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含黑素瘤球体的人工真皮作为一种替代体内模型的方法。

Melanoma spheroid-containing artificial dermis as an alternative approach to in vivo models.

机构信息

Department of Chemistry, Center of Nanotechnology and Tissue Engineering -Photobiology and Photomedicine Research Group, Faculty of Philosophy, Sciences and Letters of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, 14040-901, Brazil.

Department of Cellular and Molecular Biology, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, 14049-900, Brazil.

出版信息

Exp Cell Res. 2022 Aug 1;417(1):113207. doi: 10.1016/j.yexcr.2022.113207. Epub 2022 May 14.

Abstract

Melanoma spheroid-loaded 3D skin models allow for the study of crucial tumor characteristics and factors at a superior level because the neoplastic cells are integrated into essential human skin components, permitting tumor-skin model communication. Herein, we designed a melanoma-containing artificial dermis by inserting multicellular tumor spheroids from the metastatic phase of WM 1617 melanoma cells into an artificial dermis. We cultured multicellular melanoma spheroids by hanging drop method (250 cells per drop) with a size of 420 μm in diameter after incubation for 14 days. These spheroids were integrated into the dermal equivalents that had been previously preparedwith a type-I collagen matrix and healthy fibroblasts. The melanoma spheroid cells invaded and proliferated in the artificial dermis. Spheroids treated with a 1.0 μmol/L aluminum chloride phthalocyanine nanoemulsion in the absence of light showed high cell viability. In contrast, under irradiation with visible red light (660 nm) at 25 J/cm, melanoma cells were killed and the healthy tissue was preserved, indicating that photodynamic therapy is effective in such a model. Therefore, the 3D skin melanoma model has potential to promote research in full-thickness skin model targeting optimized preclinical assays.

摘要

黑色素瘤球体负载的 3D 皮肤模型允许在更高水平上研究关键的肿瘤特征和因素,因为肿瘤细胞被整合到重要的人类皮肤成分中,允许肿瘤-皮肤模型进行通信。在这里,我们通过将转移性阶段的 WM 1617 黑色素瘤细胞的多细胞肿瘤球体插入人工真皮中来设计包含黑色素瘤的人工真皮。我们通过在 14 天后培养 420μm 直径的悬滴法(每个滴 250 个细胞)培养多细胞黑色素瘤球体。这些球体被整合到先前用 I 型胶原基质和健康成纤维细胞制备的真皮等效物中。黑色素瘤球体细胞在人工真皮中侵袭和增殖。在没有光照的情况下用 1.0μmol/L 铝酞菁纳米乳液处理的球体显示出高细胞活力。相比之下,在 660nm 的可见红光照射下(25J/cm),黑色素瘤细胞被杀死,健康组织得以保留,表明光动力疗法在这种模型中是有效的。因此,3D 皮肤黑色素瘤模型有可能促进针对优化临床前检测的全层皮肤模型的研究。

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