Department of Oncology, Collegium Medicum, University of Warmia and Mazury, 10-228, Olsztyn, Poland.
Department of Oncology and Immuno-Oncology, Warmian-Masurian Cancer Center of the Ministry of the Interior and Administration Hospital, 10-228, Olsztyn, Poland.
J Cancer Res Clin Oncol. 2023 Aug;149(9):5803-5822. doi: 10.1007/s00432-022-04540-x. Epub 2022 Dec 30.
Neuropeptide Y (NPY) is a pleiotropic peptide, which is involved in many biological mechanisms important in regulation of cell growth and survival. The aim of this study was a comprehensive analysis of the NPY system in prostate pathology.
The study was based on immunohistochemical analysis of NPY and its receptors, Y1R, Y2R and Y5R, in tissue samples from benign prostate (BP), primary prostate cancer (PCa) and PCa bone metastases. Tissue microarray (TMA) technique was employed, with analysis of multiple cores from each specimen. Intensity of the immunoreactivity and expression index (EI), as well as distribution of the immunostaining in neoplastic cells and stromal elements were evaluated. Perineural invasion (PNI) and extraprostatic extension (EPE) were areas of special interests. Moreover, a transwell migration assay on the LNCaP PCa cell line was used to assess the chemotactic properties of NPY.
Morphological analysis revealed homogeneous membrane and cytoplasmic pattern of NPY staining in cancer cells and its membrane localization with apical accentuation in BP glands. All elements of the NPY system were upregulated in pre-invasive prostate intraepithelial neoplasia, PCa and metastases. EI and staining intensity of NPY receptors were significantly higher in PCa then in BP with correlation between Y2R and Y5R. The strength of expression of the NPY system was further increased in the PNI and EPE areas. In bone metastases, Y1R and Y5R presented high expression scores.
The results of our study suggest that the NPY system is involved in PCa, starting from early stages of its development to disseminated states of the disease, and participates in the invasion of PCa into the auto and paracrine matter.
神经肽 Y(NPY)是一种多效肽,参与许多重要的细胞生长和存活调节的生物学机制。本研究的目的是全面分析前列腺病理学中的 NPY 系统。
本研究基于组织样本中 NPY 及其受体 Y1R、Y2R 和 Y5R 的免疫组织化学分析,这些组织样本来自良性前列腺(BP)、原发性前列腺癌(PCa)和 PCa 骨转移。采用组织微阵列(TMA)技术,对每个标本的多个核心进行分析。评估免疫反应强度和表达指数(EI),以及免疫染色在肿瘤细胞和基质成分中的分布。神经周围侵犯(PNI)和前列腺外延伸(EPE)是特别关注的领域。此外,还使用 LNCaP PCa 细胞系的 Transwell 迁移分析来评估 NPY 的趋化特性。
形态学分析显示,NPY 在癌细胞中的膜和细胞质染色呈均匀模式,在 BP 腺体内呈膜定位,并在上皮细胞的顶端有增强。NPY 系统的所有成分在前列腺上皮内瘤变、PCa 和转移前均上调。与 BP 相比,PCa 中的 NPY 受体 EI 和染色强度显著更高,且 Y2R 和 Y5R 之间存在相关性。在 PNI 和 EPE 区域,NPY 系统的表达强度进一步增加。在骨转移中,Y1R 和 Y5R 呈现高表达评分。
我们的研究结果表明,NPY 系统参与了 PCa 的发生,从疾病早期发展到播散状态,并参与了 PCa 对自体和旁分泌物质的侵袭。