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胰腺导管内乳头状黏液性肿瘤伴高级别异型增生时,幼稚神经细胞的密度达到高峰。

Peak density of immature nerve cells occurs with high-grade dysplasia in intraductal papillary mucinous neoplasms of the pancreas.

机构信息

Section of Surgical Sciences, Vanderbilt University School of Medicine, Nashville, TN, USA.

Epithelial Biology Center, Vanderbilt University School of Medicine, Nashville, TN, USA.

出版信息

J Pathol. 2022 Sep;258(1):69-82. doi: 10.1002/path.5978. Epub 2022 Jul 18.

DOI:10.1002/path.5978
PMID:35686747
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9378585/
Abstract

The development of neural structures within tumors is now considered vital for carcinogenesis. However, the time course of this development in human pre-invasive neoplasia has been incompletely described. Therefore, we performed a detailed analysis of nerves across the neoplastic spectrum in resected intraductal papillary mucinous neoplasms (IPMNs) of the pancreas. Histology and multiplexed immunochemistry demonstrated that nerve density increased from low-grade (LG) to high-grade dysplasia (HG) but did not further increase once invasive IPMN (INV IPMN) was present. Higher nerve density correlated with increasing expression of nerve growth factor (NGF) by the tumor cells. Intra-tumoral nerves were immature and lacked markers of sympathetic, parasympathetic, and sensory lineages. Here, we show for the first time the presence of neural precursor cells (NPCs) within the stroma of pancreatic tumors. The density of these doublecortin (DCX)-positive NPCs increased from LG to HG, but not from HG to INV IPMN. We conclude that peak neural density of tumors is reached in high-grade dysplasia (often termed carcinoma in situ) rather than after invasion. These findings suggest that nerve-tumor interactions are important in IPMN progression and may serve as the basis for future mechanistic studies and novel therapeutic modalities. © 2022 The Pathological Society of Great Britain and Ireland.

摘要

肿瘤内神经结构的发育现在被认为对癌发生至关重要。然而,人类癌前病变中这种发育的时间过程尚未得到充分描述。因此,我们对切除的胰腺导管内乳头状黏液性肿瘤(IPMN)中整个肿瘤谱的神经进行了详细分析。组织学和多重免疫化学显示,神经密度从低级别(LG)到高级别异型增生(HG)增加,但一旦存在侵袭性 IPMN(INV IPMN),则不会进一步增加。较高的神经密度与肿瘤细胞中神经生长因子(NGF)的表达增加相关。肿瘤内神经不成熟,缺乏交感神经、副交感神经和感觉谱系的标志物。在这里,我们首次显示了胰腺肿瘤基质中存在神经前体细胞(NPC)。这些双皮质素(DCX)阳性 NPC 的密度从 LG 增加到 HG,但从 HG 增加到 INV IPMN 则没有增加。我们得出的结论是,肿瘤的神经密度峰值出现在高级别异型增生(通常称为原位癌)中,而不是在侵袭后。这些发现表明,神经-肿瘤相互作用在 IPMN 进展中很重要,可能为未来的机制研究和新的治疗模式提供基础。2022 年英国和爱尔兰病理学学会。

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