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一种用于研究非黑色素瘤皮肤癌神经侵袭的新型体外病理模型。

A Novel In Vitro Pathological Model for Studying Neural Invasion in Non-Melanoma Skin Cancer.

作者信息

Ávila-Fernández Paula, Etayo-Escanilla Miguel, Sánchez-Porras David, Blanco-Elices Cristina, Campos Fernando, Carriel Víctor, García-García Óscar Darío, Chato-Astrain Jesús

机构信息

Tissue Engineering Group, Department of Histology, Faculty of Medicine, University of Granada, 18016 Granada, Spain.

Instituto de Investigación Biosanitaria (ibs.GRANADA), 18012 Granada, Spain.

出版信息

Gels. 2024 Apr 8;10(4):252. doi: 10.3390/gels10040252.

Abstract

Neural Invasion (NI) is a key pathological feature of cancer in the colonization of distant tissues, and its underlying biological mechanisms are still scarcely known. The complex interactions between nerve and tumor cells, along with the stroma, make it difficult to reproduce this pathology in effective study models, which in turn has limited the understanding of NI pathogenesis. In this study, we have designed a three-dimensional model of NI squamous cell carcinoma combining human epidermoid carcinoma cells (hECCs) with a complete peripheral nerve segment encapsulated in a fibrine-agarose hydrogel. We recreated two vital processes of NI: a pre-invasive NI model in which hECCs were seeded on the top of the nerve-enriched stroma, and an invasive NI model in which cancer cells were immersed with the nerve in the hydrogel. Histological, histochemical and immunohistochemical analyses were performed to validate the model. Results showed that the integration of fibrin-agarose advanced hydrogel with a complete nerve structure and hECCs successfully generated an environment in which tumor cells and nerve components coexisted. Moreover, this model correctly preserved components of the neural extracellular matrix as well as allowing the proliferation and migration of cells embedded in hydrogel. All these results suggest the suitability of the model for the study of the mechanisms underlaying NI.

摘要

神经侵袭(NI)是癌症在远处组织定植中的关键病理特征,其潜在的生物学机制仍鲜为人知。神经与肿瘤细胞以及基质之间复杂的相互作用,使得在有效的研究模型中重现这种病理情况变得困难,这反过来又限制了对NI发病机制的理解。在本研究中,我们设计了一种NI鳞状细胞癌的三维模型,将人表皮样癌细胞(hECCs)与包裹在纤维蛋白-琼脂糖水凝胶中的完整外周神经段相结合。我们重现了NI的两个重要过程:一个是预侵袭性NI模型,其中hECCs接种在富含神经的基质顶部;另一个是侵袭性NI模型,其中癌细胞与水凝胶中的神经相互浸润。进行了组织学、组织化学和免疫组织化学分析以验证该模型。结果表明,纤维蛋白-琼脂糖高级水凝胶与完整神经结构和hECCs的整合成功地产生了一种肿瘤细胞与神经成分共存的环境。此外,该模型正确地保留了神经细胞外基质的成分,并允许水凝胶中嵌入的细胞增殖和迁移。所有这些结果表明该模型适用于研究NI的潜在机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf8/11049316/30e8c776d257/gels-10-00252-g001.jpg

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