行为似乎与胃肠道NET相似。相比之下,SCNEC和LCNEC是具有重要临床意义的侵袭性肿瘤,因为它们预后较差,需要积极治疗。治疗相关的神经内分泌前列腺癌(t-NEPC)在世界卫生组织分类(第5版,2022年)中首次被确认为一个独特的实体。它通过雄激素剥夺后表观遗传变化的转分化产生,其特征包括AR缺失和高增殖等。与原发性NE癌一样,需要积极治疗。因此,对于去势抵抗性进展性前列腺癌,建议进行随访活检以确认这种侵袭性表型。

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本文引用的文献

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Promising therapy for neuroendocrine prostate cancer: current status and future directions.神经内分泌前列腺癌的前景疗法:现状与未来方向
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A systematic review of primary large cell neuroendocrine carcinoma of the prostate.前列腺原发性大细胞神经内分泌癌的系统评价。
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FOXA2 is a sensitive and specific marker for small cell neuroendocrine carcinoma of the prostate.FOXA2 是前列腺小细胞神经内分泌癌的敏感且特异的标志物。
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