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口腔肿瘤细胞外泌体 miR-10b 通过 AKT 信号通路刺激细胞侵袭和迁移。

The Oral Tumor Cell Exosome miR-10b Stimulates Cell Invasion and Relocation via AKT Signaling.

机构信息

Department of Stomatology, Huangshi Central Hospital, Affiliated Hospital of Hubei Polytechnic University, Edong Healthcare Group, Huangshi 435000, China.

Department of Dermatology, Huangshi Central Hospital, Affiliated Hospital of Hubei Polytechnic University, Edong Healthcare Group, Huangshi 435000, China.

出版信息

Contrast Media Mol Imaging. 2022 Aug 16;2022:3188992. doi: 10.1155/2022/3188992. eCollection 2022.

Abstract

An exosome derived from a cancer cell has been identified to regulate intercellular communication. However, the roles of oral cancer-derived ectodomains in tumor metastasis need to be investigated further. We investigated their roles in oral cancer cells in this paper. The enforcing effect on oral cancer cells was attributed primarily to miR-10b, a gene with a high level in exosomes that is transferred to recipient cells via oral cancer-derived exosomes. Exosomes were obtained by exosome isolation reagents. Also, exosome identification and analysis were performed by electron microscopy. The expression of miRNAs was analyzed by qRT-PCR. Protein expression was analyzed by Western blot. Also, invasion and migration experiments were performed to assay and evaluate the function of exosomal miR-10b. Exosome-mediated transfer of miR-10b promoted oral cancer cell behaviors, according to the findings. Finally, it was discovered that AKT signaling participates in regulating exosome-mediated invasion and migration of oral cancer cells and its activation reduced the inhibitory effect of miR-10b knockdown on oral cancer cells. Exosomal miR-10b derived from oral cancer cells enhances cell invasion and migration by activating AKT signaling.

摘要

已经鉴定出一种源自癌细胞的外泌体来调节细胞间通讯。然而,口腔癌衍生的胞外结构域在肿瘤转移中的作用还需要进一步研究。本文研究了它们在口腔癌细胞中的作用。通过口腔癌衍生的外泌体将其转移至受体细胞,miR-10b 基因作为一种高水平表达的基因,主要归因于外泌体对口腔癌细胞的强化作用。外泌体是通过外泌体分离试剂获得的。此外,还通过电子显微镜进行外泌体鉴定和分析。通过 qRT-PCR 分析 miRNA 的表达。通过 Western blot 分析蛋白表达。还进行了侵袭和迁移实验,以检测和评估外泌体 miR-10b 的功能。根据研究结果,外泌体介导的 miR-10b 转移促进了口腔癌细胞的行为。最后发现,AKT 信号参与调节外泌体介导的口腔癌细胞侵袭和迁移,其激活降低了 miR-10b 敲低对口腔癌细胞的抑制作用。口腔癌细胞衍生的外泌体 miR-10b 通过激活 AKT 信号增强细胞侵袭和迁移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9992/9398826/69b45fbe5fcb/CMMI2022-3188992.001.jpg

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