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施万细胞诱导口腔鳞状细胞癌分散中 BDNF-TRKB 相互作用的调制。

Modulation of BDNF-TRKB Interactions on Schwann Cell-induced Oral Squamous Cell Carcinoma Dispersion .

机构信息

Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, FL, U.S.A.

Department of Neurological Surgery, University of Indianapolis School of Medicine, Indianapolis, IA, U.S.A.

出版信息

Anticancer Res. 2019 Nov;39(11):5933-5942. doi: 10.21873/anticanres.13798.

Abstract

BACKGROUND/AIM: Perineural invasion (PNI) is a significant pathological feature in head and neck cancer. The molecular mechanisms of PNI are poorly understood. Contrary to the previous belief that cancer cells invade nerves, recent studies have shown that Schwann cells (SC) can dedifferentiate, intercalate between cancer cells, and promote cancer dispersion. Communication between cells through brain-derived neurotrophic factor (BDNF) activation of its receptor tropomyosin receptor kinase B (TRKB) may contribute to these cellular events. We aimed to determine the effect of TRKB inhibitor ANA-12 on the direction of cell migration and degree of SC-induced oral cancer cell dispersion.

MATERIALS AND METHODS

Cell migration and dispersion assays were performed in vitro using murine SC and oral carcinoma cell lines. Assays were performed with and without ANA-12.

RESULTS

Although SCs preferentially migrated towards cancer cells in control medium, there was minimal SC-associated cancer cell dispersion. In contrast, treatment with ANA-12 reduced migration of SCs and cancer cells towards each other and initiated more SC-associated cancer cell dispersion.

CONCLUSION

This pilot study shows that BDNF-TRKB signaling may have a role in regulating interactions between SC and oral cancer cells that affect cell migration, intercalation, and cancer cell dispersion. Further research into these interactions may provide important clues about the molecular and cellular mechanisms of PNI.

摘要

背景/目的:神经周围侵犯(PNI)是头颈部癌症的一个重要病理特征。PNI 的分子机制尚未完全阐明。与之前认为癌细胞侵犯神经的观点相反,最近的研究表明,施万细胞(SCs)可以去分化,插入癌细胞之间,并促进癌细胞扩散。细胞之间通过脑源性神经营养因子(BDNF)激活其受体原肌球蛋白受体激酶 B(TRKB)的通讯可能促成这些细胞事件。我们旨在确定 TRKB 抑制剂 ANA-12 对细胞迁移方向和 SC 诱导口腔癌细胞分散程度的影响。

材料和方法

在体外使用鼠源 SC 和口腔癌细胞系进行细胞迁移和分散测定。在有和没有 ANA-12 的情况下进行测定。

结果

尽管 SC 在对照培养基中优先向癌细胞迁移,但 SC 相关的癌细胞分散很少。相比之下,用 ANA-12 处理可减少 SC 和癌细胞之间的迁移,并启动更多的 SC 相关的癌细胞分散。

结论

这项初步研究表明,BDNF-TRKB 信号可能在调节 SC 和口腔癌细胞之间的相互作用中发挥作用,这些相互作用影响细胞迁移、插入和癌细胞分散。对这些相互作用的进一步研究可能为 PNI 的分子和细胞机制提供重要线索。

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